Cannabis Quality Assurance Technician Jobs
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Here are 41 cannabis jobs mentioning "quality assurance technician" in April 2024, at companies like Jushi, Trulieve, Cresco Labs, and VidaCann, including positions such as Quality Assurance Technician, Quality Assurance Technician - 2nd Shift, Compliance and Quality Assurance Technician, and Quality Assurance Technician 1st Shift- Cultivation (Job 1656780).
More than 30+ days
Job title: Quality Assurance Technician
Reporting Location: Tampa, FL 33610 (10 Minutes from Busch Gardens)
Key responsibilities:
- Wearing the appropriate PPE’s making sure that we are actively replacing the required PPEs in each specific situation/manufacturing room, at the correct frequency, to prevent cross contamination.
- Assures consistent quality of production by maintaining good manufacturing practice (GMP), validating all in-process checks real time, monitoring logs for accuracy and completion, documenting discrepancies, and completing accurate daily EOD reports.
- Communicating clear and real time in process updates, real status of project completion, prompt escalation of any issues.
- Teamwork, open communication, coordinate all work activities, including lunch breaks, emergencies, vacations, time off, with your peers, own your development, ask questions, take notes.
- Collaborate with manufacturing team making sure that In-process checks are being conducted in a timely manner.
Available hours: Full time Schedule
Cansortium Inc is a vertically integrated cultivator, processor, formulator, and retailer of Premium Cannabis Products
currently operating in Florida, Pennsylvania and Texas as Fluent Cannabis, as well as in Michigan through its in-market
partner. Our purpose is to compassionately provide patients access to the highest level of medical cannabis in an
unrivaled, professional healthcare environment with outstanding customer service. Patient care always comes first at
Fluent and our standards, practices, and performance is unmatched.
We are looking for leaders who want to work alongside great talent and create a positive work experience for their
team. We are focused on continuous improvements, which creates development opportunities, engaged feedback, and
increased contributions towards our goals as a leader in the medical cannabis industry.
Find out more at www.getfluent.com. Follow us on LinkedIn.
ROLE SUMMARY
A Quality Assurance Technician is responsible for assuring consistent production quality by developing and enforcing
good manufacturing practice (GMP) systems, validating processes, performing audits, handling system improvements
and providing documentation.
KEY RESPONSIBILITIES
- Assures consistent quality of production by developing and enforcing good manufacturing practice (GMP)
- Accomplishes quality assurance human resource objectives by orienting, training, assigning, scheduling,
- Achieves quality assurance operational objectives by contributing information and analysis to strategic plans and
resolving problems; completing audits; determining system improvements, implementing change and initiating
corrective actions.
- Develops quality assurance plans by conducting hazard analyses, identifying critical control points and
procedures; and monitoring inventories.
- Validates quality processes by establishing product specifications and quality attributes, measuring production,
quality assurance procedures.
- Maintains and improves product quality by completing product, company, system, compliance, and surveillance
- Collaborates with other members of management to develop new product and engineering designs, and
- Prepares quality documentation and reports by collecting, analyzing and summarizing information and trends
- Updates job knowledge by studying trends in and developments in quality management; participating in
professional organizations.
- Enhances department and organization reputation by accepting ownership for accomplishing new and different
QUALIFICATIONS
- Bachelor of Science degree or related field.
- Minimum two years of experience in a Quality Management/ Quality Control, supporting Pharmaceutical,
- GMP knowledge with a focus in operational excellence in GMPs, recalls, electronic and hard copy records in an
- Experience with QA measuring and testing equipment
- Knowledge of safety requirements and legal standards
- Working knowledge of quality system requirements
- Experience with MS Word, Excel, Project Management, and Analytics software
- Analyzing information
- Strategic planning
- Informing others
- Emphasizing excellence
- Dealing with complexity
SKILLS
- Must be a multitasker, with the ability to work on several requests simultaneously without losing focus
- Organization and initiative, good communications skills, proactive, problem-solving, time management,
- Excellent critical thinking and analytical skills
- Must possess an inquisitive and creative mind
- Ability to build good relationships. There will be frequent contact with internal, either face to face or by
- Teamwork- collaborating with others to improve overall standards of work and service
- Thoroughness
REQUIRED EDUCATION and EXPERIENCE
- Bachelor of Science degree or related field
ADDITIONAL REQUIREMENTS
Per state law, must be at least 21 years of age.
Must successfully complete a comprehensive background check.
Must pass a drug screening
SUPERVISORY RESPONSIBILITIES
This position has no supervisory responsibilities
WORK ENVIRONMENT
This position operates in cultivation and manufacturing environments. This role routinely uses cultivation processing
equipment and standard office equipment such as computers, phones, photocopiers, filing cabinets and fax machines.
PHYSICAL DEMANDS
The physical demands described here are representative of those that must be met by an employee to successfully
perform the essential functions of this job. While performing the duties of this job, the employee is regularly required to
speak and hear. The employee frequently is required to stand for extended periods; walk; use hands to handle or feel
objects, tools or controls; reach with hands and arms. Must be able to individually lift up to 25 lbs. Regular and
predictable attendance is essential.
POSITION TYPE / EXPECTED HOURS OF WORK
This position regularly requires long hours and frequent weekend work.
TRAVEL
Travel is primarily local during the business day, although some out-of-the-area and overnight travel may be expected.
OTHER DUTIES
Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or
responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any
time with or without notice.
The company will ask you to help out in other departments depending on company needs. This means that you may not
always work in the department that you were hired, teamwork and getting product out to patients is the goal and this
means helping out where you are needed is crucial to your success as well as the company’s success.
AAP/EEO Statement
Fluent is an equal opportunity employer and we welcome applications from all backgrounds regardless of race, color,
religion, sex, ancestry, age, marital status, sexual orientation, gender identity, disability or any other classification
protected by law.
COMPANY BENEFITS
Fluent provides comprehensive benefits offerings to all full-time employees. Our benefits include medical, dental and
vision and supplemental insurance, paid time-off program and non-matching 401k plan.
All applicants must be legally authorized to work in the United States and will be required to submit proof of such eligibility.
Please note: Only shortlisted candidates will be contacted
Apply for this job with Fluent Cannabis Care
Apply now →
By clicking the "Apply now" button, you'll be leaving Fazow and going to an external job application page for this company.
Please research all companies before applying. When applying for jobs, you should NOT have to pay to apply.
Fazow accepts no liability or responsibility as a consequence of any reliance upon information on external sites or in jobs listed on fazow.com.
THE TEAM:
Founded in 2018 and headquartered in Boca Raton, Florida, Jushi is a vertically integrated, multi-state cannabis company that develops and operates high-end retail locations, premium brands, state-of-the-art cultivation, processing, manufacturing facilities, along with a cutting-edge online platform that is setting a new standard for a sophisticated, data-driven, modern cannabis experience.
Since its founding in 2018, Jushi has grown from just a handful of people with an idea to more than 900 employees strong. The Company has scaled its operations in seven states, including Pennsylvania, Virginia, Massachusetts, Illinois, California, Nevada, and Ohio, and has been named one of the top five cannabis companies to work for by Cannabis Business Times.
The Company operates more than two dozen retail locations across the country under the retail brand, BEYOND / HELLO™ as well as under the recently acquired brand, Nature’s Remedy. The Company provides an unparalleled in-store experience, coupled with online reservations and in-store express pickup.
Each day, Jushi team members continue to grow, cultivate, process and manufacture a comprehensive suite of cannabis brands under the names: The Bank, The Lab, Tasteology, Nira + Medicinals and Sèche, which are addressing a wide variety of consumer and patient needs across multiple states
THE OPPORTUNITY
Want to make a meaningful difference in peoples’ lives while earning a competitive salary? At Jushi, we are shaping the future of the cannabis industry, the fastest growing jobs sector in the U.S. The Quality Assurance (QA) Technician will be responsible for assisting in all quality aspects of the production site and ensure all products are manufactured in compliance with 21CFR111 requirements. The QA Technician is responsible for quality inspections of Medical Cannabis products and auditing the processes and procedures in the medical cannabis manufacturing operation. They are required to follow set processes and ensure adherence to state regulations, SOPs, work instructions (WI), and adhere to good manufacturing practices (GMP), good laboratory practices (GLP) and other product quality standards.
WHAT YOU WILL DO
- Perform Quality Inspections on products, equipment, and procedures.
- Responsible for monitoring cannabis product quality and safety throughout the manufacturing process.
- Responsible for performing verification of sanitation, equipment and other areas as required.
- Responsible for auditing the correct recording and filing of all relevant record logs and documentation completed by staff.
- Ensures the correct guidelines for production are followed during operations.
- Ensures employees are following all SOP’s, Work Instructions, and worker safety practices.
- Assist Quality Manager with instructing employees on Quality Improvements or Issues.
- Collect product samples for Product Development, lab retains and the laboratory when directed.
- May perform or assist inventory management personnel with inventory audits when needed.
- Support team members on quality management program to ensure there is an in-depth understanding of program and individual responsibilities.
- Provide support to GMP production operations, including conducting SOPs, training, and serve as resource to operations for quality controls and GMP compliance.
- Support improvement and alignment of the Quality Management Systems at site level.
- Conduct all duties in compliance with safety rules, applicable SOPs, and other relevant guidelines.
- Support all staff in data collection and analysis, reporting activities that support quality improvement interventions, transparency, compliance regulatory standards and provide performance monitoring.
- Support review and approval of batch record documentation, including validation protocols, master batch records, analytical test results, packaging, and labeling documentation.
EDUCATION & EXPERIENCE
- Familiarity with FDA regulations and/or operating in a regulated environment preferred.
- Attention to detail and ability to record numerical data and understand nomenclature and lot/Batch numbering systems.
- Ability to be flexible and provide support to any department within the organization as required by Operations leadership.
- Must be able to read and write in English and the ability to perform basic calculations.
- Microsoft Office skills.
- Must pass criminal background check.
PHYSICAL REQUIRMENTS
- Regularly perform desk-based computer tasks
- Frequently sitting and standing
- Occasionally Twist/bend/stoop/squat, kneel/crawl
- An environment with minimal noise levels
OTHER DUTIES
Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice
Jushi is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity or expression, religion, national origin or ancestry, age, disability, marital status, pregnancy, protected veteran status, protected genetic information, political affiliation, or any other characteristics protected by local laws, regulations, or ordinances.
We offer benefit packages that may include: Medical, Dental, Vision, Life, Short, and Long Term Disability, Flexible Spending Accounts, Paid Time Off, and Paid Holidays.
Job Type: Full-time
Schedule:
- 8 hour shift
Ability to commute/relocate:
- Toledo, OH 43612: Reliably commute or planning to relocate before starting work (Required)
Experience:
- QA/QC: 1 year (Required)
Work Location: One location
Apply for this job with Jushi
Apply now →
By clicking the "Apply now" button, you'll be leaving Fazow and going to an external job application page for this company.
Please research all companies before applying. When applying for jobs, you should NOT have to pay to apply.
Fazow accepts no liability or responsibility as a consequence of any reliance upon information on external sites or in jobs listed on fazow.com.
Job Description
Quality Assurance Technician
Location: Jacksonville, FL
As a Quality Assurance (QA) Technician, you will be responsible for assisting with quality-related activities including start-up verification, in-process verification & checks, BMR and documentation reviews, sampling, and inspection of finished products. Products include cannabis flower, cannabis oil, infused products (concentrates, capsules, lotions, tinctures, vapes, etc.) and food products (chocolate, gummies, lozenges, etc.). This position will also help ensure products are being produced in a manner that meets all specifications and brand consistency. You will also assist in identifying potential quality risks and working with operations personnel to develop improvement opportunities. The ideal candidate must possess a strong attention to detail and experience working within a highly regulated industry.
Job Summary and Responsibilities:
- Performs finished product sampling and inspection
- Performs equipment and product line clearances before production runs
- Performs in-process verification to ensure product weights, correct labeling & packaging
- Performs verification on finished products
- Inspects retain samples and customer return samples, as deemed necessary
- Assists in customer complaints and product investigations, helping to assess risk, identify root cause and quarantine product
- Inspects packaged orders to ensure correct content and quantities, as deemed necessary
- Reviews in-process batch documentation to ensure real-time compliance to product specifications, good documentation practices and written policies/procedures
- Monitors compliance to established Good Manufacturing Practice (GMP) and Safe Quality Foods guidance
- Conducts all duties in compliance with safety rules, applicable SOPs, and other applicable guidelines
- May require travel to other states or facilities to assist with inspections or quality issues
Required Experience, Education and Skills:
- Bachelors Degree, 1-3 years’ experience or Associate Degree, 5+ years’ experience
- Prior experience in highly regulated industry. Highly desirable: healthcare, medical devices, pharmaceutical, consumer packaged goods (food), cannabis. Highly desirable: FDA, HACCP, SQF experience
- Prior experience in Quality Assurance or Quality Control function
- Prior experience with product sampling, inspection procedures, customer complaints, product investigations, and CAPA
- Ability to follow written procedures and monitor others for adherence to written procedures
- Ability to create or update written procedures with site operations personnel
- Strong written and verbal communication skills
- Detail-oriented
- Utilizes critical thinking to troubleshoot issues, work collaboratively with a team to brainstorm solutions, and implement improvement solutions
- Must be flexible and able to work long hours and weekends as required
- Able to adapt in a quick and positive manner
- Able to work in a fast-paced environment and handle multiple tasks and requests
Additional Requirements:
- Must be 21 years of age or older
- Must comply with all legal and company regulations for working in the industry
- Ability to stand throughout extended periods, must be capable of squatting, standing, kneeling, bending, or walking throughout the workday
- Excellent communication skills and leadership both verbally and through written media.
- Strong decision-making, analytical and organizational skills
- Thorough understanding of state and local medical marijuana laws and how they apply to the operations
Physical Demands:
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.
While performing the duties of this Job, the employee is regularly required to stand for extended periods every day. The employee must regularly lift and /or move up to 25 pounds, frequently lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus. Able to work 6 days a week and evening shifts if required.
Work Environment:
While performing the duties of this job, the employee will be standing indoors and frequently exposed to laboratory conditions. The employee is frequently exposed to fumes or airborne particles; toxic or caustic chemicals; and varying temperatures. The noise level in the work environment is usually loud.
Job Type: Full-time
Job Type: Full-time
Pay: $15.00 - $18.00 per hour
Benefits:
- Dental insurance
- Employee discount
- Health insurance
- Paid time off
- Vision insurance
Schedule:
- 8 hour shift
- Monday to Friday
COVID-19 considerations:
All employees are required to wear a mask
Experience:
- Quality control: 1 year (Required)
Work Location: One location
Apply for this job with VidaCann
Apply now →
By clicking the "Apply now" button, you'll be leaving Fazow and going to an external job application page for this company.
Please research all companies before applying. When applying for jobs, you should NOT have to pay to apply.
Fazow accepts no liability or responsibility as a consequence of any reliance upon information on external sites or in jobs listed on fazow.com.
THE TEAM:
Founded in 2018 and headquartered in Boca Raton, Florida, Jushi is a vertically integrated, multi-state cannabis company that develops and operates high-end retail locations, premium brands, state-of-the-art cultivation, processing, manufacturing facilities, along with a cutting-edge online platform that is setting a new standard for a sophisticated, data-driven, modern cannabis experience.
Since its founding in 2018, Jushi has grown from just a handful of people with an idea to more than 900 employees strong. The Company has scaled its operations in seven states, including Pennsylvania, Virginia, Massachusetts, Illinois, California, Nevada, and Ohio, and has been named one of the top five cannabis companies to work for by Cannabis Business Times.
The Company operates more than two dozen retail locations across the country under the retail brand, BEYOND / HELLO™ as well as under the recently acquired brand, Nature’s Remedy. The Company provides an unparalleled in-store experience, coupled with online reservations and in-store express pickup.
Each day, Jushi team members continue to grow, cultivate, process and manufacture a comprehensive suite of cannabis brands under the names: The Bank, The Lab, Tasteology, Nira + Medicinals and Sèche, which are addressing a wide variety of consumer and patient needs across multiple states
THE OPPORTUNITY
Want to make a meaningful difference in peoples’ lives while earning a competitive salary? At Jushi, we are shaping the future of the cannabis industry, the fastest growing jobs sector in the U.S. The Quality Assurance (QA) Technician will be responsible for assisting in all quality aspects of the production site and ensure all products are manufactured in compliance with 21CFR111 requirements. The QA Technician is responsible for quality inspections of Medical Cannabis products and auditing the processes and procedures in the medical cannabis manufacturing operation. They are required to follow set processes and ensure adherence to state regulations, SOPs, work instructions (WI), and adhere to good manufacturing practices (GMP), good laboratory practices (GLP) and other product quality standards.
WHAT YOU WILL DO
- Perform Quality Inspections on products, equipment, and procedures.
- Responsible for monitoring cannabis product quality and safety throughout the manufacturing process.
- Responsible for performing verification of sanitation, equipment and other areas as required.
- Responsible for auditing the correct recording and filing of all relevant record logs and documentation completed by staff.
- Ensures the correct guidelines for production are followed during operations.
- Ensures employees are following all SOP’s, Work Instructions, and worker safety practices.
- Assist Quality Manager with instructing employees on Quality Improvements or Issues.
- Collect product samples for Product Development, lab retains and the laboratory when directed.
- May perform or assist inventory management personnel with inventory audits when needed.
- Support team members on quality management program to ensure there is an in-depth understanding of program and individual responsibilities.
- Provide support to GMP production operations, including conducting SOPs, training, and serve as resource to operations for quality controls and GMP compliance.
- Support improvement and alignment of the Quality Management Systems at site level.
- Conduct all duties in compliance with safety rules, applicable SOPs, and other relevant guidelines.
- Support all staff in data collection and analysis, reporting activities that support quality improvement interventions, transparency, compliance regulatory standards and provide performance monitoring.
- Support review and approval of batch record documentation, including validation protocols, master batch records, analytical test results, packaging, and labeling documentation.
EDUCATION & EXPERIENCE
- Familiarity with FDA regulations and/or operating in a regulated environment preferred.
- Attention to detail and ability to record numerical data and understand nomenclature and lot/Batch numbering systems.
- Ability to be flexible and provide support to any department within the organization as required by Operations leadership.
- Must be able to read and write in English and the ability to perform basic calculations.
- Microsoft Office skills.
- Must pass criminal background check.
PHYSICAL REQUIRMENTS
- Regularly perform desk-based computer tasks
- Frequently sitting and standing
- Occasionally Twist/bend/stoop/squat, kneel/crawl
- An environment with minimal noise levels
OTHER DUTIES
Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice
Jushi is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity or expression, religion, national origin or ancestry, age, disability, marital status, pregnancy, protected veteran status, protected genetic information, political affiliation, or any other characteristics protected by local laws, regulations, or ordinances.
We offer benefit packages that may include: Medical, Dental, Vision, Life, Short, and Long Term Disability, Flexible Spending Accounts, Paid Time Off, and Paid Holidays.
Job Type: Full-time
Schedule:
- 8 hour shift
Ability to commute/relocate:
- Lakeville, MA: Reliably commute or planning to relocate before starting work (Required)
Experience:
- Manufacturing: 1 year (Preferred)
Work Location: One location
Apply for this job with Jushi
Apply now →
By clicking the "Apply now" button, you'll be leaving Fazow and going to an external job application page for this company.
Please research all companies before applying. When applying for jobs, you should NOT have to pay to apply.
Fazow accepts no liability or responsibility as a consequence of any reliance upon information on external sites or in jobs listed on fazow.com.
As a Quality Assurance (QA) Technician, you will be responsible for assisting with quality-related activities including start-up verification, in-process verification & checks, BMR and documentation reviews, sampling, and inspection of finished products. Products include cannabis flower, cannabis oil, infused products (concentrates, capsules, lotions, tinctures, vapes, etc.) and food products (chocolate, gummies, lozenges, etc.). This position will also help ensure products are being produced in a manner that meets all specifications and brand consistency. You will also assist in identifying potential quality risks and working with operations personnel to develop improvement opportunities. The ideal candidate must possess a strong attention to detail and experience working within a highly regulated industry.
Job Summary and Responsibilities:
- Performs finished product sampling and inspection
- Performs equipment and product line clearances before production runs
- Performs in-process verification to ensure product weights, correct labeling & packaging
- Performs verification on finished products
- Inspects retain samples and customer return samples, as deemed necessary
- Assists in customer complaints and product investigations, helping to assess risk, identify root cause and quarantine product
- Inspects packaged orders to ensure correct content and quantities, as deemed necessary
- Reviews in-process batch documentation to ensure real-time compliance to product specifications, good documentation practices and written policies/procedures
- Monitors compliance to established Good Manufacturing Practice (GMP) and Safe Quality Foods guidance
- Conducts all duties in compliance with safety rules, applicable SOPs, and other applicable guidelines
- May require travel to other states or facilities to assist with inspections or quality issues
Required Experience, Education and Skills:
- Bachelors Degree, 1-3 years’ experience or Associate Degree, 5+ years’ experience
- Prior experience in highly regulated industry. Highly desirable: healthcare, medical devices, pharmaceutical, consumer packaged goods (food), cannabis. Highly desirable: FDA, HACCP, SQF experience
- Prior experience in Quality Assurance or Quality Control function
- Prior experience with product sampling, inspection procedures, customer complaints, product investigations, and CAPA
- Ability to follow written procedures and monitor others for adherence to written procedures
- Ability to create or update written procedures with site operations personnel
- Strong written and verbal communication skills
- Detail-oriented
- Utilizes critical thinking to troubleshoot issues, work collaboratively with a team to brainstorm solutions, and implement improvement solutions
- Must be flexible and able to work long hours and weekends as required
- Able to adapt in a quick and positive manner
- Able to work in a fast-paced environment and handle multiple tasks and requests
Additional Requirements:
- Must be 21 years of age or older
- Must comply with all legal and company regulations for working in the industry
- Ability to stand throughout extended periods, must be capable of squatting, standing, kneeling, bending, or walking throughout the workday
- Excellent communication skills and leadership both verbally and through written media.
- Strong decision-making, analytical and organizational skills
- Thorough understanding of state and local medical marijuana laws and how they apply to the operations
- COVID-19 considerations: For the safety of you and the team, we require proof of COVID-19 vaccination before hire.
Physical Demands:
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.
While performing the duties of this Job, the employee is regularly required to stand for extended periods every day. The employee must regularly lift and /or move up to 25 pounds, frequently lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus. Able to work 6 days a week and evening shifts if required.
Work Environment:
While performing the duties of this job, the employee will be standing indoors and frequently exposed to laboratory conditions. The employee is frequently exposed to fumes or airborne particles; toxic or caustic chemicals; and varying temperatures. The noise level in the work environment is usually loud.
Job Type: Full-time
Pay: From $15.00 per hour
Benefits:
- 401(k)
- Dental insurance
- Employee discount
- Health insurance
- Paid time off
- Vision insurance
Schedule:
- 10 hour shift
- 12 hour shift
- 8 hour shift
- Day shift
- Night shift
- Overtime
- Weekend availability
Ability to commute/relocate:
- Jacksonville, FL 32216: Reliably commute or planning to relocate before starting work (Required)
Experience:
- Manufacturing: 1 year (Preferred)
Shift availability:
- Day Shift (Preferred)
- Night Shift (Preferred)
Work Location: One location
Apply for this job with VidaCann
Apply now →
By clicking the "Apply now" button, you'll be leaving Fazow and going to an external job application page for this company.
Please research all companies before applying. When applying for jobs, you should NOT have to pay to apply.
Fazow accepts no liability or responsibility as a consequence of any reliance upon information on external sites or in jobs listed on fazow.com.
THE TEAM:
Founded in 2018 and headquartered in Boca Raton, Florida, Jushi is a vertically integrated, multi-state cannabis company that develops and operates high-end retail locations, premium brands, state-of-the-art cultivation, processing, manufacturing facilities, along with a cutting-edge online platform that is setting a new standard for a sophisticated, data-driven, modern cannabis experience.
Since its founding in 2018, Jushi has grown from just a handful of people with an idea to more than 900 employees strong. The Company has scaled its operations in seven states, including Pennsylvania, Virginia, Massachusetts, Illinois, California, Nevada, and Ohio, and has been named one of the top five cannabis companies to work for by Cannabis Business Times.
The Company operates more than two dozen retail locations across the country under the retail brand, BEYOND / HELLO™ as well as under the recently acquired brand, Nature’s Remedy. The Company provides an unparalleled in-store experience, coupled with online reservations and in-store express pickup.
Each day, Jushi team members continue to grow, cultivate, process and manufacture a comprehensive suite of cannabis brands under the names: The Bank, The Lab, Tasteology, Nira + Medicinals and Sèche, which are addressing a wide variety of consumer and patient needs across multiple states
THE OPPORTUNITY
Want to make a meaningful difference in peoples’ lives while earning a competitive salary? At Jushi, we are shaping the future of the cannabis industry, the fastest growing jobs sector in the U.S. The Quality Assurance (QA) Technician will be responsible for assisting in all quality aspects of the production site and ensure all products are manufactured in compliance with 21CFR111 requirements. The QA Technician is responsible for quality inspections of Medical Cannabis products and auditing the processes and procedures in the medical cannabis manufacturing operation. They are required to follow set processes and ensure adherence to state regulations, SOPs, work instructions (WI), and adhere to good manufacturing practices (GMP), good laboratory practices (GLP) and other product quality standards.
WHAT YOU WILL DO
Perform Quality Inspections on products, equipment, and procedures.- Responsible for monitoring cannabis product quality and safety throughout the manufacturing process.
- Responsible for performing verification of sanitation, equipment and other areas as required.
- Responsible for auditing the correct recording and filing of all relevant record logs and documentation completed by staff.
- Ensures the correct guidelines for production are followed during operations.
- Ensures employees are following all SOP’s, Work Instructions, and worker safety practices.
- Assist Quality Manager with instructing employees on Quality Improvements or Issues.
- Collect product samples for Product Development, lab retains and the laboratory when directed.
- May perform or assist inventory management personnel with inventory audits when needed.
- Support team members on quality management program to ensure there is an in-depth understanding of program and individual responsibilities.
- Provide support to GMP production operations, including conducting SOPs, training, and serve as resource to operations for quality controls and GMP compliance.
- Support improvement and alignment of the Quality Management Systems at site level.
- Conduct all duties in compliance with safety rules, applicable SOPs, and other relevant guidelines.
- Support all staff in data collection and analysis, reporting activities that support quality improvement interventions, transparency, compliance regulatory standards and provide performance monitoring.
- Support review and approval of batch record documentation, including validation protocols, master batch records, analytical test results, packaging, and labeling documentation.
EDUCATION & EXPERIENCE
Familiarity with FDA regulations and/or operating in a regulated environment preferred.- Attention to detail and ability to record numerical data and understand nomenclature and lot/Batch numbering systems.
- Ability to be flexible and provide support to any department within the organization as required by Operations leadership.
- Must be able to read and write in English and the ability to perform basic calculations.
- Microsoft Office skills.
- Must pass criminal background check.
PHYSICAL REQUIRMENTS
Regularly perform desk-based computer tasks- Frequently sitting and standing
- Occasionally Twist/bend/stoop/squat, kneel/crawl
- An environment with minimal noise levels
OTHER DUTIES
Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice
Jushi is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity or expression, religion, national origin or ancestry, age, disability, marital status, pregnancy, protected veteran status, protected genetic information, political affiliation, or any other characteristics protected by local laws, regulations, or ordinances.
We offer benefit packages that may include: Medical, Dental, Vision, Life, Short, and Long Term Disability, Flexible Spending Accounts, Paid Time Off, and Paid Holidays.
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Apply for this job with Jushi
Apply now →
By clicking the "Apply now" button, you'll be leaving Fazow and going to an external job application page for this company.
Please research all companies before applying. When applying for jobs, you should NOT have to pay to apply.
Fazow accepts no liability or responsibility as a consequence of any reliance upon information on external sites or in jobs listed on fazow.com.
“Trulieve Grows One Patient at a Time”
If you have an interest in being part of one of the fastest growing industries in the nation in you may consider wanting to work for Trulieve! If you have a desire to help others in need through your efforts, this may be the role for you!
At Trulieve, we strive to bring our patients the relief they need in a product they can trust. Our plants are hand-grown in an environment specially designed to reduce unwanted chemicals and pests, keeping the process as natural as possible at every turn.
Our products are designed to alleviate seizures, severe and persistent muscle spasms, pain, nausea, loss of appetite, and other symptoms associated with serious medical conditions such as cancer.
Our specially trained staff works hand-in-hand with physicians to provide the right products and the correct dosage to ensure patients get the compassionate care they need.
Requisition ID: 2310
Remote Work Available: No
Job Summary
The Quality Assurance Technician is responsible for conducting visual scans on products in effort to assure quality and safety of products intended for consumers. QA Techs will be responsible for tracking the weight of each sample and keeping track of what cultivar is currently being worked on. Additionally, QA Techs will be required to safely handle and separate any adulterated product that is found during scans.
Key Responsibilities
- Conduct visual inspections of cannabis for organic and inorganic adulterants and defects
- Document inspection results by completing reports and logs and inputting data into quality database
- Keep equipment (i.e. scales, tools, etc) in good, working order
- Maintain a safe and healthy work environment by following departmental standard operating procedures (SOPs), adhering to cGMP SOPs, and complying with legal regulations
- Maintains and ensures that proper PPE is utilized and changed out regularly, or as needed
- Provide feedback as needed
- Performs other duties as required
Education and Experience
- High School Diploma or GED
- Detail oriented
- Coachable and a willingness to learn
- Ability to work in a fast-paced environment
- Ability to focus and avoid distractions
- Comfortable operating digital scales
- Basic computer knowledge
- Basic math and reading comprehension
- Organizational skills
Additional Requirements
- Must be at least 21 years of age (or 18 years of age in CT, PA and WV).
- Driver's License or ability to obtain one.
- Must be and remain compliant with any and all legal or company regulations for working in the cannabis industry.
- Must successfully complete a comprehensive background check.
Physical Requirements
- Must be able to push, pull, move, and/or lift a minimum of 50lbs to a minimum height of 5 feet and able to push, pull, move, and/or carry such weight a minimum distance of 50 feet, with or without mechanical assistance.
- Must be able to work seated/standing as appropriate at workstations for extended periods of time, maintain body equilibrium while climbing ladders, stairways, stooping, kneeling, crouching, and reaching, and use hands/fingers to hold, grasp, turn, pick, pinch frequently/constantly to complete tasks.
- Must be able to handle organic matter daily, able to wear PPE as appropriate (eye, face, hand, arm, head, foot, body, fall protection), and able to be exposed to hot, cold, wet, humid, or windy conditions while wearing PPE (95 degrees or greater).
- Must have visual acuity with/without job aids to perform activities such as; reading, viewing a computer terminal, visual inspection involving small parts/details. Clarity of vision at 20 ft or more in day and night/dark conditions
- Must be able to speak and communicate verbally at conversation levels with co-workers, vendors, etc. (Moderate noise).
Salary will be commensurate with experience. A comprehensive benefits package including paid time off is offered with this position. This position will work an average of 40 hours per week and will be available “after hours” if an emergency situation should arise.
Trulieve provides equal employment opportunities to all employees and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, pregnancy or any other characteristic protected by federal, state or local laws.
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“Trulieve Grows One Patient at a Time”
If you have an interest in being part of one of the fastest growing industries in the nation in you may consider wanting to work for Trulieve! If you have a desire to help others in need through your efforts, this may be the role for you!
At Trulieve, we strive to bring our patients the relief they need in a product they can trust. Our plants are hand-grown in an environment specially designed to reduce unwanted chemicals and pests, keeping the process as natural as possible at every turn.
Our products are designed to alleviate seizures, severe and persistent muscle spasms, pain, nausea, loss of appetite, and other symptoms associated with serious medical conditions such as cancer.
Our specially trained staff works hand-in-hand with physicians to provide the right products and the correct dosage to ensure patients get the compassionate care they need.
Requisition ID: 2208
Remote Work Available: No
Job Title: Quality Assurance Technician
FLSA Status: Regular Full-Time
Salary: Hourly
Location: Lesage, West Virginia|
Key Duties and Responsibilities:
- Report to the Quality Assurance Manager/Quality Assurance Department for daily assignments and coordination for daily tasks to meet and exceed quality assurance deadlines.
- Assisting in the drafting, editing of technical documents such as work instructions and SOPs.
- Assisting in organizing and maintaining doc control systems and hard copy paperwork in association with cGMP standards/guidelines.
- Monitoring employee activities as needed to file non-conformance reports when necessary.
- You will be responsible for the inspection of processes in propagation, cultivation, trimming, extraction, and packaging & labeling. You will also be assigned to technical projects as needed to inspect final products, assist with third party lab sampling, inventory compliance, general compliance, internal audits of facilities sanitation, pest control and other projects that are deemed necessary to quality assurance within the facility.
Requirements
SKILLS AND QUALIFICATIONS:
- HACCP certification preferred but not necessary
- Knowledge of cGMP/CFR 21
- Must possess excellent communication skills for liaising and communicating with vendors, customers, and internal departments.
- Practical experience with risk management, product testing, capability studies, and control plans.
- Highly motivated and self-directed capable of multi-tasking, and able to work with minimal supervision.
- Strong leadership abilities and the capability of motivating a diverse team.
- Able to interface directly with cross-functional teams.
- Extremely detail-oriented and analytical thinker.
- Ability to create and review technical documentation, including project plans, test procedures, and design documents.
- Able to develop, review, and maintain metrics and quality audits.
- Strong problem identification and problem resolution skills.
- A well-defined sense of diplomacy, including solid negotiation, conflict resolution, and people management skills.
- Strong work ethic and positive team attitude.
- Well-developed problem-solving skills and ability to develop conceptual alternatives.
- Able to find new methods and principles and ability to incorporate them into existing practices as needed.
- High degree of resourcefulness, flexibility, and adaptability.
- Must have the ability to plan, organize, develop, implement and interpret the programs, goals, objectives, policies, procedures, etc.
- Strong negotiation and prioritization skills.
- Experience with MS Office (Excel, Word, Outlook, and Access) and be able to handle working with multiple programs.
- Ability to read/write English at a proficient level.
ADDITIONAL REQUIREMENTS:
- Per state law, must be a minimum of 21 years of age.
- Must be and remain compliant with any and all legal or company regulations for working in the cannabis industry.
- Must successfully complete a comprehensive background check.
PHYSICAL REQUIREMENTS:
- Must be able to push, pull, move, and/or lift a minimum of 40lbs to a minimum height of 5 feet and able to push, pull, move, and/or carry such weight a minimum distance of 50 feet, with or without mechanical assistance
- Must be able to work seated/standing as appropriate at workstations for extended periods of time, maintain body equilibrium while climbing ladders, stairways, stopping, kneeling, crouching, and reaching, and use hands/fingers to hold, grasp, turn, pick, pinch frequently/constantly to complete tasks
- Must be able to handle organic matter daily, able to wear PPE as appropriate (eye, face, hand, arm, head, foot, body, fall protection), and able to be exposed to hot, cold, wet, humid, or windy conditions while wearing PPE (95 degrees or greater)
- Must have visual acuity with/without job aids to perform activities such as; reading, viewing a computer terminal, visual inspection involving small parts/details. Clarity of vision at 20 ft or more in day and night/dark conditions
- Must be able to speak and communicate verbally at conversation levels with co-workers, vendors, etc. (Moderate noise)
WORK SCHEDULE:
- 40+ hours weekly with flexible hours depending on department needs. Must be available to work occasional evenings, weekends, and holidays
Equal Opportunity Employer l Trulieve Supports a Drug Free Workplace
Salary will be commensurate with experience. A comprehensive benefits package including paid time off is offered with this position. This position will work an average of 40 hours per week and will be available “after hours” if an emergency situation should arise.
Trulieve provides equal employment opportunities to all employees and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, pregnancy or any other characteristic protected by federal, state or local laws.
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THE TEAM:
Founded in 2018 and headquartered in Boca Raton, Florida, Jushi is a vertically integrated, multi-state cannabis company that develops and operates high-end retail locations, premium brands, state-of-the-art cultivation, processing, manufacturing facilities, along with a cutting-edge online platform that is setting a new standard for a sophisticated, data-driven, modern cannabis experience.
Since its founding in 2018, Jushi has grown from just a handful of people with an idea to more than 900 employees strong. The Company has scaled its operations in seven states, including Pennsylvania, Virginia, Massachusetts, Illinois, California, Nevada, and Ohio, and has been named one of the top five cannabis companies to work for by Cannabis Business Times.
The Company operates more than two dozen retail locations across the country under the retail brand, BEYOND / HELLO™ as well as under the recently acquired brand, Nature’s Remedy. The Company provides an unparalleled in-store experience, coupled with online reservations and in-store express pickup.
Each day, Jushi team members continue to grow, cultivate, process and manufacture a comprehensive suite of cannabis brands under the names: The Bank, The Lab, Tasteology, Nira + Medicinals and Sèche, which are addressing a wide variety of consumer and patient needs across multiple states
THE OPPORTUNITY
Want to make a meaningful difference in peoples’ lives while earning a competitive salary? At Jushi, we are shaping the future of the cannabis industry, the fastest growing jobs sector in the U.S. The Quality Assurance (QA) Technician will be responsible for assisting in all quality aspects of the production site and ensure all products are manufactured in compliance with 21CFR111 requirements. The QA Technician is responsible for quality inspections of Medical Cannabis products and auditing the processes and procedures in the medical cannabis manufacturing operation. They are required to follow set processes and ensure adherence to state regulations, SOPs, work instructions (WI), and adhere to good manufacturing practices (GMP), good laboratory practices (GLP) and other product quality standards.
WHAT YOU WILL DO
- Perform Quality Inspections on products, equipment, and procedures.
- Responsible for monitoring cannabis product quality and safety throughout the manufacturing process.
- Responsible for performing verification of sanitation, equipment and other areas as required.
- Responsible for auditing the correct recording and filing of all relevant record logs and documentation completed by staff.
- Ensures the correct guidelines for production are followed during operations.
- Ensures employees are following all SOP’s, Work Instructions, and worker safety practices.
- Assist Quality Manager with instructing employees on Quality Improvements or Issues.
- Collect product samples for Product Development, lab retains and the laboratory when directed.
- May perform or assist inventory management personnel with inventory audits when needed.
- Support team members on quality management program to ensure there is an in-depth understanding of program and individual responsibilities.
- Provide support to GMP production operations, including conducting SOPs, training, and serve as resource to operations for quality controls and GMP compliance.
- Support improvement and alignment of the Quality Management Systems at site level.
- Conduct all duties in compliance with safety rules, applicable SOPs, and other relevant guidelines.
- Support all staff in data collection and analysis, reporting activities that support quality improvement interventions, transparency, compliance regulatory standards and provide performance monitoring.
- Support review and approval of batch record documentation, including validation protocols, master batch records, analytical test results, packaging, and labeling documentation.
EDUCATION & EXPERIENCE
- Familiarity with FDA regulations and/or operating in a regulated environment preferred.
- Attention to detail and ability to record numerical data and understand nomenclature and lot/Batch numbering systems.
- Ability to be flexible and provide support to any department within the organization as required by Operations leadership.
- Must be able to read and write in English and the ability to perform basic calculations.
- Microsoft Office skills.
- Must pass criminal background check.
PHYSICAL REQUIRMENTS
- Regularly perform desk-based computer tasks
- Frequently sitting and standing
- Occasionally Twist/bend/stoop/squat, kneel/crawl
- An environment with minimal noise levels
OTHER DUTIES
Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice
Jushi is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity or expression, religion, national origin or ancestry, age, disability, marital status, pregnancy, protected veteran status, protected genetic information, political affiliation, or any other characteristics protected by local laws, regulations, or ordinances.
We offer benefit packages that may include: Medical, Dental, Vision, Life, Short, and Long Term Disability, Flexible Spending Accounts, Paid Time Off, and Paid Holidays.
Job Type: Full-time
Schedule:
- 8 hour shift
Ability to commute/relocate:
- Lakeville, MA: Reliably commute or planning to relocate before starting work (Required)
Experience:
- Manufacturing: 1 year (Preferred)
Work Location: One location
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As a Quality Assurance (QA) Technician, you will be responsible for assisting with quality-related activities including start-up verification, in-process verification & checks, BMR and documentation reviews, sampling, and inspection of finished products. Products include cannabis flower, cannabis oil, infused products (concentrates, capsules, lotions, tinctures, vapes, etc.) and food products (chocolate, gummies, lozenges, etc.). This position will also help ensure products are being produced in a manner that meets all specifications and brand consistency. You will also assist in identifying potential quality risks and working with operations personnel to develop improvement opportunities. The ideal candidate must possess a strong attention to detail and experience working within a highly regulated industry.
Job Summary and Responsibilities:
- Performs finished product sampling and inspection
- Performs equipment and product line clearances before production runs
- Performs in-process verification to ensure product weights, correct labeling & packaging
- Performs verification on finished products
- Inspects retain samples and customer return samples, as deemed necessary
- Assists in customer complaints and product investigations, helping to assess risk, identify root cause and quarantine product
- Inspects packaged orders to ensure correct content and quantities, as deemed necessary
- Reviews in-process batch documentation to ensure real-time compliance to product specifications, good documentation practices and written policies/procedures
- Monitors compliance to established Good Manufacturing Practice (GMP) and Safe Quality Foods guidance
- Conducts all duties in compliance with safety rules, applicable SOPs, and other applicable guidelines
- May require travel to other states or facilities to assist with inspections or quality issues
Required Experience, Education and Skills:
- Bachelors Degree, 1-3 years’ experience or Associate Degree, 5+ years’ experience
- Prior experience in highly regulated industry. Highly desirable: healthcare, medical devices, pharmaceutical, consumer packaged goods (food), cannabis. Highly desirable: FDA, HACCP, SQF experience
- Prior experience in Quality Assurance or Quality Control function
- Prior experience with product sampling, inspection procedures, customer complaints, product investigations, and CAPA
- Ability to follow written procedures and monitor others for adherence to written procedures
- Ability to create or update written procedures with site operations personnel
- Strong written and verbal communication skills
- Detail-oriented
- Utilizes critical thinking to troubleshoot issues, work collaboratively with a team to brainstorm solutions, and implement improvement solutions
- Must be flexible and able to work long hours and weekends as required
- Able to adapt in a quick and positive manner
- Able to work in a fast-paced environment and handle multiple tasks and requests
Additional Requirements:
- Must be 21 years of age or older
- Must comply with all legal and company regulations for working in the industry
- Ability to stand throughout extended periods, must be capable of squatting, standing, kneeling, bending, or walking throughout the workday
- Excellent communication skills and leadership both verbally and through written media.
- Strong decision-making, analytical and organizational skills
- Thorough understanding of state and local medical marijuana laws and how they apply to the operations
- COVID-19 considerations: For the safety of you and the team, we require proof of COVID-19 vaccination before hire.
Physical Demands:
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.
While performing the duties of this Job, the employee is regularly required to stand for extended periods every day. The employee must regularly lift and /or move up to 25 pounds, frequently lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus. Able to work 6 days a week and evening shifts if required.
Work Environment:
While performing the duties of this job, the employee will be standing indoors and frequently exposed to laboratory conditions. The employee is frequently exposed to fumes or airborne particles; toxic or caustic chemicals; and varying temperatures. The noise level in the work environment is usually loud.
Job Type: Full-time
Benefits:
- Dental insurance
- Employee discount
- Health insurance
- Paid time off
- Vision insurance
Schedule:
- 10 hour shift
- 12 hour shift
- 8 hour shift
- Day shift
- Night shift
- Overtime
- Weekend availability
Ability to commute/relocate:
- Jacksonville, FL 32216: Reliably commute or planning to relocate before starting work (Required)
Experience:
- Manufacturing: 1 year (Preferred)
Shift availability:
- Day Shift (Preferred)
- Night Shift (Preferred)
Work Location: One location
Apply for this job with VidaCann
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DFMMJ Investments, LLC, d/b/a Liberty Health Sciences Florida, Ltd. is a Medical Marijuana Treatment Center that has been granted a license by the Florida Department of Health to cultivate, process, transport, and dispense low-THC cannabis, medical cannabis, and cannabis delivery devices pursuant to Florida Statutes.
JOB SUMMARY:
The QA/QC Technician will work under direction of the Quality Manager to develop, implement, manage, and continually improve the Liberty Heath Sciences quality and product safety programs.
CORE RESPONSIBILITIES:
- Inspects in-process and/or finished products for conformance to quality assurance standards
- Assist in monthly GMP/Sanitation/Security inspections and follow up on corrective actions
- Perform Pre-operational checks including sanitation swabbing
- Perform quality checks on incoming materials
- Sampling of raw materials
- Assist with document control and change management as necessary
- Assist in investigating consumer complaints by determining root cause, implementing corrective actions and preventive measures, responding to complaints in the required time-frame, and analyzing complaint trends.
- Initiate and conduct Corrective Action Preventive Action (CAPA) investigations.
- Maintain records for GMP training, including QPs, SOPs etc.
- Ensure all employees are trained on the procedures for their departments
- Follow all Good Manufacturing Practices as outlined in the QA Manual
- Perform other duties as needed and requested by the Quality Manager such as batch record and COA reviews as needed.
Requirements
DESIRED SKILLS & EXPERIENCE:
- Must be able to work independently and as a team
- Quality related experience in food, horticulture, pharmaceutical or other related field preferred
- Basic computer skills (Microsoft Word, Outlook, etc.)
- Must be over 21 years or older
- Must be able to pass a Level II Background Check
- Work authorization United States (Required)
Physical Demands
- Must be able to stand for extended periods of time, and safely lift up to 25lbs
- Must be able to wear required Personal Protective Equipment (PPE) for extended periods of time (i.e. gloves, lab coat, hair net)
- Appropriate grooming for work environment (no jewelry, hair must be tied back, no hair outside of PPE)
Position Type/Expected Hours of Work
This is a full-time position, open availability 40 hours.
Required Education and Experience
Laboratory, Analytical Testing
High School Diploma
Science Degree Preferred
Benefits
Medical benefits, dental and vision on the first of the month after 60 days of employment.
Liberty Health Sciences, LLC, provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability, genetics or veteran status. In addition to federal law requirements, Liberty Health Sciences, LLC complies with applicable state and local laws governing non-discrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.
Liberty health Sciences, LLC expressly prohibits any form of workplace harassment based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, genetic information, disability, or veteran status. Improper interference with the ability of Liberty Health Sciences, LLC’s employees to perform their job duties may result in discipline up to and including discharge.
Apply for this job with Liberty Health Sciences
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Fazow accepts no liability or responsibility as a consequence of any reliance upon information on external sites or in jobs listed on fazow.com.
DFMMJ Investments, LLC, d/b/a Liberty Health Sciences Florida, Ltd. is a Medical Marijuana Treatment Center that has been granted a license by the Florida Department of Health to cultivate, process, transport, and dispense low-THC cannabis, medical cannabis, and cannabis delivery devices pursuant to Florida Statutes.
JOB SUMMARY:
The QA/QC Technician will work under direction of the Quality Manager to develop, implement, manage, and continually improve the Liberty Heath Sciences quality and product safety programs.
CORE RESPONSIBILITIES:
- Inspects in-process and/or finished products for conformance to quality assurance standards
- Assist in monthly GMP/Sanitation/Security inspections and follow up on corrective actions
- Perform Pre-operational checks including sanitation swabbing
- Perform quality checks on incoming materials
- Sampling of raw materials
- Assist with document control and change management as necessary
- Assist in investigating consumer complaints by determining root cause, implementing corrective actions and preventive measures, responding to complaints in the required time-frame, and analyzing complaint trends.
- Initiate and conduct Corrective Action Preventive Action (CAPA) investigations.
- Maintain records for GMP training, including QPs, SOPs etc.
- Ensure all employees are trained on the procedures for their departments
- Follow all Good Manufacturing Practices as outlined in the QA Manual
- Perform other duties as needed and requested by the Quality Manager such as batch record and COA reviews as needed.
Requirements
DESIRED SKILLS & EXPERIENCE:
- Must be able to work independently and as a team
- Quality related experience in food, horticulture, pharmaceutical or other related field preferred
- Basic computer skills (Microsoft Word, Outlook, etc.)
- Must be over 21 years or older
- Must be able to pass a Level II Background Check
- Work authorization United States (Required)
Physical Demands
- Must be able to stand for extended periods of time, and safely lift up to 25lbs
- Must be able to wear required Personal Protective Equipment (PPE) for extended periods of time (i.e. gloves, lab coat, hair net)
- Appropriate grooming for work environment (no jewelry, hair must be tied back, no hair outside of PPE)
Position Type/Expected Hours of Work
This is a full-time position, open availability 40 hours.
Required Education and Experience
Laboratory, Analytical Testing
High School Diploma
Science Degree Preferred
Benefits
Medical benefits, dental and vision on the first of the month after 60 days of employment.
Liberty Health Sciences, LLC, provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability, genetics or veteran status. In addition to federal law requirements, Liberty Health Sciences, LLC complies with applicable state and local laws governing non-discrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.
Liberty health Sciences, LLC expressly prohibits any form of workplace harassment based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, genetic information, disability, or veteran status. Improper interference with the ability of Liberty Health Sciences, LLC’s employees to perform their job duties may result in discipline up to and including discharge.
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Position Description
This position is responsible for supervising and implementation of Food Safety, Work Safety, Compliance and Quality Assurance programs designed to meet State and Federal (cGMP) regulations for the cultivation, processing, and production of cannabis and cannabis-infused products.
The ideal candidate will have direct experience as a quality and/or compliance leader in the Cannabis industry, or a similar highly regulated industry such as food and beverage. A demonstrated track record implementing and maintaining a robust operational compliance program for Consumer-Packaged Goods ("CPG") facilities—including developing SOPs and leading internal audits—is preferred. A practical experience in cGMP, HACCP, ISO and SQF Management System Standards will be most desired. The candidates must be a PCQI or be willing to achieve certification in the shortest possible time.
This position will report to the Quality Assurance Manager/Director at MariMed Corporate for technical and systems activities.
This position will report to the Facility General Manager on operational and facility specific compliance related activities.
Duties and Responsibilities
- Collaborate with relevant persons to Design, Develop, Implement and Maintain quality and safety management system to include SOPs, forms, and regulated documents for approval and implementation.
- Develop, implement, and monitor policies and procedures for food safety following state code, HACCP, Review, write and edit SOPs with a focus on achieving cGMP and other Management Systems (Food Safety, Work Safety) conformance and compliance 21 CFR 111 and 21 CFR 117, OSHA as well as state specific work safety as required.
- Monitor training and quality and safety performance at the facility.
- Report to facility leadership – KPIs, initiatives, issues, corrective action, and customer complaints.
- Provide guidance and lead problem solving and corrective actions involving food safety and quality issues at the facility.
- Interpret quality and safety philosophy to key personnel in the facility and potential business impact.
- Authority to accept/reject products, in-process components, raw materials, packaging, labels and more based on quality and safety.
- Train and lead in all work safety, food safety and product quality related activities.
- Manage Contracts in collaborations with other stakeholders and Supplier Evaluation Program specific to the facility.
- Manage food safety and quality audit programs (internal and external)
- Lead the configuration, implementation, and management of Document Management Software at the facility.
- Recommend and/or develop orientation and training programs for quality, safety, food safety, GMP training. Assist members of the facility team in training as appropriate
- Works closely with third party testing labs to improve success rate of potency and contaminant testing for product certificate of analyses.
- Serve as primary facility liaison to third party GMP consultants and certifying organizations. This includes participating in and leading meetings to keep team “on track” and ensure timelines are met.
- Communicate to all relevant personnel all information essential to ensure the effective implementation and maintenance of GMP systems.
- Develop internal audit systems focused on quality and compliance. Ensure follow-up to identified issues.
- Serve as primary liaison with ITL (independent testing labs). Maintain, organize, and review test results to support ongoing quality assurance.
- Assist Cannabis Inventory Manager on facility audits and compilation and review of METRC and Leaflogix data related to the cultivation, production, and processing operations.
- Ensures that the facility meets the company’s, industries and regulatory standards for food safety and product integrity always.
- Oversees complaint investigations and ensures corrective action is being reported and followed up on
- Ensures that the unit is up to standards for audits, pest control, working with Facility Managers on Sanitation.
- Works closely with the vendor(s)/Supply Chain to ensure that approved chemicals are in use for processes and sanitation.
- Monitors training and development and provides coaching, direction, and leadership support to staff in the form of new hire orientation, retraining, annual refresher training.
- Perform specific tasks as may be assigned by Facility Quality Assurance Manager.
Education and Professional Requirements:
§ 2+ years of experience as a quality and safety assurance technician/manager in Dietary/Natural Products, Food or Pharmaceutical industry.
§ BS or BA degree in food science, food engineering, microbiology, chemistry, or other similar science related field.
§ HACCP & PCQI certified preferred
§ Computer Skills: MS Office applications, GMP software
§ Excellent oral and written skills; ability to tailor to audience.
§ Ability to interface with multiple groups – from front line operators to General Manager and customers.
Physical Requirements and Working Conditions:
§ Ability to lift to 25 lbs. and push/pull up to 40 lbs.
§ Ability to perform the following physical tasks: sitting, standing, stooping, stretching, walking, bending, twisting, reaching, performing repetitive motions, and carrying boxes.
Job Requirements
- Individuals applying must be a minimum twenty-one (21) years old
- Must have a valid driver’s license or ID.
- 2 years of experience in the cannabis industry; focusing specifically on inventory tracking systems.
- A State and Federal background check and pre-employment drug test.
- Advanced skills in METRC, Leaf Logix, Microsoft Suite, and computer systems.
- Certain situations require that work is completed on weekends, afterhours, and holidays.
Qualifications
- Compliance Oriented
- Possess high level of integrity
- Self-Starter: takes initiative to improve
- Critical thinker
- Step by step focused professional
- Organized data collector: ability to track data and trends
- Flexibility to pivot on tasks as directed.
- Proactive and self-organized
- Capable to work independently as well as in a team environment
- Ability to complete assigned tasks within the given time in order to meet deadlines
Job Type: Full-time
Pay: $18.00 per hour
Benefits:
- Dental insurance
- Health insurance
- Paid time off
- Vision insurance
Schedule:
- 8 hour shift
Work Location: One location
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Fazow accepts no liability or responsibility as a consequence of any reliance upon information on external sites or in jobs listed on fazow.com.
THE TEAM:
Founded in 2018 and headquartered in Boca Raton, Florida, Jushi is a vertically integrated, multi-state cannabis company that develops and operates high-end retail locations, premium brands, state-of-the-art cultivation, processing, manufacturing facilities, along with a cutting-edge online platform that is setting a new standard for a sophisticated, data-driven, modern cannabis experience.
Since its founding in 2018, Jushi has grown from just a handful of people with an idea to more than 900 employees strong. The Company has scaled its operations in seven states, including Pennsylvania, Virginia, Massachusetts, Illinois, California, Nevada, and Ohio, and has been named one of the top five cannabis companies to work for by Cannabis Business Times.
The Company operates more than two dozen retail locations across the country under the retail brand, BEYOND / HELLO™ as well as under the recently acquired brand, Nature’s Remedy. The Company provides an unparalleled in-store experience, coupled with online reservations and in-store express pickup.
Each day, Jushi team members continue to grow, cultivate, process and manufacture a comprehensive suite of cannabis brands under the names: The Bank, The Lab, Tasteology, Nira + Medicinals and Sèche, which are addressing a wide variety of consumer and patient needs across multiple states
THE OPPORTUNITY
Want to make a meaningful difference in peoples’ lives while earning a competitive salary? At Jushi, we are shaping the future of the cannabis industry, the fastest growing jobs sector in the U.S. The Quality Assurance (QA) Technician will be responsible for assisting in all quality aspects of the production site and ensure all products are manufactured in compliance with 21CFR111 requirements. The QA Technician is responsible for quality inspections of Medical Cannabis products and auditing the processes and procedures in the medical cannabis manufacturing operation. They are required to follow set processes and ensure adherence to state regulations, SOPs, work instructions (WI), and adhere to good manufacturing practices (GMP), good laboratory practices (GLP) and other product quality standards.
WHAT YOU WILL DO
Perform Quality Inspections on products, equipment, and procedures.- Responsible for monitoring cannabis product quality and safety throughout the manufacturing process.
- Responsible for performing verification of sanitation, equipment and other areas as required.
- Responsible for auditing the correct recording and filing of all relevant record logs and documentation completed by staff.
- Ensures the correct guidelines for production are followed during operations.
- Ensures employees are following all SOP’s, Work Instructions, and worker safety practices.
- Assist Quality Manager with instructing employees on Quality Improvements or Issues.
- Collect product samples for Product Development, lab retains and the laboratory when directed.
- May perform or assist inventory management personnel with inventory audits when needed.
- Support team members on quality management program to ensure there is an in-depth understanding of program and individual responsibilities.
- Provide support to GMP production operations, including conducting SOPs, training, and serve as resource to operations for quality controls and GMP compliance.
- Support improvement and alignment of the Quality Management Systems at site level.
- Conduct all duties in compliance with safety rules, applicable SOPs, and other relevant guidelines.
- Support all staff in data collection and analysis, reporting activities that support quality improvement interventions, transparency, compliance regulatory standards and provide performance monitoring.
- Support review and approval of batch record documentation, including validation protocols, master batch records, analytical test results, packaging, and labeling documentation.
EDUCATION & EXPERIENCE
Familiarity with FDA regulations and/or operating in a regulated environment preferred.- Attention to detail and ability to record numerical data and understand nomenclature and lot/Batch numbering systems.
- Ability to be flexible and provide support to any department within the organization as required by Operations leadership.
- Must be able to read and write in English and the ability to perform basic calculations.
- Microsoft Office skills.
- Must pass criminal background check.
PHYSICAL REQUIRMENTS
Regularly perform desk-based computer tasks- Frequently sitting and standing
- Occasionally Twist/bend/stoop/squat, kneel/crawl
- An environment with minimal noise levels
OTHER DUTIES
Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice
Jushi is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity or expression, religion, national origin or ancestry, age, disability, marital status, pregnancy, protected veteran status, protected genetic information, political affiliation, or any other characteristics protected by local laws, regulations, or ordinances.
We offer benefit packages that may include: Medical, Dental, Vision, Life, Short, and Long Term Disability, Flexible Spending Accounts, Paid Time Off, and Paid Holidays.
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Job title: Quality Assurance Technician
Reporting Location: Tampa, FL 33610 (10 Minutes away from Busch Gardens)
Key responsibilities:
- Wearing the appropriate PPE’s making sure that we are actively replacing the required PPEs in each specific situation/manufacturing room, at the correct frequency, to prevent cross contamination.
- Assures consistent quality of production by maintaining good manufacturing practice (GMP), validating all in-process checks real time, monitoring logs for accuracy and completion, documenting discrepancies, and completing accurate daily EOD reports.
- Communicating clear and real time in process updates, real status of project completion, prompt escalation of any issues.
- Teamwork, open communication, coordinate all work activities, including lunch breaks, emergencies, vacations, time off, with your peers, own your development, ask questions, take notes.
- Collaborate with manufacturing team making sure that In-process checks are being conducted in a timely manner.
Available hours: Full time Schedule
_____________________________________________________________________________
Cansortium Inc is a vertically integrated cultivator, processor, formulator, and retailer of Premium Cannabis Products currently operating in Florida, Pennsylvania, and Texas as Fluent Cannabis, as well as in Michigan through its in-market partner. Our purpose is to compassionately provide patients access to the highest level of medical cannabis in an unrivaled, professional healthcare environment with outstanding customer service. Patient care always comes first at Fluent, and our standards, practices, and performance is unmatched. We are looking for leaders who want to work alongside great talent and create a positive work experience for their team. We are focused on continuous improvements, which creates development opportunities, engaged feedback, and increased contributions towards our goals as a leader in the medical cannabis industry.
Find out more at www.getfluent.com. Follow us on LinkedIn.
ROLE SUMMARY
A Quality Assurance Technician I is responsible for assuring consistent production quality, enforcing good manufacturing practice (GMP), validating processes, assisting Tech II with improvements, verifying all documentation.
Hours 6:30AM - 7:15PM = Opener = 6:30AM-5:30PM, Closer = 7:30AM-7:15PM
Shift A – Sunday-Wednesday
Shift B - Wednesday-Saturday
KEY RESPONSIBILITIES
- Wearing the appropriate PPE’s making sure that we are actively replacing the required PPEs in each specific situation/manufacturing room, at the correct frequency, to prevent cross contamination.
- Assures consistent quality of production by maintaining good manufacturing practice (GMP), validating all in-process checks real time, monitoring logs for accuracy and completion, documenting discrepancies, and completing accurate daily EOD reports.
- Communicating clear and real time in process updates, real status of project completion, prompt escalation of any issues.
- Teamwork, open communication, coordinate all work activities, including lunch breaks, emergencies, vacations, time off, with your peers, own your development, ask questions, take notes.
- Collaborate with manufacturing team making sure that In-process checks are being conducted in a timely manner.
- Understand the requirements of internal Labels, how they correlate to project folders.
- Understanding Basic compliance of specific products, no storing any product on the floor, floor waste, and how to handle it, how to keep same product together, to prevent like products from being mixed.
- Identify all quality issues and report them to Tech 2.
- Primary person to manage moving products between rooms, to ensure efficient workflow and space management.
- Complete and accurate documentation of all required verification - checks and balances.
- Organization of product and cleanliness of all vault spaces, preventive maintenance of dehumidifiers.
- Safely lift all product, be able to load a cart and rack, ensuring that the packaging and bins are correctly interlocked, to protect the integrity of the product inside of it.
- Assure the quality of the product packaging and correctness and accuracy of product labeling.
- Moving all product physically from last manufacturing step to the appropriate vault and transferring the electronic custody in Biotrack.
- Assist with the preparation of lab testing paperwork, printing Lab labels, in an efficient manner prior to the arrival of third-party testing labs.
- Verifying and signing all manufacturing documentation in an efficient manner, as the project is completed, ensure the transfer is made, the file is closed.
- Accepting ownership, accomplishing new and different department goals, while exploring opportunities and adding value to departmental targets.
QUALIFICATIONS
- Bachelor of Science degree or related field experience
- Minimum two years of experience in a Quality Control, supporting Pharmaceutical, Manufacturing, or other regulated industry
- GMP knowledge with a focus in operational excellence in GMPs, recalls, electronic and hard copy records in an operational environment
- Experience with QA measuring and testing equipment
- Knowledge of safety requirements and legal standards
- Working knowledge of quality system requirements
- Experience with MS Word, Excel, Project Management, and Analytics software
- Analyzing information
- Tactical planning
- Great communication skills
- Emphasizing excellence
- Dealing with complexity
SKILLS
- Must be a multitasker, with the ability to work on several requests simultaneously without losing focus
- Organization and initiative, good communications skills, proactive, problem-solving, time management, discretion and confidentiality are essential attributes
- Excellent critical thinking and analytical skills
- Must possess an inquisitive and creative mind
- Ability to build good relationships. There will be frequent contact with internal team members, either face to face or by telephone or email
- Teamwork- collaborating with others to improve overall standards of work and service
- Thoroughness
REQUIRED EDUCATION and EXPERIENCE
- High School Diploma
ADDITIONAL REQUIREMENTS
Per state law, must be at least 21 years of age.
Must successfully complete a comprehensive background check.
Must pass a drug screening.
SUPERVISORY RESPONSIBILITIES
There are no supervisory responsibilities for this role
WORK ENVIRONMENT
This position operates in a manufacturing and distribution environment. This role uses standard office equipment such as computers/laptop, printers, phones, photocopiers, filing cabinets, fax machines, laminators.
PHYSICAL DEMANDS
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. While performing the duties of this job, the employee is regularly required to speak and hear. The employee frequently is required to stand for extended periods; walk; use hands to handle or feel objects, tools or controls; reach with hands and arms. Must be able to individually lift, up to 35 lbs, repeatably, through out the day. Push and Pull cart and large racks of material, from room to room, this may require two individuals, while Regular and predictable attendance is essential.
POSITION TYPE / EXPECTED HOURS OF WORK
This position regularly requires long hours and weekends as needed.
TRAVEL
Travel is primarily local during the business day, although some out-of-the-area and overnight travel may be expected.
OTHER DUTIES
Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice. The company will ask you to help in other departments depending on company needs. This means that you may not always work in the department that you were hired, teamwork and getting product out to patients is the goal and this means helping out where you are needed is crucial to your success as well as the company’s success.
AAP/EEO Statement
Fluent is an equal opportunity employer and we welcome applications from all backgrounds regardless of race, color, religion, sex, ancestry, age, marital status, sexual orientation, gender identity, disability or any other classification protected by law.
COMPANY BENEFITS
Fluent provides comprehensive benefits offerings to all full-time employees. Our benefits include medical, dental and vision and supplemental insurance, paid time-off program and non-matching 401k plan. All applicants must be legally authorized to work in the United States and will be required to submit proof of such eligibility.
Please note: Only shortlisted candidates will be contacted.
Keywords: Quality Assurance, Cannabis Industry, Medical Marijuana, Manufacturing
Apply for this job with Fluent Cannabis Care
Apply now →
By clicking the "Apply now" button, you'll be leaving Fazow and going to an external job application page for this company.
Please research all companies before applying. When applying for jobs, you should NOT have to pay to apply.
Fazow accepts no liability or responsibility as a consequence of any reliance upon information on external sites or in jobs listed on fazow.com.
COMPANY OVERVIEW
Recently named one of Entrepreneur magazine’s Top 100 Cannabis Leaders, Cresco Labs is one of the largest vertically-integrated multi-state cannabis operators in the United States. Cresco is built to become the most important company in the cannabis industry by combining the most strategic geographic footprint with one of the leading distribution platforms in North America. Employing a consumer-packaged goods (“CPG”) approach to cannabis, Cresco’s house of brands is designed to meet the needs of all consumer segments and includes some of the most recognized and trusted national brands including Cresco, Remedi and Mindy’s, a line of edibles created by James Beard Award-winning chef Mindy Segal. Sunnyside*, Cresco’s national dispensary brand is a wellness-focused retailer designed to build trust, education and convenience for both existing and new cannabis consumers. Recognizing that the cannabis industry is poised to become one of the leading job creators in the country, Cresco has launched the industry’s first national comprehensive Social Equity and Educational Development (SEED) initiative designed to ensure that all members of society have the skills, knowledge and opportunity to work in and own businesses in the cannabis industry.
MISSION STATEMENT
At Cresco, we aim to lead the nation’s cannabis industry with a focus on regulatory compliance, product consistency, and customer satisfaction. Our operations bring legitimacy to the cannabis industry by acting with the highest level of integrity, strictly adhering to regulations, and promoting the clinical efficacy of cannabis. As Cresco grows, we will operate with the same level of professionalism and precision in each new market we move in to.
JOB SUMMARY
Cresco Labs is seeking a Quality Assurance (QA) Technician to join our manufacturing team in Mendota, CA. As a QA Technician, you will be responsible for assisting with quality-related activities at the facility associated with incoming inspection, start-up verification, in-process verifications & checks, and sampling and inspection of finished products. Product families could include cannabis flower, cannabis oil, manufacturing infused products (vape pens/cartridges), and food products (gummies). This position will also help ensure products are being produced in a manner that meets all specifications and brand consistency. You will also assist in identifying potential quality risks and working with operations personnel to develop improvement opportunities. The ideal candidate must possess a strong attention to detail and experience working within a highly regulated industry.
CORE JOB DUTIES
- Performs incoming inspections
- Performs finished product sampling and inspection
- Maintains retain library
- Performs equipment and product line clearances before processing/production runs including but not limited to cleaning and sanitation verification, metal detector checks, and balance checks.
- Performs regulatory label review and approval prior to start-up
- Performs in-process verifications to ensure product weights, correct labeling & packaging for transfer.
- Performs in-process ANSI inspections.
- Performs verifications on finished product including but not limited to metal detection checks, label review, and record review.
- Assists in customer complaints and product investigations, helping to assess risk, identify root cause and quarantine product.
- Inspects packaged orders to ensure correct content and quantities, as deemed necessary.
- Reviews in-process batch documentation to ensure real-time compliance to product specifications, good documentation practices and written policies/procedures.
- Monitors compliance to established Good Manufacturing Practice (GMP) guidance.
- Reviews product quality standards and specifications to make sure they are available during production runs.
- Complete all required trainings on time.
- Conducts all duties in compliance with safety rules, applicable SOPs, and other applicable guidelines.
- Other duties as assigned
- May require travel to other states or facilities to assist with inspections or quality issues.
REQUIRED EXPERIENCE, EDUCATION AND SKILLS
- Bachelors Degree, or 1-2 years experience and an Associate Degree, or 2+ years experience in a production environment
- Prior experience in a highly regulated industry. Highly desirable: healthcare, medical devices, pharmaceutical, consumer packaged goods (food), FDA, HACCP, or SQ.
- Prior experience in Quality Assurance or Quality Control function desired
- Prior experience with product sampling, inspection procedures, customer complaints, product investigations, and CAPA desired
- Ability to follow written procedures and monitor others for adherence to written procedures
- Ability to create or update written procedures with site operations personnel, as needed
- Strong written and verbal communication skills
- Detail-oriented
- Utilizes critical thinking to troubleshoot issues, work collaboratively with a team to brainstorm solutions, and implement solutions
- Desired – bi-lingual in Spanish and English
BENEFITS
Cresco Labs is proud to offer eligible employees a robust offering of benefits including, major medical, dental and vision insurance, a 401(K)-match program, FSA/HSA programs, LTD/STD options, life insurance and AD&D. We also offer eligible employees paid holidays and paid time off. Other rewards may include annual discretionary bonuses, stock options as well as participation in our employee discount program. Benefits eligibility for permanent positions may vary by full-time or part-time roles, location, or position.
ADDITIONAL REQUIREMENTS
- Must be 21 years of age or older to apply
- Must comply with all legal or company regulations for working in the industry
Cresco Labs is an Equal Opportunity Employer and all applicants will be considered without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status.
Job Type: Full-time
Pay: $22.12 per hour
Benefits:
- 401(k) matching
- Dental insurance
- Health insurance
- Life insurance
- Paid time off
- Parental leave
- Vision insurance
Schedule:
- 8 hour shift
Ability to commute/relocate:
- Mendota, CA 93640: Reliably commute or planning to relocate before starting work (Required)
Experience:
- Manufacturing: 1 year (Preferred)
Work Location: One location
Apply for this job with Cresco Labs, LLC
Apply now →
By clicking the "Apply now" button, you'll be leaving Fazow and going to an external job application page for this company.
Please research all companies before applying. When applying for jobs, you should NOT have to pay to apply.
Fazow accepts no liability or responsibility as a consequence of any reliance upon information on external sites or in jobs listed on fazow.com.
COMPANY OVERVIEW
Recently named one of Entrepreneur magazine's Top 100 Cannabis Leaders, Cresco Labs is one of the largest vertically-integrated multi-state cannabis operators in the United States. Cresco is built to become the most important company in the cannabis industry by combining the most strategic geographic footprint with one of the leading distribution platforms in North America. Employing a consumer-packaged goods ("CPG") approach to cannabis, Cresco's house of brands is designed to meet the needs of all consumer segments and includes some of the most recognized and trusted national brands including Cresco, Remedi and Mindy's, a line of edibles created by James Beard Award-winning chef Mindy Segal. Sunnyside*, Cresco's national dispensary brand is a wellness-focused retailer designed to build trust, education and convenience for both existing and new cannabis consumers. Recognizing that the cannabis industry is poised to become one of the leading job creators in the country, Cresco has launched the industry's first national comprehensive Social Equity and Educational Development (SEED) initiative designed to ensure that all members of society have the skills, knowledge and opportunity to work in and own businesses in the cannabis industry.
MISSION STATEMENT
At Cresco, we aim to lead the nation's cannabis industry with a focus on regulatory compliance, product consistency, and customer satisfaction. Our operations bring legitimacy to the cannabis industry by acting with the highest level of integrity, strictly adhering to regulations, and promoting the clinical efficacy of cannabis. As Cresco grows, we will operate with the same level of professionalism and precision in each new market we move in to.
JOB SUMMARY
Cresco Labs is seeking a Quality Assurance (QA) Technician to join our manufacturing team in Mendota, CA. As a QA Technician, you will be responsible for assisting with quality-related activities at the facility associated with incoming inspection, start-up verification, in-process verifications & checks, and sampling and inspection of finished products. Product families could include cannabis flower, cannabis oil, manufacturing infused products (vape pens/cartridges), and food products (gummies). This position will also help ensure products are being produced in a manner that meets all specifications and brand consistency. You will also assist in identifying potential quality risks and working with operations personnel to develop improvement opportunities. The ideal candidate must possess a strong attention to detail and experience working within a highly regulated industry.
CORE JOB DUTIES
- Performs incoming inspections
- Performs finished product sampling and inspection
- Maintains retain library
- Performs equipment and product line clearances before processing/production runs including but not limited to cleaning and sanitation verification, metal detector checks, and balance checks.
- Performs regulatory label review and approval prior to start-up
- Performs in-process verifications to ensure product weights, correct labeling & packaging for transfer.
- Performs in-process ANSI inspections.
- Performs verifications on finished product including but not limited to metal detection checks, label review, and record review.
- Assists in customer complaints and product investigations, helping to assess risk, identify root cause and quarantine product.
- Inspects packaged orders to ensure correct content and quantities, as deemed necessary.
- Reviews in-process batch documentation to ensure real-time compliance to product specifications, good documentation practices and written policies/procedures.
- Monitors compliance to established Good Manufacturing Practice (GMP) guidance.
- Reviews product quality standards and specifications to make sure they are available during production runs.
- Complete all required trainings on time.
- Conducts all duties in compliance with safety rules, applicable SOPs, and other applicable guidelines.
- Other duties as assigned
- May require travel to other states or facilities to assist with inspections or quality issues.
REQUIRED EXPERIENCE, EDUCATION AND SKILLS
- Bachelors Degree, or 1-2 years experience and an Associate Degree, or 2+ years experience in a production environment
- Prior experience in a highly regulated industry. Highly desirable: healthcare, medical devices, pharmaceutical, consumer packaged goods (food), FDA, HACCP, or SQ.
- Prior experience in Quality Assurance or Quality Control function desired
- Prior experience with product sampling, inspection procedures, customer complaints, product investigations, and CAPA desired
- Ability to follow written procedures and monitor others for adherence to written procedures
- Ability to create or update written procedures with site operations personnel, as needed
- Strong written and verbal communication skills
- Detail-oriented
- Utilizes critical thinking to troubleshoot issues, work collaboratively with a team to brainstorm solutions, and implement solutions
- Desired – bi-lingual in Spanish and English
BENEFITS
Cresco Labs is proud to offer eligible employees a robust offering of benefits including, major medical, dental and vision insurance, a 401(K)-match program, FSA/HSA programs, LTD/STD options, life insurance and AD&D. We also offer eligible employees paid holidays and paid time off. Other rewards may include annual discretionary bonuses, stock options as well as participation in our employee discount program. Benefits eligibility for permanent positions may vary by full-time or part-time roles, location, or position.
ADDITIONAL REQUIREMENTS
- Must be 21 years of age or older to apply
- Must comply with all legal or company regulations for working in the industry
Cresco Labs is an Equal Opportunity Employer and all applicants will be considered without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status.
Apply for this job with Cresco Labs
Apply now →
By clicking the "Apply now" button, you'll be leaving Fazow and going to an external job application page for this company.
Please research all companies before applying. When applying for jobs, you should NOT have to pay to apply.
Fazow accepts no liability or responsibility as a consequence of any reliance upon information on external sites or in jobs listed on fazow.com.
THE TEAM:
Founded in 2018 and headquartered in Boca Raton, Florida, Jushi is a vertically integrated, multi-state cannabis company that develops and operates high-end retail locations, premium brands, state-of-the-art cultivation, processing, manufacturing facilities, along with a cutting-edge online platform that is setting a new standard for a sophisticated, data-driven, modern cannabis experience.
Since its founding in 2018, Jushi has grown from just a handful of people with an idea to more than 900 employees strong. The Company has scaled its operations in seven states, including Pennsylvania, Virginia, Massachusetts, Illinois, California, Nevada, and Ohio, and has been named one of the top five cannabis companies to work for by Cannabis Business Times.
The Company operates more than two dozen retail locations across the country under the retail brand, BEYOND / HELLO™ as well as under the recently acquired brand, Nature’s Remedy. The Company provides an unparalleled in-store experience, coupled with online reservations and in-store express pickup.
Each day, Jushi team members continue to grow, cultivate, process and manufacture a comprehensive suite of cannabis brands under the names: The Bank, The Lab, Tasteology, Nira + Medicinals and Sèche, which are addressing a wide variety of consumer and patient needs across multiple states
THE OPPORTUNITY
Want to make a meaningful difference in peoples’ lives while earning a competitive salary? At Jushi, we are shaping the future of the cannabis industry, the fastest growing jobs sector in the U.S. The Quality Assurance (QA) Technician will be responsible for assisting in all quality aspects of the production site and ensure all products are manufactured in compliance with 21CFR111 requirements. The QA Technician is responsible for quality inspections of Medical Cannabis products and auditing the processes and procedures in the medical cannabis manufacturing operation. They are required to follow set processes and ensure adherence to state regulations, SOPs, work instructions (WI), and adhere to good manufacturing practices (GMP), good laboratory practices (GLP) and other product quality standards.
WHAT YOU WILL DO
- Perform Quality Inspections on products, equipment, and procedures.
- Responsible for monitoring cannabis product quality and safety throughout the manufacturing process.
- Responsible for performing verification of sanitation, equipment and other areas as required.
- Responsible for auditing the correct recording and filing of all relevant record logs and documentation completed by staff.
- Ensures the correct guidelines for production are followed during operations.
- Ensures employees are following all SOP’s, Work Instructions, and worker safety practices.
- Assist Quality Manager with instructing employees on Quality Improvements or Issues.
- Collect product samples for Product Development, lab retains and the laboratory when directed.
- May perform or assist inventory management personnel with inventory audits when needed.
- Support team members on quality management program to ensure there is an in-depth understanding of program and individual responsibilities.
- Provide support to GMP production operations, including conducting SOPs, training, and serve as resource to operations for quality controls and GMP compliance.
- Support improvement and alignment of the Quality Management Systems at site level.
- Conduct all duties in compliance with safety rules, applicable SOPs, and other relevant guidelines.
- Support all staff in data collection and analysis, reporting activities that support quality improvement interventions, transparency, compliance regulatory standards and provide performance monitoring.
- Support review and approval of batch record documentation, including validation protocols, master batch records, analytical test results, packaging, and labeling documentation.
EDUCATION & EXPERIENCE
- Familiarity with FDA regulations and/or operating in a regulated environment preferred.
- Attention to detail and ability to record numerical data and understand nomenclature and lot/Batch numbering systems.
- Ability to be flexible and provide support to any department within the organization as required by Operations leadership.
- Must be able to read and write in English and the ability to perform basic calculations.
- Microsoft Office skills.
- Must pass criminal background check.
PHYSICAL REQUIRMENTS
- Regularly perform desk-based computer tasks
- Frequently sitting and standing
- Occasionally Twist/bend/stoop/squat, kneel/crawl
- An environment with minimal noise levels
OTHER DUTIES
Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice
Jushi is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity or expression, religion, national origin or ancestry, age, disability, marital status, pregnancy, protected veteran status, protected genetic information, political affiliation, or any other characteristics protected by local laws, regulations, or ordinances.
We offer benefit packages that may include: Medical, Dental, Vision, Life, Short, and Long Term Disability, Flexible Spending Accounts, Paid Time Off, and Paid Holidays.
Job Type: Full-time
Schedule:
- 8 hour shift
Ability to commute/relocate:
- Lakeville, MA: Reliably commute or planning to relocate before starting work (Required)
Experience:
- Manufacturing: 1 year (Preferred)
Work Location: One location
Apply for this job with Jushi
Apply now →
By clicking the "Apply now" button, you'll be leaving Fazow and going to an external job application page for this company.
Please research all companies before applying. When applying for jobs, you should NOT have to pay to apply.
Fazow accepts no liability or responsibility as a consequence of any reliance upon information on external sites or in jobs listed on fazow.com.
THE TEAM:
Founded in 2018 and headquartered in Boca Raton, Florida, Jushi is a vertically integrated, multi-state cannabis company that develops and operates high-end retail locations, premium brands, state-of-the-art cultivation, processing, manufacturing facilities, along with a cutting-edge online platform that is setting a new standard for a sophisticated, data-driven, modern cannabis experience.
Since its founding in 2018, Jushi has grown from just a handful of people with an idea to more than 900 employees strong. The Company has scaled its operations in seven states, including Pennsylvania, Virginia, Massachusetts, Illinois, California, Nevada, and Ohio, and has been named one of the top five cannabis companies to work for by Cannabis Business Times.
The Company operates more than two dozen retail locations across the country under the retail brand, BEYOND / HELLO™ as well as under the recently acquired brand, Nature’s Remedy. The Company provides an unparalleled in-store experience, coupled with online reservations and in-store express pickup.
Each day, Jushi team members continue to grow, cultivate, process and manufacture a comprehensive suite of cannabis brands under the names: The Bank, The Lab, Tasteology, Nira + Medicinals and Sèche, which are addressing a wide variety of consumer and patient needs across multiple states
THE OPPORTUNITY
Want to make a meaningful difference in peoples’ lives while earning a competitive salary? At Jushi, we are shaping the future of the cannabis industry, the fastest growing jobs sector in the U.S. The Quality Assurance (QA) Technician will be responsible for assisting in all quality aspects of the production site and ensure all products are manufactured in compliance with 21CFR111 requirements. The QA Technician is responsible for quality inspections of Medical Cannabis products and auditing the processes and procedures in the medical cannabis manufacturing operation. They are required to follow set processes and ensure adherence to state regulations, SOPs, work instructions (WI), and adhere to good manufacturing practices (GMP), good laboratory practices (GLP) and other product quality standards.
WHAT YOU WILL DO
Perform Quality Inspections on products, equipment, and procedures.- Responsible for monitoring cannabis product quality and safety throughout the manufacturing process.
- Responsible for performing verification of sanitation, equipment and other areas as required.
- Responsible for auditing the correct recording and filing of all relevant record logs and documentation completed by staff.
- Ensures the correct guidelines for production are followed during operations.
- Ensures employees are following all SOP’s, Work Instructions, and worker safety practices.
- Assist Quality Manager with instructing employees on Quality Improvements or Issues.
- Collect product samples for Product Development, lab retains and the laboratory when directed.
- May perform or assist inventory management personnel with inventory audits when needed.
- Support team members on quality management program to ensure there is an in-depth understanding of program and individual responsibilities.
- Provide support to GMP production operations, including conducting SOPs, training, and serve as resource to operations for quality controls and GMP compliance.
- Support improvement and alignment of the Quality Management Systems at site level.
- Conduct all duties in compliance with safety rules, applicable SOPs, and other relevant guidelines.
- Support all staff in data collection and analysis, reporting activities that support quality improvement interventions, transparency, compliance regulatory standards and provide performance monitoring.
- Support review and approval of batch record documentation, including validation protocols, master batch records, analytical test results, packaging, and labeling documentation.
EDUCATION & EXPERIENCE
Familiarity with FDA regulations and/or operating in a regulated environment preferred.- Attention to detail and ability to record numerical data and understand nomenclature and lot/Batch numbering systems.
- Ability to be flexible and provide support to any department within the organization as required by Operations leadership.
- Must be able to read and write in English and the ability to perform basic calculations.
- Microsoft Office skills.
- Must pass criminal background check.
PHYSICAL REQUIRMENTS
Regularly perform desk-based computer tasks- Frequently sitting and standing
- Occasionally Twist/bend/stoop/squat, kneel/crawl
- An environment with minimal noise levels
OTHER DUTIES
Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice
Jushi is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity or expression, religion, national origin or ancestry, age, disability, marital status, pregnancy, protected veteran status, protected genetic information, political affiliation, or any other characteristics protected by local laws, regulations, or ordinances.
We offer benefit packages that may include: Medical, Dental, Vision, Life, Short, and Long Term Disability, Flexible Spending Accounts, Paid Time Off, and Paid Holidays.
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COMPANY OVERVIEW
Recently named one of Entrepreneur magazine's Top 100 Cannabis Leaders, Cresco Labs is one of the largest vertically-integrated multi-state cannabis operators in the United States. Cresco is built to become the most important company in the cannabis industry by combining the most strategic geographic footprint with one of the leading distribution platforms in North America. Employing a consumer-packaged goods ("CPG") approach to cannabis, Cresco's house of brands is designed to meet the needs of all consumer segments and includes some of the most recognized and trusted national brands including Cresco, Remedi and Mindy's, a line of edibles created by James Beard Award-winning chef Mindy Segal. Sunnyside*, Cresco's national dispensary brand is a wellness-focused retailer designed to build trust, education and convenience for both existing and new cannabis consumers. Recognizing that the cannabis industry is poised to become one of the leading job creators in the country, Cresco has launched the industry's first national comprehensive Social Equity and Educational Development (SEED) initiative designed to ensure that all members of society have the skills, knowledge and opportunity to work in and own businesses in the cannabis industry.
MISSION STATEMENT
At Cresco, we aim to lead the nation's cannabis industry with a focus on regulatory compliance, product consistency, and customer satisfaction. Our operations bring legitimacy to the cannabis industry by acting with the highest level of integrity, strictly adhering to regulations, and promoting the clinical efficacy of cannabis. As Cresco grows, we will operate with the same level of professionalism and precision in each new market we move in to.
JOB SUMMARY
Cresco Labs is seeking a Quality Assurance (QA) Technician to join our manufacturing team in Sacramento, CA. As a QA Technician, you will be responsible for assisting with quality-related activities at the facility associated with incoming inspection, start-up verification, in-process verifications & checks, and sampling and inspection of finished products. Product families could include cannabis flower, cannabis oil, manufacturing infused products (lotion, capsules, vape pens/cartridges, transdermal patches), and food products (chocolate, gummies, cookies). This position will also help ensure products are being produced in a manner that meets all specifications and brand consistency. You will also assist in identifying potential quality risks and working with operations personnel to develop improvement opportunities. The ideal candidate must possess a strong attention to detail and experience working within a highly regulated industry.
CORE JOB DUTIES
- Performs incoming inspections, as needed
- Performs finished product sampling and inspection.
- Performs equipment and product line clearances before processing/production runs.
- Performs in-process verifications to ensure product weights, correct labeling & packaging for transfer.
- Performs verifications on finished product with metal detection or x-ray, as deemed necessary.
- Assists in customer complaints and product investigations, helping to assess risk, identify root cause and quarantine product.
- Inspects packaged orders to ensure correct content and quantities, as deemed necessary.
- Reviews in-process batch documentation to ensure real-time compliance to product specifications, good documentation practices and written policies/procedures.
- Monitors compliance to established Good Manufacturing Practice (GMP) guidance.
- Conducts all duties in compliance with safety rules, applicable SOPs, and other applicable guidelines.
- May require travel to other states or facilities to assist with inspections or quality issues.
REQUIRED EXPERIENCE, EDUCATION AND SKILLS
- Bachelors Degree, 1-3 years experience or Associate Degree, 5+ years experience
- Prior experience in highly regulated industry. Highly desirable: cannabis, healthcare, medical devices, pharmaceutical, consumer packaged goods (food). Highly desirable: Cannabis, FDA, HACCP, SQF experience
- Prior experience in Quality Assurance or Quality Control function
- Prior experience with product sampling, inspection procedures, customer complaints, product investigations, and CAPA desired
- Ability to follow written procedures and monitor others for adherence to written procedures
- Ability to create or update written procedures with site operations personnel, as needed
- Strong written and verbal communication skills
- Detail-oriented
- Utilizes critical thinking to troubleshoot issues, work collaboratively with a team to brainstorm solutions, and implement improvement solutions
BENEFITS
Cresco Labs is proud to offer eligible employees a robust offering of benefits including, major medical, dental and vision insurance, a 401(K)-match program, FSA/HSA programs, LTD/STD options, life insurance and AD&D. We also offer eligible employees paid holidays and paid time off. Other rewards may include annual discretionary bonuses, stock options as well as participation in our employee discount program. Benefits eligibility for permanent positions may vary by full-time or part-time roles, location, or position.
ADDITIONAL REQUIREMENTS
- Must be 21 years of age or older to apply
- Must comply with all legal or company regulations for working in the industry
Cresco Labs is an Equal Opportunity Employer and all applicants will be considered without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status.
Apply for this job with Cresco Labs
Apply now →
By clicking the "Apply now" button, you'll be leaving Fazow and going to an external job application page for this company.
Please research all companies before applying. When applying for jobs, you should NOT have to pay to apply.
Fazow accepts no liability or responsibility as a consequence of any reliance upon information on external sites or in jobs listed on fazow.com.
COMPANY OVERVIEW
Recently named one of Entrepreneur magazine’s Top 100 Cannabis Leaders, Cresco Labs is one of the largest vertically-integrated multi-state cannabis operators in the United States. Cresco is built to become the most important company in the cannabis industry by combining the most strategic geographic footprint with one of the leading distribution platforms in North America. Employing a consumer-packaged goods (“CPG”) approach to cannabis, Cresco’s house of brands is designed to meet the needs of all consumer segments and includes some of the most recognized and trusted national brands including Cresco, Remedi and Mindy’s, a line of edibles created by James Beard Award-winning chef Mindy Segal. Sunnyside*, Cresco’s national dispensary brand is a wellness-focused retailer designed to build trust, education and convenience for both existing and new cannabis consumers. Recognizing that the cannabis industry is poised to become one of the leading job creators in the country, Cresco has launched the industry’s first national comprehensive Social Equity and Educational Development (SEED) initiative designed to ensure that all members of society have the skills, knowledge and opportunity to work in and own businesses in the cannabis industry.
MISSION STATEMENT
At Cresco, we aim to lead the nation’s cannabis industry with a focus on regulatory compliance, product consistency, and customer satisfaction. Our operations bring legitimacy to the cannabis industry by acting with the highest level of integrity, strictly adhering to regulations, and promoting the clinical efficacy of cannabis. As Cresco grows, we will operate with the same level of professionalism and precision in each new market we move in to.
JOB SUMMARY
Cresco Labs is seeking a Quality Assurance (QA) Technician to join our manufacturing team in Sacramento, CA. As a QA Technician, you will be responsible for assisting with quality-related activities at the facility associated with incoming inspection, start-up verification, in-process verifications & checks, and sampling and inspection of finished products. Product families could include cannabis flower, cannabis oil, manufacturing infused products (lotion, capsules, vape pens/cartridges, transdermal patches), and food products (chocolate, gummies, cookies). This position will also help ensure products are being produced in a manner that meets all specifications and brand consistency. You will also assist in identifying potential quality risks and working with operations personnel to develop improvement opportunities. The ideal candidate must possess a strong attention to detail and experience working within a highly regulated industry.
CORE JOB DUTIES
- Performs incoming inspections, as needed
- Performs finished product sampling and inspection.
- Performs equipment and product line clearances before processing/production runs.
- Performs in-process verifications to ensure product weights, correct labeling & packaging for transfer.
- Performs verifications on finished product with metal detection or x-ray, as deemed necessary.
- Assists in customer complaints and product investigations, helping to assess risk, identify root cause and quarantine product.
- Inspects packaged orders to ensure correct content and quantities, as deemed necessary.
- Reviews in-process batch documentation to ensure real-time compliance to product specifications, good documentation practices and written policies/procedures.
- Monitors compliance to established Good Manufacturing Practice (GMP) guidance.
- Conducts all duties in compliance with safety rules, applicable SOPs, and other applicable guidelines.
- May require travel to other states or facilities to assist with inspections or quality issues.
REQUIRED EXPERIENCE, EDUCATION AND SKILLS
- Bachelors Degree, 1-3 years experience or Associate Degree, 5+ years experience
- Prior experience in highly regulated industry. Highly desirable: cannabis, healthcare, medical devices, pharmaceutical, consumer packaged goods (food). Highly desirable: Cannabis, FDA, HACCP, SQF experience
- Prior experience in Quality Assurance or Quality Control function
- Prior experience with product sampling, inspection procedures, customer complaints, product investigations, and CAPA desired
- Ability to follow written procedures and monitor others for adherence to written procedures
- Ability to create or update written procedures with site operations personnel, as needed
- Strong written and verbal communication skills
- Detail-oriented
- Utilizes critical thinking to troubleshoot issues, work collaboratively with a team to brainstorm solutions, and implement improvement solutions
ADDITIONAL REQUIREMENTS
- Must be 21 years of age or older to apply
- Must comply with all legal or company regulations for working in the industry
Cresco Labs is an Equal Opportunity Employer and all applicants will be considered without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status.
Job Type: Full-time
Pay: $20.00 per hour
Benefits:
- 401(k) matching
- Dental insurance
- Health insurance
- Life insurance
- Paid time off
- Vision insurance
Schedule:
- 8 hour shift
- Monday to Friday
Ability to commute/relocate:
- Sacramento, CA: Reliably commute or planning to relocate before starting work (Preferred)
Education:
- Associate (Preferred)
Experience:
- QA/QC: 1 year (Preferred)
Work Location: One location
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As a Quality Assurance (QA) Technician, you will be responsible for assisting with quality-related activities including start-up verification, in-process verification & checks, BMR and documentation reviews, sampling, and inspection of finished products. Products include cannabis flower, cannabis oil, infused products (concentrates, capsules, lotions, tinctures, vapes, etc.) and food products (chocolate, gummies, lozenges, etc.). This position will also help ensure products are being produced in a manner that meets all specifications and brand consistency. You will also assist in identifying potential quality risks and working with operations personnel to develop improvement opportunities. The ideal candidate must possess a strong attention to detail and experience working within a highly regulated industry.
Job Summary and Responsibilities:
- Performs finished product sampling and inspection
- Performs equipment and product line clearances before production runs
- Performs in-process verification to ensure product weights, correct labeling & packaging
- Performs verification on finished products
- Inspects retain samples and customer return samples, as deemed necessary
- Assists in customer complaints and product investigations, helping to assess risk, identify root cause and quarantine product
- Inspects packaged orders to ensure correct content and quantities, as deemed necessary
- Reviews in-process batch documentation to ensure real-time compliance to product specifications, good documentation practices and written policies/procedures
- Monitors compliance to established Good Manufacturing Practice (GMP) and Safe Quality Foods guidance
- Conducts all duties in compliance with safety rules, applicable SOPs, and other applicable guidelines
- May require travel to other states or facilities to assist with inspections or quality issues
Required Experience, Education and Skills:
- Bachelors Degree, 1-3 years’ experience or Associate Degree, 5+ years’ experience
- Prior experience in highly regulated industry. Highly desirable: healthcare, medical devices, pharmaceutical, consumer packaged goods (food), cannabis. Highly desirable: FDA, HACCP, SQF experience
- Prior experience in Quality Assurance or Quality Control function
- Prior experience with product sampling, inspection procedures, customer complaints, product investigations, and CAPA
- Ability to follow written procedures and monitor others for adherence to written procedures
- Ability to create or update written procedures with site operations personnel
- Strong written and verbal communication skills
- Detail-oriented
- Utilizes critical thinking to troubleshoot issues, work collaboratively with a team to brainstorm solutions, and implement improvement solutions
- Must be flexible and able to work long hours and weekends as required
- Able to adapt in a quick and positive manner
- Able to work in a fast-paced environment and handle multiple tasks and requests
Additional Requirements:
- Must be 21 years of age or older
- Must comply with all legal and company regulations for working in the industry
- Ability to stand throughout extended periods, must be capable of squatting, standing, kneeling, bending, or walking throughout the workday
- Excellent communication skills and leadership both verbally and through written media.
- Strong decision-making, analytical and organizational skills
- Thorough understanding of state and local medical marijuana laws and how they apply to the operations
- COVID-19 considerations: For the safety of you and the team, we require proof of COVID-19 vaccination before hire.
Physical Demands:
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.
While performing the duties of this Job, the employee is regularly required to stand for extended periods every day. The employee must regularly lift and /or move up to 25 pounds, frequently lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus. Able to work 6 days a week and evening shifts if required.
Work Environment:
While performing the duties of this job, the employee will be standing indoors and frequently exposed to laboratory conditions. The employee is frequently exposed to fumes or airborne particles; toxic or caustic chemicals; and varying temperatures. The noise level in the work environment is usually loud.
Job Type: Full-time
Benefits:
- Dental insurance
- Employee discount
- Health insurance
- Paid time off
- Vision insurance
Schedule:
- 10 hour shift
- 12 hour shift
- 8 hour shift
- Day shift
- Night shift
- Overtime
- Weekend availability
Work Location: One location
Apply for this job with VidaCann
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By clicking the "Apply now" button, you'll be leaving Fazow and going to an external job application page for this company.
Please research all companies before applying. When applying for jobs, you should NOT have to pay to apply.
Fazow accepts no liability or responsibility as a consequence of any reliance upon information on external sites or in jobs listed on fazow.com.
COMPANY OVERVIEW
MISSION STATEMENT
Recently named one of Entrepreneur magazine's Top 100 Cannabis Leaders, Cresco Labs is one of the largest vertically-integrated multi-state cannabis operators in the United States. Cresco is built to become the most important company in the cannabis industry by combining the most strategic geographic footprint with one of the leading distribution platforms in North America. Employing a consumer-packaged goods ("CPG") approach to cannabis, Cresco's house of brands is designed to meet the needs of all consumer segments and includes some of the most recognized and trusted national brands including Cresco, Remedi and Mindy's, a line of edibles created by James Beard Award-winning chef Mindy Segal. Sunnyside*, Cresco's national dispensary brand is a wellness-focused retailer designed to build trust, education and convenience for both existing and new cannabis consumers. Recognizing that the cannabis industry is poised to become one of the leading job creators in the country, Cresco has launched the industry's first national comprehensive Social Equity and Educational Development (SEED) initiative designed to ensure that all members of society have the skills, knowledge and opportunity to work in and own businesses in the cannabis industry.
MISSION STATEMENT
At Cresco, we aim to lead the nation's cannabis industry with a focus on regulatory compliance, product consistency, and customer satisfaction. Our operations bring legitimacy to the cannabis industry by acting with the highest level of integrity, strictly adhering to regulations, and promoting the clinical efficacy of cannabis. As Cresco grows, we will operate with the same level of professionalism and precision in each new market we move in to.
JOB SUMMARY
Cresco Labs is seeking a Quality Assurance (QA) Technician to join our manufacturing team in Lincoln, Illinois. As a QA Technician, you will be responsible for assisting with quality-related activities at the facility associated with incoming inspection, start-up verification, in-process verifications & checks, and sampling and inspection of finished products. Product families could include cannabis flower, cannabis oil, manufacturing infused products (lotion, capsules, vape pens/cartridges, transdermal patches), and food products (chocolate, gummies, cookies). This position will also help ensure products are being produced in a manner that meets all specifications and brand consistency. You will also assist in identifying potential quality risks and working with operations personnel to develop improvement opportunities. The ideal candidate must possess a strong attention to detail and experience working within a highly regulated industry.
CORE JOB DUTIES
- Performs incoming inspections, as needed
- Performs finished product sampling and inspection.
- Performs equipment and product line clearances before processing/production runs.
- Performs in-process verifications to ensure product weights, correct labeling & packaging for transfer.
- Performs verifications on finished product with metal detection or x-ray, as deemed necessary.
- Assists in customer complaints and product investigations, helping to assess risk, identify root cause and quarantine product.
- Inspects packaged orders to ensure correct content and quantities, as deemed necessary.
- Reviews in-process batch documentation to ensure real-time compliance to product specifications, good documentation practices and written policies/procedures.
- Monitors compliance to established Good Manufacturing Practice (GMP) guidance.
- Conducts all duties in compliance with safety rules, applicable SOPs, and other applicable guidelines.
- May require travel to other states or facilities to assist with inspections or quality issues.
REQUIRED EXPERIENCE, EDUCATION AND SKILLS
- Bachelors Degree, 1-3 years experience or Associate Degree, 5+ years experience
- Prior experience in highly regulated industry. Highly desirable: cannabis, healthcare, medical devices, pharmaceutical, consumer packaged goods (food). Highly desirable: Cannabis, FDA, HACCP, SQF experience
- Prior experience in Quality Assurance or Quality Control function
- Prior experience with product sampling, inspection procedures, customer complaints, product investigations, and CAPA desired
- Ability to follow written procedures and monitor others for adherence to written procedures
- Ability to create or update written procedures with site operations personnel, as needed
- Strong written and verbal communication skills
- Detail-oriented
- Utilizes critical thinking to troubleshoot issues, work collaboratively with a team to brainstorm solutions, and implement improvement solutions
ADDITIONAL REQUIREMENTS
- Must be 21 years of age or older to apply
- Must comply with all legal or company regulations for working in the industry
Cresco Labs is an Equal Opportunity Employer and all applicants will be considered without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status.
Apply for this job with Cresco Labs
Apply now →
By clicking the "Apply now" button, you'll be leaving Fazow and going to an external job application page for this company.
Please research all companies before applying. When applying for jobs, you should NOT have to pay to apply.
Fazow accepts no liability or responsibility as a consequence of any reliance upon information on external sites or in jobs listed on fazow.com.
COMPANY OVERVIEW
MISSION STATEMENT
Recently named one of Entrepreneur magazine's Top 100 Cannabis Leaders, Cresco Labs is one of the largest vertically-integrated multi-state cannabis operators in the United States. Cresco is built to become the most important company in the cannabis industry by combining the most strategic geographic footprint with one of the leading distribution platforms in North America. Employing a consumer-packaged goods ("CPG") approach to cannabis, Cresco's house of brands is designed to meet the needs of all consumer segments and includes some of the most recognized and trusted national brands including Cresco, Remedi and Mindy's, a line of edibles created by James Beard Award-winning chef Mindy Segal. Sunnyside*, Cresco's national dispensary brand is a wellness-focused retailer designed to build trust, education and convenience for both existing and new cannabis consumers. Recognizing that the cannabis industry is poised to become one of the leading job creators in the country, Cresco has launched the industry's first national comprehensive Social Equity and Educational Development (SEED) initiative designed to ensure that all members of society have the skills, knowledge and opportunity to work in and own businesses in the cannabis industry.
MISSION STATEMENT
At Cresco, we aim to lead the nation's cannabis industry with a focus on regulatory compliance, product consistency, and customer satisfaction. Our operations bring legitimacy to the cannabis industry by acting with the highest level of integrity, strictly adhering to regulations, and promoting the clinical efficacy of cannabis. As Cresco grows, we will operate with the same level of professionalism and precision in each new market we move in to.
JOB SUMMARY
Cresco Labs is seeking a Quality Assurance (QA) Technician to join our manufacturing team in Sacramento, CA. As a QA Technician, you will be responsible for assisting with quality-related activities at the facility associated with incoming inspection, start-up verification, in-process verifications & checks, and sampling and inspection of finished products. Product families could include cannabis flower, cannabis oil, manufacturing infused products (lotion, capsules, vape pens/cartridges, transdermal patches), and food products (chocolate, gummies, cookies). This position will also help ensure products are being produced in a manner that meets all specifications and brand consistency. You will also assist in identifying potential quality risks and working with operations personnel to develop improvement opportunities. The ideal candidate must possess a strong attention to detail and experience working within a highly regulated industry.
CORE JOB DUTIES
- Performs incoming inspections, as needed
- Performs finished product sampling and inspection.
- Performs equipment and product line clearances before processing/production runs.
- Performs in-process verifications to ensure product weights, correct labeling & packaging for transfer.
- Performs verifications on finished product with metal detection or x-ray, as deemed necessary.
- Assists in customer complaints and product investigations, helping to assess risk, identify root cause and quarantine product.
- Inspects packaged orders to ensure correct content and quantities, as deemed necessary.
- Reviews in-process batch documentation to ensure real-time compliance to product specifications, good documentation practices and written policies/procedures.
- Monitors compliance to established Good Manufacturing Practice (GMP) guidance.
- Conducts all duties in compliance with safety rules, applicable SOPs, and other applicable guidelines.
- May require travel to other states or facilities to assist with inspections or quality issues.
REQUIRED EXPERIENCE, EDUCATION AND SKILLS
- Bachelors Degree, 1-3 years experience or Associate Degree, 5+ years experience
- Prior experience in highly regulated industry. Highly desirable: cannabis, healthcare, medical devices, pharmaceutical, consumer packaged goods (food). Highly desirable: Cannabis, FDA, HACCP, SQF experience
- Prior experience in Quality Assurance or Quality Control function
- Prior experience with product sampling, inspection procedures, customer complaints, product investigations, and CAPA desired
- Ability to follow written procedures and monitor others for adherence to written procedures
- Ability to create or update written procedures with site operations personnel, as needed
- Strong written and verbal communication skills
- Detail-oriented
- Utilizes critical thinking to troubleshoot issues, work collaboratively with a team to brainstorm solutions, and implement improvement solutions
ADDITIONAL REQUIREMENTS
- Must be 21 years of age or older to apply
- Must comply with all legal or company regulations for working in the industry
Cresco Labs is an Equal Opportunity Employer and all applicants will be considered without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status.
Apply for this job with Cresco Labs
Apply now →
By clicking the "Apply now" button, you'll be leaving Fazow and going to an external job application page for this company.
Please research all companies before applying. When applying for jobs, you should NOT have to pay to apply.
Fazow accepts no liability or responsibility as a consequence of any reliance upon information on external sites or in jobs listed on fazow.com.
Job Description
Cansortium Inc is a vertically integrated cultivator, processor, formulator, and retailer of Premium Cannabis Products currently operating in Florida, Pennsylvania and Texas as Fluent Cannabis, as well as in Michigan through its in-market partner. Our purpose is to compassionately provide patients access to the highest level of medical cannabis in an unrivaled, professional healthcare environment with outstanding customer service. Patient care always comes first at Fluent and our standards, practices, and performance is unmatched.
We are looking for leaders who want to work alongside great talent and create a positive work experience for their team. We are focused on continuous improvements, which creates development opportunities, engaged feedback, and increased contributions towards our goals as a leader in the medical cannabis industry.
Find out more at www.getfluent.com. Follow us on LinkedIn.
ROLE SUMMARY
A Quality Assurance Technician is responsible for assuring consistent production quality by developing and enforcing good manufacturing practice (GMP) systems, validating processes, performing audits, handling system improvements and providing documentation.
Hours
Wednesday
Thursday
Friday
Saturday
7:30 a - 6:30 p
7:30 a - 6:30 p
8:15 a - 7:15 p
8:15 a - 7:15 p
KEY RESPONSIBILITIES
- Assures consistent quality of production by developing and enforcing good manufacturing practice (GMP) systems, validating processes and providing documentation
- Accomplishes quality assurance human resource objectives by orienting, training, assigning, scheduling, coaching, and counseling.
- Achieves quality assurance operational objectives by contributing information and analysis to strategic plans and reviews; preparing and completing action plans; implementing production, productivity, quality, identifying and resolving problems; completing audits; determining system improvements, implementing change and initiating corrective actions.
- Develops quality assurance plans by conducting hazard analyses; identifying critical control points and preventive measures; establishing critical limits, monitoring procedures, corrective actions, and verification procedures; and monitoring inventories.
- Validates quality processes by establishing product specifications and quality attributes, measuring production, documenting evidence, determining operational and performance qualification, and writing and updating quality assurance procedures.
- Maintains and improves product quality by completing product, company, system, compliance, and surveillance audits, and investigating customer complaints.
- Collaborates with other members of management to develop new product and engineering designs, and manufacturing and training methods.
- Prepares quality documentation and reports by collecting, analyzing and summarizing information and trends including failed processes, recalls, corrective actions, and re-validations.
- Updates job knowledge by studying trends in and developments in quality management; participating in educational opportunities; reading professional publications; maintaining personal networks; participating in professional organizations.
- Enhances department and organization reputation by accepting ownership for accomplishing new and different requests; exploring opportunities to add value to job accomplishments.
QUALIFICATIONS
- Bachelor of Science degree or related field.
- Minimum two years of experience in a Quality Management/ Quality Control, supporting Pharmaceutical, Manufacturing or other regulated industry.
- GMP knowledge with a focus in operational excellence in GMPs, recalls, electronic and hard copy records in an operational environment.
- Experience with QA measuring and testing equipment
- Knowledge of safety requirements and legal standards
- Working knowledge of quality system requirements
- Experience with MS Word, Excel, Project Management, and Analytics software
- Analyzing information
- Strategic planning
- Informing others
- Emphasizing excellence
- Dealing with complexity
SKILLS
- Must be a multitasker, with the ability to work on several requests simultaneously without losing focus
- Organization and initiative, good communications skills, proactive, problem-solving, time management, discretion and confidentiality are essential attributes
- Excellent critical thinking and analytical skills
- Must possess an inquisitive and creative mind
- Ability to build good relationships. There will be frequent contact with internal, either face to face or by telephone or email
- Teamwork- collaborating with others to improve overall standards of work and service
- Thoroughness
REQUIRED EDUCATION and EXPERIENCE
- Bachelor of Science degree or related field
ADDITIONAL REQUIREMENTS
Per state law, must be at least 21 years of age.
Must successfully complete a comprehensive background check.
Must pass a drug screening
SUPERVISORY RESPONSIBILITIES
This position has no supervisory responsibilities
WORK ENVIRONMENT
This position operates in cultivation and manufacturing environments. This role routinely uses cultivation processing equipment and standard office equipment such as computers, phones, photocopiers, filing cabinets and fax machines.
PHYSICAL DEMANDS
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. While performing the duties of this job, the employee is regularly required to speak and hear. The employee frequently is required to stand for extended periods; walk; use hands to handle or feel objects, tools or controls; reach with hands and arms. Must be able to individually lift up to 25 lbs. Regular and predictable attendance is essential.
POSITION TYPE / EXPECTED HOURS OF WORK
This position regularly requires long hours and frequent weekend work.
TRAVEL
Travel is primarily local during the business day, although some out-of-the-area and overnight travel may be expected.
OTHER DUTIES
Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.
The company will ask you to help out in other departments depending on company needs. This means that you may not always work in the department that you were hired, teamwork and getting product out to patients is the goal and this means helping out where you are needed is crucial to your success as well as the company’s success.
AAP/EEO Statement
Fluent is an equal opportunity employer and we welcome applications from all backgrounds regardless of race, color, religion, sex, ancestry, age, marital status, sexual orientation, gender identity, disability or any other classification protected by law.
COMPANY BENEFITS
Fluent provides comprehensive benefits offerings to all full-time employees. Our benefits include medical, dental and vision and supplemental insurance, paid time-off program and non-matching 401k plan.
All applicants must be legally authorized to work in United States and will be required to submit proof of such eligibility.
Please note: Only shortlisted candidates will be contacted.
Apply for this job with Fluent Cannabis Care
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Fazow accepts no liability or responsibility as a consequence of any reliance upon information on external sites or in jobs listed on fazow.com.
Job Title: Quality Assurance Technician
Department: Quality Assurance
Reports to: QA Supervisor or Team Lead
FLSA Status: Regular Full-Time
Salary: Hourly
Location: Franklin Labs
Role Summary
The Quality Assurance Technician is responsible for conducting visual scans on products in effort to assure quality and safety of products intended for consumers. QA Techs will be responsible for tracking the weight of each sample and keeping track of what cultivar is currently being worked on. Additionally, QA Techs will be required to safely handle and separate any adulterated product that is found during scans.
Key Duties and Responsibilities:
- Conduct visual inspections of cannabis for organic and inorganic adulterants and defects.
- Document inspection results by completing reports and logs and inputting data into quality database.
- Keep equipment (i.e. scales, tools, etc) in good, working order.
- Maintain a safe and healthy work environment by following departmental standard operating procedures (SOPs), adhering to cGMP SOPs, and complying with legal regulations
- Maintains and ensures that proper PPE is utilized and changed out regularly, or as needed
- Provide Feedback as needed
- Performs other duties as required
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Job Title: Quality Assurance Technician
Department: Quality Assurance
Reports to: QA Supervisor or Team Lead
FLSA Status: Regular Full-Time
Salary: Hourly
Location: Tampa, FL
Role Summary
The Quality Assurance Technician is responsible for conducting visual scans on products in effort to assure quality and safety of products intended for consumers. QA Techs will be responsible for tracking the weight of each sample and keeping track of what cultivar is currently being worked on. Additionally, QA Techs will be required to safely handle and separate any adulterated product that is found during scans.
Key Duties and Responsibilities:
- Conduct visual inspections of cannabis for organic and inorganic adulterants and defects.
- Document inspection results by completing reports and logs and inputting data into quality database.
- Keep equipment (i.e. scales, tools, etc) in good, working order.
- Maintain a safe and healthy work environment by following departmental standard operating procedures (SOPs), adhering to cGMP SOPs, and complying with legal regulations
- Maintains and ensures that proper PPE is utilized and changed out regularly, or as needed
- Provide Feedback as needed
- Performs other duties as required
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COMPANY OVERVIEW
MISSION STATEMENT
Recently named one of Entrepreneur magazine's Top 100 Cannabis Leaders, Cresco Labs is one of the largest vertically-integrated multi-state cannabis operators in the United States. Cresco is built to become the most important company in the cannabis industry by combining the most strategic geographic footprint with one of the leading distribution platforms in North America. Employing a consumer-packaged goods ("CPG") approach to cannabis, Cresco's house of brands is designed to meet the needs of all consumer segments and includes some of the most recognized and trusted national brands including Cresco, Remedi and Mindy's, a line of edibles created by James Beard Award-winning chef Mindy Segal. Sunnyside*, Cresco's national dispensary brand is a wellness-focused retailer designed to build trust, education and convenience for both existing and new cannabis consumers. Recognizing that the cannabis industry is poised to become one of the leading job creators in the country, Cresco has launched the industry's first national comprehensive Social Equity and Educational Development (SEED) initiative designed to ensure that all members of society have the skills, knowledge and opportunity to work in and own businesses in the cannabis industry.
MISSION STATEMENT
At Cresco, we aim to lead the nation's cannabis industry with a focus on regulatory compliance, product consistency, and customer satisfaction. Our operations bring legitimacy to the cannabis industry by acting with the highest level of integrity, strictly adhering to regulations, and promoting the clinical efficacy of cannabis. As Cresco grows, we will operate with the same level of professionalism and precision in each new market we move in to.
JOB SUMMARY
Cresco Labs is seeking a Quality Assurance (QA) Technician to join our manufacturing team in Lincoln, Illinois. As a QA Technician, you will be responsible for assisting with quality-related activities at the facility associated with incoming inspection, start-up verification, in-process verifications & checks, and sampling and inspection of finished products. Product families could include cannabis flower, cannabis oil, manufacturing infused products (lotion, capsules, vape pens/cartridges, transdermal patches), and food products (chocolate, gummies, cookies). This position will also help ensure products are being produced in a manner that meets all specifications and brand consistency. You will also assist in identifying potential quality risks and working with operations personnel to develop improvement opportunities. The ideal candidate must possess a strong attention to detail and experience working within a highly regulated industry.
CORE JOB DUTIES
- Performs incoming inspections, as needed
- Performs finished product sampling and inspection.
- Performs equipment and product line clearances before processing/production runs.
- Performs in-process verifications to ensure product weights, correct labeling & packaging for transfer.
- Performs verifications on finished product with metal detection or x-ray, as deemed necessary.
- Assists in customer complaints and product investigations, helping to assess risk, identify root cause and quarantine product.
- Inspects packaged orders to ensure correct content and quantities, as deemed necessary.
- Reviews in-process batch documentation to ensure real-time compliance to product specifications, good documentation practices and written policies/procedures.
- Monitors compliance to established Good Manufacturing Practice (GMP) guidance.
- Conducts all duties in compliance with safety rules, applicable SOPs, and other applicable guidelines.
- May require travel to other states or facilities to assist with inspections or quality issues.
REQUIRED EXPERIENCE, EDUCATION AND SKILLS
- Bachelors Degree, 1-3 years experience or Associate Degree, 5+ years experience
- Prior experience in highly regulated industry. Highly desirable: cannabis, healthcare, medical devices, pharmaceutical, consumer packaged goods (food). Highly desirable: Cannabis, FDA, HACCP, SQF experience
- Prior experience in Quality Assurance or Quality Control function
- Prior experience with product sampling, inspection procedures, customer complaints, product investigations, and CAPA desired
- Ability to follow written procedures and monitor others for adherence to written procedures
- Ability to create or update written procedures with site operations personnel, as needed
- Strong written and verbal communication skills
- Detail-oriented
- Utilizes critical thinking to troubleshoot issues, work collaboratively with a team to brainstorm solutions, and implement improvement solutions
ADDITIONAL REQUIREMENTS
- Must be 21 years of age or older to apply
- Must comply with all legal or company regulations for working in the industry
Cresco Labs is an Equal Opportunity Employer and all applicants will be considered without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status.
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Quality Assurance Technician
Copperstate Farms - Medical Marijuana Greenhouse
3 years ago
TITLE: Quality Assurance (QA) Technician
TERMS: Days to be worked (Full Time) – Non-Exempt
GENERAL STATEMENT OF RESPONSIBILITIES: Responsibilities of QA technicians include approving standard methods and procedures related to the production, processing, packaging, labeling and storage of cannabis. QA personnel are also responsible for the approval and release of all cannabis batches prior to their sale to clients, as well as associated maintenance of complete and auditable batch records. In an effort to assure best manufacturing practices and product safety, the QA department additionally is empowered to initiate product recalls, investigate complaints related to quality, investigate quality issues within the facility, perform audits (internal and external) and assist in the training and skill development of employees in all departments.
PRINCIPAL DUTIES: Duties of this job include, but are not limited to:
· Understanding of all QA SOPs prior to their implementation;
· Keep and maintain an auditable batch record;
· Prepare, package and send promotional samples for dispensary locations;
· Prepare and send samples for third-party testing;
· Communicate with the third-party lab regarding any questions or concerns;
· Review third party lab results;
· Compile, approve and release batches for sale to clients;
· Initiate recall protocols;
· Investigate client complaints and returned product when related to the quality of the product, and initiate established corrective actions and remediation protocols;
· Work well, professionally, and effectively with fellow co-workers;
· Other duties as assigned.
QUALIFICATIONS: The QA must be a critical thinker, detail-oriented, and be able to follow state regulations and company policies. Qualified applicants will also have intermediate experience with computers and MS Office suite. Having a scientific education is recommended, but not required. Ideal candidates possess the ability to fluidly express their thoughts and ideas to fellow coworkers, managers and state inspectors.
ACCEPTABLE EDUCATION, TRAINING & EXPERIENCE:
- Must be at least 21 years of age;
- High School diploma or equivalent required;
- Previous cannabis experience required;
· Associate’s Degree in Life Sciences preferred, but not required.
PHYSICAL REQUIREMENTS:
· Requires prolonged sitting, standing, walking, bending, lifting, and use of hands.
· Frequently requires physical exertion to manually move, lift, carry, pull, or push objects or materials.
· Frequently stooping, bending, and reaching.
· Must work indoors and outdoors year-round.
· Must work in noisy and crowded environments.
· Observe, see, hear and respond to directions given with effective outcome.
· Lift 25-40 pounds from the floor to a waist-high table when necessary.
· Crouch & bend often;
· Stand for short/ high periods of time.
· Sit for short/ medium periods of time.
· Walk for short/high periods of time
· Occasionally sit on the floor or at floor level.
· Handle the responsibilities and routine stress often associated with this position;
COMMITENT & DEPENDABILITY:
· Willingness to be an integral member of a successful team;
· Dedication to provide the highest levels of service;
· Excellent attendance and reliability;
· Adherence to company policies and procedures;
· Dedicated to maintaining confidentiality in every aspect of the job.
DISCLAIMER: This is not necessarily an exhaustive list of all responsibilities, duties, skills, efforts, requirements or working conditions associated with the job. While this is intended to be an accurate reflection of the current job, management reserves the right to revise the job or to require that other or different tasks be performed as assigned
Copperstate Farms Management is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status or any other characteristic protected by law.
Job Type: Full-time
Benefits:
- Dental Insurance
- Health Insurance
- Tuition Reimbursement
- Vision Insurance
Schedule:
- Holidays
- Monday to Friday
- Overtime
- Weekends
Experience:
- Quality Assurance: 1 year (Preferred)
Education:
- High school or equivalent (Preferred)
Application Question:
- Do you meet the minumum age requirement of 21 years of age or older ?
Work Location:
- One location
Pay Frequency:
- Bi weekly or Twice monthly
This Company Describes Its Culture as:
- Detail-oriented -- quality and precision-focused
- Innovative -- innovative and risk-taking
- People-oriented -- supportive and fairness-focused
- Team-oriented -- cooperative and collaborative
Company's website:
- Copperstatefarms.com
Benefit Conditions:
- Waiting period may apply
Work Remotely:
- No
Apply for this job with Copperstate Farms - Medical Marijuana Greenhouse
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Quality Assurance Technician 1st Shift- Cultivation (Job 1656780)
Trulieve
3 years ago
Job Title: Quality Assurance Tech 1st Shift- Cultivation
Department: Quality Assurance- Cultivation
Reports to: Quality Assurance Supervisor- Cultivation
FLSA Status: Hourly
ROLE SUMMARY:
The Quality Assurance Tech-Cultivation is responsible for conducting scans on trimmed product in effort to assure quality and safety of products intended for consumers. QA Techs will be responsible for tracking the weight of each sample and keeping track of what cultivar is currently being worked on. Additionally, QA Techs will be required to safely handle and separate any adulterated product that is found during scans.
KEY DUTIES AND RESPONSIBILITIES
-
Conduct visual inspections of cannabis for organic and inorganic adulterants and defects.
- Document inspection results by completing reports and logs and inputting data into quality database.
- Keep equipment (i.e. scales, tools, etc) in good, working order.
- Maintain a safe and healthy work environment by following departmental standard operating procedures (SOPs), adhering to cGMP SOPs, and complying with legal regulations
- Maintains and ensures that proper PPE is utilized and changed out regularly, or as needed
- Provide Feedback as needed
- Performs other duties as required
SKILLS AND QUALIFICATIONS
- High School Diploma or GED
-
Detail Oriented
- Coachable and a willingness to learn
- Ability to work in a fast-paced environment
-
Ability to focus and avoid distractions
- Comfortable operating digital scales
- Basic computer knowledge
-
Basic math and reading comprehension
- Organizational skills
ADDITIONAL MINIMUM QUALIFICATIONS
Must be able to move intermittently throughout the workday. Due to the nature of our business, it is advocated that when representing Trulieve that our professionalism meets the needs of the medical patient base that we respectively serve. To uniformly align with the organization, an individual must be able to provide a level of communication that aligns respectively with the diversification of our patients which may exhibit opportunities to assess the situation and apply meaningful service. In addition, must be able to quickly identify and insert additional support where needed to deescalate situations without compromising Trulieve's objective in serving our patient base with excellent customer service.
Must be able to push, pull, move, and/or lift a minimum of 25 pounds to a minimum height of 5 feet and be able to push, pull, move, and/or carry such weight a minimum distance of 50 feet, with or without mechanical assistance.
WORK SCHEDULE:
45+ hours weekly with flexible hours depending on business needs. Must be available to work occasional evenings, weekends and holidays. 1st shift hours: 7am-4pm. 2nd shift hours: 2pm-11pm
Equal Opportunity Employer l Trulieve Supports a Drug Free Workplace
OOwIKMZhy7
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As a condition of employment, all Curio Wellness employees must comply with the State of Maryland requirements which include providing a copy of your fingerprints in the required format and consenting to an FBI Background check and Drug Screen.
MUST BE 21 YEARS OLD
Position Overview
This role is a new role designed to drive in-process quality tasks in the Manufacturing area. This role reports directly to the Manufacturing Quality Assurance Manager while collaborating with the Site Compliance Manager for continuous improvement.
Responsibilities
- Responsible for ensuring GMP Standards, MMCC Compliance, Quality policies and procedures are adhered to
- Write, update, and maintain SOP's (Standard Operating Procedures) for the Quality Assurance Program related to Manufacturing
- Collaborate with external and internal audit processes
- Responsible for departmental non-conformances and implementation of corrective action ensuring all corrective actions are documented and outstanding actions closed in timely manner
- Participate in root cause analysis for Manufacturing quality outages
- Support training for line operators to ensure process checks are accurate
- Approve standard work for cells prior to production
- 100% execution of daily tasks, projects & objectives
- Conduct and monitor testing and inspection of materials and products to ensure finished product quality
- Identify coaching and training needs to meet quality standards
- Work 1st shift with occasional overtime
- Maintains a culture of professionalism and service
- Ensures daily compliance with policies including, but not limited to, state compliance, security protocols, access protocols, dress code, and work schedules
- Complies with all HR policies including confidentiality and non-disclosure notices
- Input to Lean process improvements for the Manufacturing quality programs
- Aid in daily updates to the Gemba Quality boards
- All other duties as assigned by management
Qualifications
Required:
- High School graduate or equivalent
- Minimum 1 year of Manufacturing quality experience or related degree.
- Worked in a GMP environment.
- Ability to pass Federal background check for Cannabis
- Ability to successfully pass the drug and alcohol testing
- Self-motivated
- Coaching & development
- Analytical and data interpretation
Preferred:
- Lean experience
Supervision Exercised
- No direct supervision of associates but daily coaching and influence of the Organization to adhere to the Quality Programs.
Curio Wellness is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law.
Job Type: Full-Time
Shift: Day
Benefits: Medical, Dental, Vision, 401K, Tuition Reimbursement, Paid Time Off, Sick Leave, Holiday Pay, Life Insurance, Employee Discounts, EAP, Workplace Perks, Free Financial Advisor
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By clicking the "Apply now" button, you'll be leaving Fazow and going to an external job application page for this company.
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Fazow accepts no liability or responsibility as a consequence of any reliance upon information on external sites or in jobs listed on fazow.com.
Quality Assurance Technician
Copperstate Farms - Medical Marijuana Greenhouse
3 years ago
TITLE: Quality Assurance (QA) Technician
TERMS: Days to be worked (Full Time) – Non-Exempt
GENERAL STATEMENT OF RESPONSIBILITIES: Responsibilities of QA technicians include approving standard methods and procedures related to the production, processing, packaging, labeling and storage of cannabis. QA personnel are also responsible for the approval and release of all cannabis batches prior to their sale to clients, as well as associated maintenance of complete and auditable batch records. In an effort to assure best manufacturing practices and product safety, the QA department additionally is empowered to initiate product recalls, investigate complaints related to quality, investigate quality issues within the facility, perform audits (internal and external) and assist in the training and skill development of employees in all departments.
PRINCIPAL DUTIES: Duties of this job include, but are not limited to:
· Understanding of all QA SOPs prior to their implementation;
· Keep and maintain an auditable batch record;
· Prepare, package and send promotional samples for dispensary locations;
· Prepare and send samples for third-party testing;
· Communicate with the third-party lab regarding any questions or concerns;
· Review third party lab results;
· Compile, approve and release batches for sale to clients;
· Initiate recall protocols;
· Investigate client complaints and returned product when related to the quality of the product, and initiate established corrective actions and remediation protocols;
· Work well, professionally, and effectively with fellow co-workers;
· Other duties as assigned.
QUALIFICATIONS: The QA must be a critical thinker, detail-oriented, and be able to follow state regulations and company policies. Qualified applicants will also have intermediate experience with computers and MS Office suite. Having a scientific education is recommended, but not required. Ideal candidates possess the ability to fluidly express their thoughts and ideas to fellow coworkers, managers and state inspectors.
ACCEPTABLE EDUCATION, TRAINING & EXPERIENCE:
- Must be at least 21 years of age;
- High School diploma or equivalent required;
- Previous cannabis experience required;
· Associate’s Degree in Life Sciences preferred, but not required.
PHYSICAL REQUIREMENTS:
· Requires prolonged sitting, standing, walking, bending, lifting, and use of hands.
· Frequently requires physical exertion to manually move, lift, carry, pull, or push objects or materials.
· Frequently stooping, bending, and reaching.
· Must work indoors and outdoors year-round.
· Must work in noisy and crowded environments.
· Observe, see, hear and respond to directions given with effective outcome.
· Lift 25-40 pounds from the floor to a waist-high table when necessary.
· Crouch & bend often;
· Stand for short/ high periods of time.
· Sit for short/ medium periods of time.
· Walk for short/high periods of time
· Occasionally sit on the floor or at floor level.
· Handle the responsibilities and routine stress often associated with this position;
COMMITENT & DEPENDABILITY:
· Willingness to be an integral member of a successful team;
· Dedication to provide the highest levels of service;
· Excellent attendance and reliability;
· Adherence to company policies and procedures;
· Dedicated to maintaining confidentiality in every aspect of the job.
DISCLAIMER: This is not necessarily an exhaustive list of all responsibilities, duties, skills, efforts, requirements or working conditions associated with the job. While this is intended to be an accurate reflection of the current job, management reserves the right to revise the job or to require that other or different tasks be performed as assigned
Copperstate Farms Management is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status or any other characteristic protected by law.
Job Type: Full-time
Experience:
- Quality Assurance: 1 year (Preferred)
Education:
- High school or equivalent (Preferred)
Application Question:
- Do you meet the minumum age requirement of 21 years of age or older ?
Benefits:
- Health insurance
- Dental insurance
- Vision insurance
- Paid time off
- Professional development assistance
- Tuition reimbursement
- Other
Pay Frequency:
- Bi weekly or Twice monthly
Schedule:
- Monday to Friday
- Weekends required
- Day shift
- Overtime
Company's website:
- Copperstatefarms.com
Work Remotely:
- No
Apply for this job with Copperstate Farms - Medical Marijuana Greenhouse
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By clicking the "Apply now" button, you'll be leaving Fazow and going to an external job application page for this company.
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Fazow accepts no liability or responsibility as a consequence of any reliance upon information on external sites or in jobs listed on fazow.com.
Overview:
Are you a hardworking authority on laboratory test methods and procedures, looking to drive quality at a leading consumer packaged goods company? Do you have a degree in science along with experience in a lab environment? If so, then we have an opportunity for you!
We are currently looking for a QA Laboratory Technician at Philip Morris USA in Richmond, VA. The position will work with other laboratory staff in a team environment to deliver accurate, timely, quality test results, maintain laboratory testing equipment and provide skilled technical support. Flexibility is required to support all production shifts, weekends and holidays as needed.
What will you be doing?
What does your background and experience look like?
Company Overview:Altria Group is a FORTUNE 200 company that leads the premier tobacco companies in the United States. Headquartered in Richmond, Virginia, Altria Group holds diversified positions across tobacco, alcohol, and cannabis. Our tobacco companies include some of the most enduring names in American business: Philip Morris USA, U.S. Smokeless Tobacco Company, John Middleton, and Nat Sherman. We have 35 percent ownership of JUUL Labs, Inc., the nation’s leading e-vapor company. And we have an 80% interest in Helix Innovations, which manufactures and markets on!, an oral tobacco-derived nicotine pouch product. We complement our total tobacco business with our ownership of Ste. Michelle Wine Estates and our significant equity investment in Anheuser-Busch InBev, the world's largest brewer. Altria’s significant stake in Cronos Group, a leading global cannabinoid company, represents an exciting new global growth opportunity. At Altria, we recognize that our people are the reason we achieve our business goals. It’s only through diverse perspectives and insights that we will be able to take on the important challenges we will face to dramatically transform our business – and our industry. The work opportunities and experiences, combined with training, development, and advancement programs, allow our employees to achieve their full potential and deliver superior business results. We have the opportunity to make more progress on harm reduction in the next 10 years than we have in the past 50 years. Join us as we work together to shape a better future for adult tobacco consumers, our employees, and our shareholders. Each Altria company is an equal opportunity employer.
Are you a hardworking authority on laboratory test methods and procedures, looking to drive quality at a leading consumer packaged goods company? Do you have a degree in science along with experience in a lab environment? If so, then we have an opportunity for you!
We are currently looking for a QA Laboratory Technician at Philip Morris USA in Richmond, VA. The position will work with other laboratory staff in a team environment to deliver accurate, timely, quality test results, maintain laboratory testing equipment and provide skilled technical support. Flexibility is required to support all production shifts, weekends and holidays as needed.
What will you be doing?
- Sampling and testing raw and in-process materials for conformance to specifications and releasing approved materials to production.
- Perform testing related to process monitoring and quality control.
- Reviewing and approving data generated by the laboratory staff.
- Performing calibrations, verifications, maintenance, and troubleshooting on laboratory equipment to assure that quality system requirements are met or exceeded.
- Initiating and leading out of specification and suspect data investigations and implementing corrective and preventive actions where appropriate.
- Managing inventory of laboratory consumables, reagents, and equipment calibration schedules.
- Assisting with the design of laboratory experiments for method development, method validation, and operational process improvements for the laboratory and production environments.
- Conducting peer-to-peer training on laboratory methods and processes, new documents, document revisions, and standard methodologies.
What does your background and experience look like?
- You possess a bachelor’s degree in Chemistry, another STEM field, or you have 2+ years of experience performing analytical and physical testing.
- You have worked with physical test instruments such as analytical balance, refractometer, densitometer, viscometer, sieves, etc., and performed sensory analysis of samples from various matrices.
- You have experience operating, maintaining and troubleshooting HPLC, GC, FTIR, etc.
- You expect challenges and offer effective solutions to them
- We prefer you have Quality Management System, Laboratory Information Management System, and SAP experience.
- Excellent verbal, written, and digital literacy, including the ability to work effectively with Microsoft Excel and Word.
- Strong leadership skills and can work independently or as part of a team.
- Ability to plan, prioritize and execute work activities to ensure completion of testing requirements.
- You are willing and able to spend most of the work day standing, climbing steps, ladders, and to lift samples or equipment weighing up to 50 pounds.
Company Overview:Altria Group is a FORTUNE 200 company that leads the premier tobacco companies in the United States. Headquartered in Richmond, Virginia, Altria Group holds diversified positions across tobacco, alcohol, and cannabis. Our tobacco companies include some of the most enduring names in American business: Philip Morris USA, U.S. Smokeless Tobacco Company, John Middleton, and Nat Sherman. We have 35 percent ownership of JUUL Labs, Inc., the nation’s leading e-vapor company. And we have an 80% interest in Helix Innovations, which manufactures and markets on!, an oral tobacco-derived nicotine pouch product. We complement our total tobacco business with our ownership of Ste. Michelle Wine Estates and our significant equity investment in Anheuser-Busch InBev, the world's largest brewer. Altria’s significant stake in Cronos Group, a leading global cannabinoid company, represents an exciting new global growth opportunity. At Altria, we recognize that our people are the reason we achieve our business goals. It’s only through diverse perspectives and insights that we will be able to take on the important challenges we will face to dramatically transform our business – and our industry. The work opportunities and experiences, combined with training, development, and advancement programs, allow our employees to achieve their full potential and deliver superior business results. We have the opportunity to make more progress on harm reduction in the next 10 years than we have in the past 50 years. Join us as we work together to shape a better future for adult tobacco consumers, our employees, and our shareholders. Each Altria company is an equal opportunity employer.
Apply for this job with Altria
Apply now →
By clicking the "Apply now" button, you'll be leaving Fazow and going to an external job application page for this company.
Please research all companies before applying. When applying for jobs, you should NOT have to pay to apply.
Fazow accepts no liability or responsibility as a consequence of any reliance upon information on external sites or in jobs listed on fazow.com.
Overview
Company Overview
Altria Group is a FORTUNE 200 company that leads the premier tobacco companies in the United States. Headquartered in Richmond, Virginia, Altria Group holds diversified positions across tobacco, alcohol, and cannabis. Our tobacco companies include some of the most enduring names in American business: Philip Morris USA, U.S. Smokeless Tobacco Company, John Middleton, and Nat Sherman. We have 35 percent ownership of JUUL Labs, Inc., the nation s leading e-vapor company. And we have an 80% interest in Helix Innovations, which manufactures and markets on!, an oral tobacco-derived nicotine pouch product. We complement our total tobacco business with our ownership of Ste. Michelle Wine Estates and our significant equity investment in Anheuser-Busch InBev, the world's largest brewer. Altria s significant stake in Cronos Group, a leading global cannabinoid company, represents an exciting new global growth opportunity.
At Altria, we recognize that our people are the reason we achieve our business goals. It s only through diverse perspectives and insights that we will be able to take on the important challenges we will face to dramatically transform our business and our industry. The work opportunities and experiences, combined with training, development, and advancement programs, allow our employees to achieve their full potential and deliver superior business results. We have the opportunity to make more progress on harm reduction in the next 10 years than we have in the past 50 years. Join us as we work together to shape a better future for adult tobacco consumers, our employees, and our shareholders. Each Altria company is an equal opportunity employer.
Are you a hardworking authority on laboratory test methods and procedures, looking to drive quality at a leading consumer packaged goods company? Do you have a degree in science along with experience in a lab environment? If so, then we have an opportunity for you!
We are currently looking for a QA Laboratory Technician at Philip Morris USA in Richmond, VA. The position will work with other laboratory staff in a team environment to deliver accurate, timely, quality test results, maintain laboratory testing equipment and provide skilled technical support. Flexibility is required to support all production shifts, weekends and holidays as needed.
What will you be doing?
Sampling and testing raw and in-process materials for conformance to specifications and releasing approved materials to production.
Perform testing related to process monitoring and quality control.
Reviewing and approving data generated by the laboratory staff.
Performing calibrations, verifications, maintenance, and troubleshooting on laboratory equipment to assure that quality system requirements are met or exceeded.
Initiating and leading out of specification and suspect data investigations and implementing corrective and preventive actions where appropriate.
Managing inventory of laboratory consumables, reagents, and equipment calibration schedules.
Assisting with the design of laboratory experiments for method development, method validation, and operational process improvements for the laboratory and production environments.
Conducting peer-to-peer training on laboratory methods and processes, new documents, document revisions, and standard methodologies.
What does your background and experience look like?
You possess a bachelors degree in Chemistry, another STEM field, or you have 2+ years of experience performing analytical and physical testing.
You have worked with physical test instruments such as analytical balance, refractometer, densitometer, viscometer, sieves, etc., and performed sensory analysis of samples from various matrices.
You have experience operating, maintaining and troubleshooting HPLC, GC, FTIR, etc.
You expect challenges and offer effective solutions to them
We prefer you have Quality Management System, Laboratory Information Management System, and SAP experience.
Excellent verbal, written, and digital literacy, including the ability to work effectively with Microsoft Excel and Word.
Strong leadership skills and can work independently or as part of a team.
Ability to plan, prioritize and execute work activities to ensure completion of testing requirements.
You are willing and able to spend most of the work day standing, climbing steps, ladders, and to lift samples or equipment weighing up to 50 pounds.
Company Overview
Altria Group is a FORTUNE 200 company that leads the premier tobacco companies in the United States. Headquartered in Richmond, Virginia, Altria Group holds diversified positions across tobacco, alcohol, and cannabis. Our tobacco companies include some of the most enduring names in American business: Philip Morris USA, U.S. Smokeless Tobacco Company, John Middleton, and Nat Sherman. We have 35 percent ownership of JUUL Labs, Inc., the nation s leading e-vapor company. And we have an 80% interest in Helix Innovations, which manufactures and markets on!, an oral tobacco-derived nicotine pouch product. We complement our total tobacco business with our ownership of Ste. Michelle Wine Estates and our significant equity investment in Anheuser-Busch InBev, the world's largest brewer. Altria s significant stake in Cronos Group, a leading global cannabinoid company, represents an exciting new global growth opportunity.
At Altria, we recognize that our people are the reason we achieve our business goals. It s only through diverse perspectives and insights that we will be able to take on the important challenges we will face to dramatically transform our business and our industry. The work opportunities and experiences, combined with training, development, and advancement programs, allow our employees to achieve their full potential and deliver superior business results. We have the opportunity to make more progress on harm reduction in the next 10 years than we have in the past 50 years. Join us as we work together to shape a better future for adult tobacco consumers, our employees, and our shareholders. Each Altria company is an equal opportunity employer.
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Gage Cannabis, Co (USA) is on a mission to become the leader in the cannabis segment for Cultivation, Processing and Provisioning. We strive for the highest standards in social responsibility and ethical business practices. The company's world-class cannabis team produces indoor cannabis that is hydroponically grown in small batches with a focus on premium quality.
We are looking for a team-oriented individual who is able to work efficiently in a fast-paced environment. The successful candidate is capable of following detailed directions while demonstrating forethought and initiative to maintain a positive work environment while willing to assist other team members as needed. This position requires a blend of skills and experience that is specifically focused on both Quality and Process Control. You will provide leadership with all Quality, compliance, training and audit data and reporting.
Responsibilities include: Establishing and completing regular audits to validate the team is following SOPs and compliance related requirements. In addition, creating training programs for new employees, and regularly updating team members with any changes to SOPs or job requirements. The Cannabis industry is extremely regulated, quick and accurate information and implementation of key activities is critical in this role. This candidate must have the ability to provide feedback to team members, control and report critical information to the management team. This position will support or Provisioning centers and will require travel between facilities.
RESPONSIBILITIES
- Support all test procedures for state regulated labs
- Create and maintain facility Standard Operating Procedures
- Perform process and compliance audits to maintain a positive status with the MRA
- Establishing training programs and implementation of programs to team members
- Introduce and implement any new compliance regulations
- Responsible for facility calibration and accuracy
- Coordinate all facility related MRA communications with legal department
- Support all facility inspections, including follow-up and document control
- Monitor quality of product in and out of the facility
- Daily communication and coordination of efforts with local management
QUALIFICATIONS
- Must be 21 years or older and be able to pass a background check
- Degree in Quality Assurance/Control preferred
- 3 Years experience in Quality Assurance required
- METRC experience highly preferred
- Ability to quickly learn and master new skills
- Strong math skills, proficiency using Microsoft Excel and Word
- Previous process audit experience a plus
- Detail-oriented, dependable and able to work well both alone and with others
- Strong communication skills, both verbal and written
- Employee needs to be able to walk, sit, stand, crouch and reach throughout the day
- Ability to adapt effectively with a continually changing in a demanding environment
- Must be able to demonstrate an ability and willingness to communicate effectively in order to maintain high levels of accuracy, quality and efficiency
- Must have own reliable transportation with the ability to travel between facilities as needed
Full Time: $40-45K a year based on experience and successful interview; full benefits and growth opportunities
Gage USA is an Equal Opportunity Employer and is committed to conduct all its activities in a barrier-free and inclusive manner. We thank all candidates for their interest in Gage USA; however, only successful applicants will be contacted for an interview.
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Please research all companies before applying. When applying for jobs, you should NOT have to pay to apply.
Fazow accepts no liability or responsibility as a consequence of any reliance upon information on external sites or in jobs listed on fazow.com.
Gage Cannabis, Co (USA) is on a mission to become the leader in the cannabis segment for Cultivation, Processing and Provisioning. We strive for the highest standards in social responsibility and ethical business practices. The company's world-class cannabis team produces indoor cannabis that is hydroponically grown in small batches with a focus on premium quality.
We are looking for a team-oriented individual who is able to work efficiently in a fast-paced environment. The successful candidate is capable of following detailed directions while demonstrating forethought and initiative to maintain a positive work environment while willing to assist other team members as needed. This position requires a blend of skills and experience that is specifically focused on both Quality and Process Control. You will provide leadership with all Quality, compliance, training and audit data and reporting.
Responsibilities include: Establishing and completing regular audits to validate the team is following SOPs and compliance related requirements. In addition, creating training programs for new employees, and regularly updating team members with any changes to SOPs or job requirements. The Cannabis industry is extremely regulated, quick and accurate information and implementation of key activities is critical in this role. This candidate must have the ability to provide feedback to team members, control and report critical information to the management team.
RESPONSIBILITIES
- Support all test procedures for state regulated labs
- Create and maintain facility Standard Operating Procedures
- Perform process and compliance audits to maintain a positive status with the MRA
- Establishing training programs and implementation of programs to team members
- Introduce and implement any new compliance regulations
- Responsible for facility calibration and accuracy
- Coordinate all facility related MRA communications with legal department
- Support all facility inspections, including follow-up and document control
- Monitor quality of product in and out of the facility
- Daily communication and coordination of efforts with local management
QUALIFICATIONS
- Must be 21 years or older and be able to pass a background check
- Degree in Quality Assurance/Control preferred
- 3 Years experience in Quality Assurance required
- METRC experience highly preferred
- Ability to quickly learn and master new skills
- Strong math skills, proficiency using Microsoft Excel and Word
- Previous process audit experience a plus
- Detail-oriented, dependable and able to work well both alone and with others
- Strong communication skills, both verbal and written
- Employee needs to be able to walk, sit, stand, crouch and reach throughout the day
- Ability to adapt effectively with a continually changing in a demanding environment
- Must be able to demonstrate an ability and willingness to communicate effectively in order to maintain high levels of accuracy, quality and efficiency
Full Time: $40-45K a year based on experience and successful interview; full benefits and growth opportunities
Gage USA is an Equal Opportunity Employer and is committed to conduct all its activities in a barrier-free and inclusive manner. We thank all candidates for their interest in Gage USA; however, only successful applicants will be contacted for an interview.
Apply for this job with Gage
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By clicking the "Apply now" button, you'll be leaving Fazow and going to an external job application page for this company.
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Fazow accepts no liability or responsibility as a consequence of any reliance upon information on external sites or in jobs listed on fazow.com.
Founded in Hamilton, Ontario in 2014, Radicle Medical Marijuana is a licensed Cannabis Company under the Cannabis Act. Radicle and Gage have a mission to become the leader in the craft cannabis segment with the highest standards in social responsibility and ethical business practices and is a proud platinum member of the Ontario Living Wage Program. The company’s world-class cannabis team produces premium indoor small-batch cannabis that is hydroponically grown. Radicle/Gage received its grower’s license in January 2018.
The Quality Assurance Technician, under the direction of the Head of Quality is primarily responsible for the monitoring and quality control of cannabis production and extraction processes. The role will also be responsible for ensuring compliance with the Cannabis Act and Good Production Practices (GPP).
Job Duties
- Ensure that all standard operating procedures are being strictly followed at all times
- Ensure compliance with Cannabis Act
- Assist implement and maintain GPP
- Collaborate with other departments to ensure compliance with standard operating procedures
- Perform in-process QA inspections and ensure that all activities within production area are executed as per defined SOPs
- Adopt and incorporate quality methods into everyday work
- Maintain QA control documentation
- Identify relevant QA training needs and opportunities
- Conduct QC tests and create reports in compliance with corporate policies, practices, and procedures
- Assist with the maintenance of QA monitoring programs, including Temperature, Humidity, In-process checks, Production logs
- Conduct inspection of in-coming materials for production and ensure they are by approved by Quality before usage
- Ensure that refuse and cannabis products are managed or destroyed in accordance with Cannabis Act
- Complete inspection reports on production equipment, sanitation practices, and production areas
- Ensure that staff training is complete for SOPs and GPP
- Recommend and initiate (upon approval from the Supervisor) corrective action and change controls
- Perform any other tasks assigned by the Manager or Head of the Dept.
Core Competencies
- Planning and Organizing
- Quality Orientation
- Enforcing Rules and Regulations
- Problem Solving
- Communication
- Accountability and Dependability
- Results Orientation
- Ethics and Integrity
Professional Requirements
- At least three years of work experience in a quality assurance role in pharmaceutical, food, or related industry
- Postsecondary degree or diploma in biological science (chemistry, biology, pharmacology)
- Previous experience with extraction equipment
- Knowledge of Cannabis Act and other cannabis regulations is an asset
- Experience with an organization regulated by HACCP Canada or experience in a similarly regulated environment (GMP, GAP, GPP)
- Ability to follow strict operating procedures
- Ability to work individually as well as part of a team
- Ability to adapt to new technology
- Dedication to safety measures and best practices
- Ability to prioritize and manage conflicting demands
- Ability to effectively communicate both verbally and in writing
- High level of integrity and work ethic
Please send your resume and cover letter to [email protected]. We thank all applicants for their interest but only those selected for an interview will be contacted.
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Curaleaf Holdings, Inc. (CSE: CURA) (OTCQX: CURLF) ("Curaleaf") is a leading vertically integrated multi-state cannabis operator with a dominant presence on both the East and West coasts of the United States, the largest cannabis market in the world. As a high-growth cannabis company known for quality, expertise, and reliability, the company and its brands, Curaleaf and Select, provide industry-leading service, product selection, and accessibility across the medical and adult-use markets. Strategically positioned in highly populated, limited-license states, the company currently operates in 14 states with 53 dispensaries, 15 cultivation sites, and 24 processing sites. Following the Select closing, Curaleaf will employ over 2,200 people across the United States.
Summary Compiles and verifies inventory records and confirms product quality requirements are met by performing the following duties.
Essential Duties and Responsibilities include the following. Other duties may be assigned.
Competencies
The ability to speak, read/write in English, basic math skills, and practical experience using computer software like Microsoft Office, are essential for success in this role. The candidate must exhibit the behaviors below and must be able to perform each essential duty satisfactorily after a reasonable amount of training.
Can do attitude- Focuses on solving problems, not blaming; Listens to others without interrupting; Keeps emotions under control; Remains open to others' ideas and tries new things.
Team Player – Balances individual responsibilities; Gives and welcomes feedback; Contributes to building a positive team spirit; Puts success of team above own interests; Supports everyone's efforts to succeed.
Ethical - Treats people with respect; Keeps commitments; Works with integrity and ethically; Upholds organizational values.
Safety and Security focused - Observes safety and security procedures; Reports potentially unsafe conditions; Uses equipment and materials properly.
Education and/or Experience
One-year certificate from college or technical school; or three to six months related experience and/or training; or equivalent combination of education and experience.
Summary Compiles and verifies inventory records and confirms product quality requirements are met by performing the following duties.
Essential Duties and Responsibilities include the following. Other duties may be assigned.
- Conducts inventory inspections to monitor and ensure traceability of plant/product movement throughout the facility.
- Performs or assists in quality control inspections as directed to confirm established product quality requirements have been achieved.
- Promptly communicates identified discrepancies to team leads, and documents accordingly. Investigates & participates in correction activities as directed.
- Accurately completes documentation & enters data to ensure compliance with internal and regulatory requirements.
- Maintains strict adherence to established procedures.
- Participates in problem solving activities to drive process improvements.
Competencies
The ability to speak, read/write in English, basic math skills, and practical experience using computer software like Microsoft Office, are essential for success in this role. The candidate must exhibit the behaviors below and must be able to perform each essential duty satisfactorily after a reasonable amount of training.
Can do attitude- Focuses on solving problems, not blaming; Listens to others without interrupting; Keeps emotions under control; Remains open to others' ideas and tries new things.
Team Player – Balances individual responsibilities; Gives and welcomes feedback; Contributes to building a positive team spirit; Puts success of team above own interests; Supports everyone's efforts to succeed.
Ethical - Treats people with respect; Keeps commitments; Works with integrity and ethically; Upholds organizational values.
Safety and Security focused - Observes safety and security procedures; Reports potentially unsafe conditions; Uses equipment and materials properly.
Education and/or Experience
One-year certificate from college or technical school; or three to six months related experience and/or training; or equivalent combination of education and experience.
Apply for this job with Curaleaf
Apply now →
By clicking the "Apply now" button, you'll be leaving Fazow and going to an external job application page for this company.
Please research all companies before applying. When applying for jobs, you should NOT have to pay to apply.
Fazow accepts no liability or responsibility as a consequence of any reliance upon information on external sites or in jobs listed on fazow.com.
Curaleaf Holdings, Inc. (CSE: CURA) (OTCQX: CURLF) ("Curaleaf") is a leading vertically integrated multi-state cannabis operator with a dominant presence on both the East and West coasts of the United States, the largest cannabis market in the world. As a high-growth cannabis company known for quality, expertise, and reliability, the company and its brands, Curaleaf and Select, provide industry-leading service, product selection, and accessibility across the medical and adult-use markets. Strategically positioned in highly populated, limited-license states, the company currently operates in 14 states with 53 dispensaries, 15 cultivation sites, and 24 processing sites. Following the Select closing, Curaleaf will employ over 2,200 people across the United States.
Summary Compiles and verifies inventory records and confirms product quality requirements are met by performing the following duties.
Essential Duties and Responsibilities include the following. Other duties may be assigned.
Competencies
The ability to speak, read/write in English, basic math skills, and practical experience using computer software like Microsoft Office, are essential for success in this role. The candidate must exhibit the behaviors below and must be able to perform each essential duty satisfactorily after a reasonable amount of training.
Can do attitude- Focuses on solving problems, not blaming; Listens to others without interrupting; Keeps emotions under control; Remains open to others' ideas and tries new things.
Team Player – Balances individual responsibilities; Gives and welcomes feedback; Contributes to building a positive team spirit; Puts success of team above own interests; Supports everyone's efforts to succeed.
Ethical - Treats people with respect; Keeps commitments; Works with integrity and ethically; Upholds organizational values.
Safety and Security focused - Observes safety and security procedures; Reports potentially unsafe conditions; Uses equipment and materials properly.
Education and/or Experience
One-year certificate from college or technical school; or three to six months related experience and/or training; or equivalent combination of education and experience.
Summary Compiles and verifies inventory records and confirms product quality requirements are met by performing the following duties.
Essential Duties and Responsibilities include the following. Other duties may be assigned.
- Conducts inventory inspections to monitor and ensure traceability of plant/product movement throughout the facility.
- Performs or assists in quality control inspections as directed to confirm established product quality requirements have been achieved.
- Promptly communicates identified discrepancies to team leads, and documents accordingly. Investigates & participates in correction activities as directed.
- Accurately completes documentation & enters data to ensure compliance with internal and regulatory requirements.
- Maintains strict adherence to established procedures.
- Participates in problem solving activities to drive process improvements.
Competencies
The ability to speak, read/write in English, basic math skills, and practical experience using computer software like Microsoft Office, are essential for success in this role. The candidate must exhibit the behaviors below and must be able to perform each essential duty satisfactorily after a reasonable amount of training.
Can do attitude- Focuses on solving problems, not blaming; Listens to others without interrupting; Keeps emotions under control; Remains open to others' ideas and tries new things.
Team Player – Balances individual responsibilities; Gives and welcomes feedback; Contributes to building a positive team spirit; Puts success of team above own interests; Supports everyone's efforts to succeed.
Ethical - Treats people with respect; Keeps commitments; Works with integrity and ethically; Upholds organizational values.
Safety and Security focused - Observes safety and security procedures; Reports potentially unsafe conditions; Uses equipment and materials properly.
Education and/or Experience
One-year certificate from college or technical school; or three to six months related experience and/or training; or equivalent combination of education and experience.
Apply for this job with Curaleaf
Apply now →
By clicking the "Apply now" button, you'll be leaving Fazow and going to an external job application page for this company.
Please research all companies before applying. When applying for jobs, you should NOT have to pay to apply.
Fazow accepts no liability or responsibility as a consequence of any reliance upon information on external sites or in jobs listed on fazow.com.
Who we are
MCR Labs is an independent and accredited cannabis testing and analytics laboratory founded in 2013.
We are a passionate team of researchers, analytical chemists, pharmaceutical scientists, technologists, and cannabis enthusiasts working to advance the cannabis industry by helping providers ensure the safety and effectiveness of their products.
We are committed to proving the best possible services to our clients, building relationships and supporting our community.
This is an exceptional career opportunity to join a fast-paced, high growth company in the fastest growing industry in the world!
Job SummaryThe Quality Assurance Technician will be responsible for maintaining traceability of equipment and reagents utilizedwithin the laboratory.Duties and Responsibilitiesï‚· Conduct routine equipment calibration verificationsï‚· Inspect environment conditions within the labï‚· Ensure equipment calibration schedule is maintainedï‚· Review maintain and organize records for complianceï‚· Review traceability records for accuracy and completenessï‚· Oversee chemical reagent inventoryï‚· Work with QA team to ensure lab supplies are procured from approved vendorsï‚· Always maintain safe work practicesï‚· Follow company security and safety requirementsQualificationï‚· Education: Minimum associate degree in related field or equivalent work experience;ï‚· 1 year minimum experience working in a laboratoryï‚· Experience handling and utilizing laboratory instruments, e.g. balances, pipettes, thermometers;Requirementsï‚· Must be at least 21 years of age;ï‚· Must pass a background check;ï‚· Outstanding communication skills;ï‚· Candidate should be a self-motivator;ï‚· Outstanding observation skills;ï‚· Ability to lift 50lbs;
MCR Labs is an equal opportunity employer and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, genetic information, veteran status, or disability status.
All qualified applicants must be able to satisfy the Department of Homeland Security Form I-9 requirement, with the documents necessary to verify identity & employment authorization.
Our team is reviewing all applications as they are received. Unfortunately, we are not able to respond directly to all applicants, and we will reach out if you meet the requirements of the position for which you applied.
Job Type: Full-time
Experience:
- Laboratory: 2 years (Required)
- Quality Assurance: 2 years (Required)
Benefits:
- Health insurance
- Dental insurance
- Vision insurance
- Retirement plan
- Paid time off
Apply for this job with MCR labs
Apply now →
By clicking the "Apply now" button, you'll be leaving Fazow and going to an external job application page for this company.
Please research all companies before applying. When applying for jobs, you should NOT have to pay to apply.
Fazow accepts no liability or responsibility as a consequence of any reliance upon information on external sites or in jobs listed on fazow.com.
Curaleaf is a leading vertically integrated medical and wellness cannabis operator in the United States, Curaleaf Holdings, Inc., (CSE: CURA) (OTCQX: CURLF). It is a high-growth cannabis company with a national brand known for quality, trust, and reliability. The company is positioned in highly populated, limited license states, and currently operates in 12 states with 52 dispensaries, 14 cultivation sites and 14 processing sites. Curaleaf has the executive expertise and research and development capabilities to provide leading service, selection, and accessibility across the medical and adult-use markets, as well as the standalone CBD category.
Summary Compiles and verifies inventory records and confirms product quality requirements are met by performing the following duties.
Essential Duties and Responsibilities include the following. Other duties may be assigned.
Competencies
The ability to speak, read/write in English, basic math skills, and practical experience using computer software like Microsoft Office, are essential for success in this role. The candidate must exhibit the behaviors below and must be able to perform each essential duty satisfactorily after a reasonable amount of training.
Can do attitude- Focuses on solving problems, not blaming; Listens to others without interrupting; Keeps emotions under control; Remains open to others' ideas and tries new things.
Team Player – Balances individual responsibilities; Gives and welcomes feedback; Contributes to building a positive team spirit; Puts success of team above own interests; Supports everyone's efforts to succeed.
Ethical - Treats people with respect; Keeps commitments; Works with integrity and ethically; Upholds organizational values.
Safety and Security focused - Observes safety and security procedures; Reports potentially unsafe conditions; Uses equipment and materials properly.
Education and/or Experience
One-year certificate from college or technical school; or three to six months related experience and/or training; or equivalent combination of education and experience.
Summary Compiles and verifies inventory records and confirms product quality requirements are met by performing the following duties.
Essential Duties and Responsibilities include the following. Other duties may be assigned.
- Conducts inventory inspections to monitor and ensure traceability of plant/product movement throughout the facility.
- Performs or assists in quality control inspections as directed to confirm established product quality requirements have been achieved.
- Promptly communicates identified discrepancies to team leads, and documents accordingly. Investigates & participates in correction activities as directed.
- Accurately completes documentation & enters data to ensure compliance with internal and regulatory requirements.
- Maintains strict adherence to established procedures.
- Participates in problem solving activities to drive process improvements.
Competencies
The ability to speak, read/write in English, basic math skills, and practical experience using computer software like Microsoft Office, are essential for success in this role. The candidate must exhibit the behaviors below and must be able to perform each essential duty satisfactorily after a reasonable amount of training.
Can do attitude- Focuses on solving problems, not blaming; Listens to others without interrupting; Keeps emotions under control; Remains open to others' ideas and tries new things.
Team Player – Balances individual responsibilities; Gives and welcomes feedback; Contributes to building a positive team spirit; Puts success of team above own interests; Supports everyone's efforts to succeed.
Ethical - Treats people with respect; Keeps commitments; Works with integrity and ethically; Upholds organizational values.
Safety and Security focused - Observes safety and security procedures; Reports potentially unsafe conditions; Uses equipment and materials properly.
Education and/or Experience
One-year certificate from college or technical school; or three to six months related experience and/or training; or equivalent combination of education and experience.
Apply for this job with Curaleaf
Apply now →
By clicking the "Apply now" button, you'll be leaving Fazow and going to an external job application page for this company.
Please research all companies before applying. When applying for jobs, you should NOT have to pay to apply.
Fazow accepts no liability or responsibility as a consequence of any reliance upon information on external sites or in jobs listed on fazow.com.