Here are 19 cannabis jobs mentioning "qa manager" in April 2024, at companies like Cresco Labs, INSA, Advanced Analytics Lab LLC., and Anresco, Inc., including positions such as QA Manager, Quality Assurance (QA) Manager, Medical Cannabis Compliance Testing - Laboratory QA/QC Manager, and CI-QA MANAGER.
More than 30+ days
JOB SUMMARY
The CI/QA Manager is responsible for driving lean manufacturing practices throughout the facility along with monitoring and evaluating internal production processes, overseeing quality-related activities at the facility associated with sampling and inspection of in-process and finished products, customer complaints, product investigations, and Corrective and Prevention Action (CAPA) plans. The CI/QA manager is also responsible for development of visual processes, daily tiered production reviews, GEMA walks, focused improvement activities, safety performance, TEPM, TPS and ensuring products are being produced in a manner that meets all specifications and brand consistency and promoting a culture of Quality across all departments.
PRIMARY RESPONSIBILITES
- Identify and deliver service improvement activity across the business through employing process improvement methodologies and the application of innovative thinking
- Work with key business stakeholders, and multi-functional areas, to build a continuous improvement environment supporting a culture of change
- Lead and facilitate LEAN and process improvement-based workshops to drive ideas and solutions
- Support the delivery of greater efficiency through the identification and elimination of unnecessary complexity within business processes and identification of better ways of working
- Identify trends and process variations as part of establishing a continuous improvement monitoring system
- Assist in the development and implementation of a 'best-in-class continuous improvement strategy
- Take ownership of change initiatives from evolution/efficiency identification through to project delivery via internal governance and controls
- Work with other team members and business services departments to devise new support material based on the revised processes, to include training, reporting and systems enhancements
- Actively monitor project risks to foresee/identify potential problems and proactively identify solutions to address in advance
- Facilitate a program, deliver coaching, run projects, and document all improvements
- Complete post implementation reviews to ensure successful delivery has been achieved and to ensure that improvements can be made for future projects
- Work with the facility leadership on developing priorities and schedules
- Responsible for developing product quality safety and sanitation programs for the cultivation site.
- Build a documented consumer complaint process complete with trending, weekly reviews, and trend reduction.
- Create guidance in regulations consistent with FSMA, CGMP and food CFR requirements.
- Assurance of sound raw and FG traceability program.
- Development of Master Sanitation program.
- Implementation of thorough line quality measurement systems.
- Documentation and control of all processes.
- Lead a strong pest control program.
- Developing quality control processes.
- Observing staff and monitoring production standards.
- Examining the quality of raw/pack materials that are used in production.
- Evaluating the final output of products to determine their quality.
- Producing statistical reports on quality standards.
- Rejecting products that fail quality standards.
- Implement HACCP program all within the food work streams.
- Implement "Hold" or "Quarantine" process & tracking for product not approved for sale
JOB REQUIREMENTS
- 2-year degree in Business Administration, or relevant field. 4-year degree preferred.
- Quality Control Certification preferred.
- Minimum 3 - 5 years as a Site Quality Manager; strong food experience is a plus
- Minimum 2 years Continuous Improvement
- Experience in TPM Production Management & Operating System
- Experience with VSM (value stream management) process
- Ability to look at each situation with an open mind / Thinking outside the box
- Ability to build and manage external auditing such as SQF or BRC initiatives.
- Lean manufacturing experience and HACCP certified
- Advanced CAPA, RCA, and strategic planning experience
- Advanced experience conducting audits, data analysis and reporting statistics.
- Highly computer literate and proficient in MS Office including Excel, PowerPoint, Word and data analytics.
- Excellent critical thinking and problem-solving skills.
- Excellent interpersonal and communication skills including speaking and writing.
- Proven track record in people leadership (supporting, developing, engaging) with demonstrated teambuilding and collaboration skills.
- Facilitation of Daily Management Process & Focused Improvement Process
- Must be at least 21 years of age.
- Must pass any and all required background checks.
- Must be able to obtain and retain a Registered Agent Card issued by the state of operation
- Must be and remain compliant with any and all regulatory requirements for working in the cannabis industry.
- Must have excellent organization and time management skills.
- Must be focused, pay close attention to detail and accuracy of data recorded.
- Must be able to internalize training and follow instructions consistently.
- Must be able to communicate clearly and effectively
- Must be able to work effectively as part of a team and grow with the company
- Positive attitude, team player and strong work ethic
- Willing to build understanding of applicable state and local laws and regulations as they pertain to the industry, personnel law, safety regulations, local municipal codes and organizational rules, regulations, directives, and standard operating procedures
- Other duties and responsibilities as assigned
EEO STATEMENT
Ascend Wellness Holdings, LLC and its subsidiaries is an equal opportunity employer and celebrate the population of differences and does not discriminate in its hiring / hiring practices, regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, or any other characteristic protected by law.
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Want to work in a dispensary that values its employees as muchas its patients? Does a supportive and inclusive environment driven by feedbackand opportunity for development and growth appeal to you? Come join us at InsaCannabis, where we're in the business of making your day better! Here at Insawe create the best possible patient experience through authenticity and aredriven by a true passion for what we do. Our culture stems from our coreconcept: “We sell cannabis for real life”. We will always have an open heartand mind to all. Insa is the result of two childhood friends simply wanting tobring cannabis to real people and we're looking for people to help realize thatvision in the state of Florida!
We offer a generous vacation andsick pay package and Company-sponsored health, dental, and vision plans, inaddition to other insurance options. We also offer 401K with generous companymatch as well as fun perks such as employee discounts and free swag.
Position Summary:
We are seeking an experienced Quality Assurance (QA) Manager to oversee our quality assurance program. The QA Manager will oversee the activity of the quality assurance and analytical laboratory departments and staff, developing, implementing, and maintaining a system of quality and reliability for the organization’s products and/or development process. You will collaborate with other department heads to implement changes to increase efficiency while still maintaining high levels of quality. Your primary goal will be to ensure all our products meet OMMU regulations and safety guidelines.
Essential Functions:
- Analyze current quality assessment techniques for inconsistencies and redundancy
- Collaborates with management to achieve most efficient and accurate quality assessments
- Creates and implements a GMP (Good Manufacturing Practices) module
- Creates and Implements an SSOP (Sanitation Standard Operating Procedures)
- Creates and modifies Standard Operating Procedures according to state regulations and production needs
- Follow products through the entirety of process to ensure each step is completed correctly
- Perform detailed inspections of cannabis products and confirm they are up to standards
- Track, record, and maintain quality assurance data
- Analyze results and schedule compliance audits and exterior sampling procedures
Qualifications:
- Bachelor’s degree required
- 3-5 years of experience as a department manager in a or manufacturing-based environment required
- Proficient in Windows 10 operating system, Microsoft Office
- Experience in Lean/Six Sigma work environment a plus
- Willing and able to work a flexible schedule with some weekend work and occasional travel
- Strong people management skills required
- Ability to communicate ideas and resolutions in a clear, concise, friendly manner
- Strong written and verbal communication skills
- Demonstrated ability to effectively multi-task and manage time both independently as well as within a team environment
- Continuous Process Improvement mindset
- Must be at least 21 years of age
- Must have a reliable personal vehicle
- Must be able to pass a background check in accordance with state regulations
Physical Requirements:
- Ability to sit, stand, and walk as needed
- Ability to bend at the waist, kneel, crouch to access equipment
- Ability to lift and carry up to 50lbs
- Close visual acuity needed for viewing screens and fine print
Workplace Environment
- Consistent moderate background noise level due to HVAC and machinery
- Exposure to cannabis odor
- Exposure to skin contact with plants, to which some individuals may be allergic
Apply for this job with INSA
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.
Medical Cannabis Compliance Testing - Laboratory QA/QC Manager
Advanced Analytics Lab LLC.
About us
Advanced Analytics Lab LLC. is a small locally owned business in Fort Gibson, Oklahoma. We are collaborative, professional and data-driven.
Our work environment includes:
- Lively atmosphere
- Growth opportunities
- Relaxed atmosphere
- Casual work attire
- Flexible working hours
- Safe work environment
- Company perks
QA/QC Manager:
We are looking for a reliable Manager of Quality Assurance to ensure that all external and internal requirements are met before our product reaches our customers. You will be responsible for inspecting procedures and outputs and identifying mistakes or non-conformity issues. An excellent Quality Assurance Manager has eyes like a hawk and solid experience in quality control. The ideal candidate is a reliable and competent professional whose approval will be necessary for the continuation of a business life cycle. The goal is to assure the high quality of our operations and services aiming to the long-term success of our business.
Minimum Requirements:
- Education Required: BA or BS Degree in Related Science
- Experience Required: 2 years in a laboratory environment.
The QA/QC Manager is responsible for the following:
- The quality manager manages all aspects of quality in the lab as they pertain to the Quality Management System, Quality Manual, supporting documentation, SOPs, training of staff, and review of data.
- Be trained and proficient at each test method in the lab to enable evaluation of data objectively and perform assessments without influence.
- Have training and / or experience in QA/QC procedures and be knowledgeable in the ISO/IEC 17025.
- Ensures that the Quality Management System is established, implemented, and maintained in accordance with the ISO/IEC 17025:2017 and Oklahoma Medical Marijuana Authority.
- Have knowledge and expertise in the analytical test methods for which data review is to be performed.
- Manage the internal audit and data integrity program. Ensure full annual audits are completed.
- Notify laboratory management of deficiencies and performance of the quality system and be able to monitor corrective action.
- Review and revise SOP’s as needed in conjunction with laboratory analysts and laboratory management.
- Ensure training is being performed as needed and that the documentation is kept.
- Ensure that MDL's/LODS, IDOCs and DOCS are completed and calculated on a required frequency and that documentation is complete.
- Ensure daily method QC checks are being performed and that out-of-control situations are documented and corrected.
- Responsible for maintaining and updating the Quality Manual
- Make sure all testing personnel have the training and resources needed to complete the required testing
- Coordinate laboratory accreditation activities.
- Responsible for training all personnel on the Quality Management System and SOPs.
- Deputy to the following positions: In absence of one of the other positions the Quality Manger is responsible for the following positions: Laboratory Director, Senior Analyst, Analyst.
Job Types: Full-time, Contract
Pay: From $55,000.00 per year
Benefits:
- Dental insurance
- Flexible schedule
- Health insurance
- Paid time off
- Vision insurance
Schedule:
- 8 hour shift
- Day shift
- Monday to Friday
Supplemental Pay:
- Bonus pay
Ability to commute/relocate:
- Fort Gibson, OK 74434: Reliably commute or planning to relocate before starting work (Preferred)
Education:
- Bachelor's (Required)
Experience:
- ISO 17025: 1 year (Required)
- Analytical Cannabis Compliance Testing: 1 year (Required)
- Cannabis Laboratory QA/QC Management: 1 year (Preferred)
Shift availability:
- Day Shift (Preferred)
Work Location: One location
Apply for this job with Advanced Analytics Lab 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.
Want to work in a dispensary that values its employees as muchas its patients? Does a supportive and inclusive environment driven by feedbackand opportunity for development and growth appeal to you? Come join us at InsaCannabis, where we're in the business of making your day better! Here at Insawe create the best possible patient experience through authenticity and aredriven by a true passion for what we do. Our culture stems from our coreconcept: “We sell cannabis for real life”. We will always have an open heartand mind to all. Insa is the result of two childhood friends simply wanting tobring cannabis to real people and we're looking for people to help realize thatvision in the state of Florida!
We offer a generous vacation andsick pay package and Company-sponsored health, dental, and vision plans, inaddition to other insurance options. We also offer 401K with generous companymatch as well as fun perks such as employee discounts and free swag.
Position Summary:
We are seeking an experienced Quality Assurance (QA) Manager to oversee our quality assurance program. The QA Manager will oversee the activity of the quality assurance and analytical laboratory departments and staff, developing, implementing, and maintaining a system of quality and reliability for the organization’s products and/or development process. You will collaborate with other department heads to implement changes to increase efficiency while still maintaining high levels of quality. Your primary goal will be to ensure all our products meet OMMU regulations and safety guidelines.
Essential Functions:
- Analyze current quality assessment techniques for inconsistencies and redundancy
- Collaborates with management to achieve most efficient and accurate quality assessments
- Creates and implements a GMP (Good Manufacturing Practices) module
- Creates and Implements an SSOP (Sanitation Standard Operating Procedures)
- Creates and modifies Standard Operating Procedures according to state regulations and production needs
- Follow products through the entirety of process to ensure each step is completed correctly
- Perform detailed inspections of cannabis products and confirm they are up to standards
- Track, record, and maintain quality assurance data
- Analyze results and schedule compliance audits and exterior sampling procedures
Qualifications:
- Bachelor’s degree required
- 3-5 years of experience as a department manager in a or manufacturing-based environment required
- Proficient in Windows 10 operating system, Microsoft Office
- Experience in Lean/Six Sigma work environment a plus
- Willing and able to work a flexible schedule with some weekend work and occasional travel
- Strong people management skills required
- Ability to communicate ideas and resolutions in a clear, concise, friendly manner
- Strong written and verbal communication skills
- Demonstrated ability to effectively multi-task and manage time both independently as well as within a team environment
- Continuous Process Improvement mindset
- Must be at least 21 years of age
- Must have a reliable personal vehicle
- Must be able to pass a background check in accordance with state regulations
Physical Requirements:
- Ability to sit, stand, and walk as needed
- Ability to bend at the waist, kneel, crouch to access equipment
- Ability to lift and carry up to 50lbs
- Close visual acuity needed for viewing screens and fine print
Workplace Environment
- Consistent moderate background noise level due to HVAC and machinery
- Exposure to cannabis odor
- Exposure to skin contact with plants, to which some individuals may be allergic
Apply for this job with INSA
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.
Position Summary:
We are seeking an experienced Quality Assurance (QA) Manager to oversee our quality assurance program. The QA Manager will oversee the activity of the quality assurance and analytical laboratory departments and staff, developing, implementing, and maintaining a system of quality and reliability for the organization’s products and/or development process. You will collaborate with other department heads to implement changes to increase efficiency while still maintaining high levels of quality. Your primary goal will be to ensure all our products meet OMMU regulations and safety guidelines.
Essential Functions:
- Analyze current quality assessment techniques for inconsistencies and redundancy
- Collaborates with management to achieve most efficient and accurate quality assessments
- Creates and implements a GMP (Good Manufacturing Practices) module
- Creates and Implements an SSOP (Sanitation Standard Operating Procedures)
- Creates and modifies Standard Operating Procedures according to state regulations and production needs
- Follow products through the entirety of process to ensure each step is completed correctly
- Perform detailed inspections of cannabis products and confirm they are up to standards
- Track, record, and maintain quality assurance data
- Analyze results and schedule compliance audits and exterior sampling procedures
Qualifications:
- Bachelor’s degree required
- 3-5 years of experience as a department manager in a or manufacturing-based environment required
- Proficient in Windows 10 operating system, Microsoft Office
- Experience in Lean/Six Sigma work environment a plus
- Willing and able to work a flexible schedule with some weekend work and occasional travel
- Strong people management skills required
- Ability to communicate ideas and resolutions in a clear, concise, friendly manner
- Strong written and verbal communication skills
- Demonstrated ability to effectively multi-task and manage time both independently as well as within a team environment
- Continuous Process Improvement mindset
- Must be at least 21 years of age
- Must have a reliable personal vehicle
- Must be able to pass a background check in accordance with state regulations
Physical Requirements:
- Ability to sit, stand, and walk as needed
- Ability to bend at the waist, kneel, crouch to access equipment
- Ability to lift and carry up to 50lbs
- Close visual acuity needed for viewing screens and fine print
Workplace Environment
- Consistent moderate background noise level due to HVAC and machinery
- Exposure to cannabis odor
- Exposure to skin contact with plants, to which some individuals may be allergic
Apply for this job with INSA
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 Quality Manager to join our manufacturing facility in Mendota, CA. The Quality Manager position will report directly into the Regional Site Quality Director – West Coast. As a Quality Manager, you will be responsible for overseeing quality-related activities at the facility associated with sampling and inspection of in-process and finished products, customer complaints, product investigations, and Corrective and Preventive Action (CAPA) plans. Product families include cannabis oil, vape pens/cartridges, infused products and concentrates. This position will be responsible for ensuring products are being produced in a manner that meets all specifications and brand consistency and promoting a culture of Quality across all departments. You will also lead efforts to identify 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.
- Responsible for management of all quality related activities as the site.
- Intricate part of the site Leadership Team.
- Performs incoming packaging component, raw material, bulk material, in-process and finished product sampling and inspection.
- Performs and ensures equipment and product line clearances before production runs.
- Performs cleaning and sanitation verification.
- Performs and ensures scale and thermometer verification
- Manages and writes customer complaint and product investigations, helping to assess risk, identify root cause, plan CAPA activities, and implement solutions with business partners.
- Assist with Quality Systems document writing and revisions, including routing and/or approval of change request packages.
- Inspects and verifies compliance labels for finished goods.
- Reviews COAs for regulatory compliance and specification adherence.
- Inspects packaged orders to ensure correct content and quantities, as deemed necessary.
- Inspects retain samples and customer return samples, as deemed necessary.
- Manage and track stability sampling and testing per state regulation.
- Reviews batch manufacturing records, logbooks, test results, and ensures good documentation practices are followed.
- Discusses issues and concerns directly with line personnel and operations management so any corrections and improvements can be made in a timely manner.
- Performs GMP facility inspections.
- Participates in corporate Quality internal audits as assigned.
- Collaborates with operational functions to troubleshoot manufacturing and production defects, CAPA, and customer complaints. Provides advice with process improvements to eliminate errors and reduce risk.
- Monitors compliance to established Good Manufacturing Practice (GMP) and GFSI (Global Food Safety Initiative) guidance such as BRC, SQF, and FSSC 22000
- Facilitates creation of and/or updates to product safety plans or product process parameters.
- Overall accountability for product discontinuation, quarantine, destruction, rework, withdrawal/recall to operations and quality management.
- Perform batch record review and release of batches/lots.
- Performs data analysis and reporting including but not limited to KPIs, potency, microbiological results, and pesticide results.
- Leads mock recalls/withdrawals.
- Conducts all duties in compliance with safety rules, applicable SOPs, and other applicable guidelines.
- 5-10% travel to other facilities and states to help with new market launches, training, etc.
REQUIRED EXPERIENCE, EDUCATION AND SKILLS
- Bachelor's Degree, 5+ years experience in a quality role
- Prior experience in highly regulated industry: healthcare, medical devices, pharmaceutical, consumer packaged goods (food), cannabis, agricultural or tobacco.
- Highly desirable: FDA, HACCP, GFSI (Global Food Safety Initiative) such as BRC, SQF, and FSSC 22000
- Prior experience in Quality Assurance or Quality Control function.
- Prior experience with product sampling, inspection procedures, customer complaints, product investigations, and CAPA
- Prior experience in regulatory agency audits and correspondence.
- 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, including writing executive summaries and communicating with senior level operations, quality management team, and regulatory agencies.
- Detail-oriented
- Utilizes critical thinking to troubleshoot issues, work collaboratively with a team to brainstorm solutions, and implement improvement solutions
- Able to manage personnel effectively, including performance issues, setting vision, priorities, etc.
- Demonstrates high sense of urgency and proactive thinking.
- Experience with Continuous Improvement initiatives is a plus.
- Experience with Good Agricultural Practice (GAP) is a plus.
- Experience with Regulatory Agency Investigations is a plus
- Experience with leading Analytical Laboratories (chemical, microbiology) is a plus
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
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Pree Laboratories is hiring a Quality Assurance Manager!
About PREE:
Located in the heart of the Willamette Valley, PREE Laboratory is an OLCC licensed and ORELAP accredited high complexity environmental laboratory currently providing cannabis and hemp compliance and R&D testing solutions for our amazing clients. PREE Laboratory prides itself in providing our client-partners with the highest quality technical support and customer service in a prompt and professional manner.
This full time position is anticipated to work 9:00-5:00 Monday-Friday.
Position Description:
We are looking for a reliable QA Manger to ensure that all external and internal requirements are met before our product reaches our customers. You will be responsible for inspecting procedures and outputs and identifying mistakes or non-conformity issues. An excellent QA Manager has eyes like a hawk and solid experience in quality control. The ideal candidate is a reliable and competent professional whose approval will be necessary for the continuation of a business life cycle.
The QA Manager is responsible for the oversight and review of quality control data but is independent from laboratory operations. The QA Manager's training and proof of experience in QA/QC procedures, knowledge of analytical methods, and familiarity with the laboratory's management system is vital to the success of the laboratory. The QA Manager must have a bachelor's degree in science and experience in an environmental lab setting.
Specific Duties & Responsibilities
- Develop and update standard operating procedures to inspect and report quality issues in conjunction with laboratory director and manager
- Monitor all operations that affect quality
- Supervise and train technicians and other staff
- Assure the reliability and consistency of production by checking processes and final output
- Appraise customers’ requirements and make sure they are satisfied
- Report all malfunctions to production executives to ensure immediate action
- Facilitate proactive solutions by collecting and analyzing quality data
- Review current standards and policies
- Keep records of quality reports, statistical reviews and relevant documentation
- Ensure all legal standards are met
- Communicate with external quality assurance officers during on-site inspections
Skills
- Proven experience as a quality assurance manager or relevant role
- Thorough knowledge of methodologies of quality assurance and standards
- Excellent numerical skills and understanding of data analysis/statistical methods
- Good knowledge of MS Office and databases
- Outstanding communication skills
- Great attention to detail and a results driven approach
- Excellent organizational and leadership abilities
- Reliable and Trustworthy
- BSc/BA in science or a relevant field
- Familiarity with OLCC practices and Orelap guidelines
- Must be 21 years of age or older per OLCC rules
Job Type: Full-time
Pay: $20.00 - $24.00 per hour
Benefits:
- 401(k)
- 401(k) matching
- Dental insurance
- Employee assistance program
- Health insurance
- Life insurance
- Paid time off
- Retirement plan
- Vision insurance
Schedule:
- 8 hour shift
- Day shift
- Monday to Friday
Supplemental Pay:
- Bonus pay
Experience:
- Quality Assurance Managers: 1 year (Preferred)
Work Location: One location
Apply for this job with Pree Laboratories, 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.
Position Summary:
We are seeking an experienced Quality Assurance (QA) Manager to oversee our quality assurance program. The QA Manager will oversee the activity of the quality assurance and analytical laboratory departments and staff, developing, implementing, and maintaining a system of quality and reliability for the organization’s products and/or development process. You will collaborate with other department heads to implement changes to increase efficiency while still maintaining high levels of quality. Your primary goal will be to ensure all our products meet OMMU regulations and safety guidelines.
Essential Functions:
- Analyze current quality assessment techniques for inconsistencies and redundancy
- Collaborates with management to achieve most efficient and accurate quality assessments
- Creates and implements a GMP (Good Manufacturing Practices) module
- Creates and Implements an SSOP (Sanitation Standard Operating Procedures)
- Creates and modifies Standard Operating Procedures according to state regulations and production needs
- Follow products through the entirety of process to ensure each step is completed correctly
- Perform detailed inspections of cannabis products and confirm they are up to standards
- Track, record, and maintain quality assurance data
- Analyze results and schedule compliance audits and exterior sampling procedures
Qualifications:
- Bachelor’s degree required
- 3-5 years of experience as a department manager in a or manufacturing-based environment required
- Proficient in Windows 10 operating system, Microsoft Office
- Experience in Lean/Six Sigma work environment a plus
- Willing and able to work a flexible schedule with some weekend work and occasional travel
- Strong people management skills required
- Ability to communicate ideas and resolutions in a clear, concise, friendly manner
- Strong written and verbal communication skills
- Demonstrated ability to effectively multi-task and manage time both independently as well as within a team environment
- Continuous Process Improvement mindset
- Must be at least 21 years of age
- Must have a reliable personal vehicle
- Must be able to pass a background check in accordance with state regulations
Physical Requirements:
- Ability to sit, stand, and walk as needed
- Ability to bend at the waist, kneel, crouch to access equipment
- Ability to lift and carry up to 50lbs
- Close visual acuity needed for viewing screens and fine print
Workplace Environment
- Consistent moderate background noise level due to HVAC and machinery
- Exposure to cannabis odor
- Exposure to skin contact with plants, to which some individuals may be allergic
Apply for this job with INSA
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.
Position Summary:
We are seeking an experienced Quality Assurance (QA) Manager to oversee our quality assurance program. The QA Manager will oversee the activity of the quality assurance and analytical laboratory departments and staff, developing, implementing, and maintaining a system of quality and reliability for the organization’s products and/or development process. You will collaborate with other department heads to implement changes to increase efficiency while still maintaining high levels of quality. Your primary goal will be to ensure all our products meet OMMU regulations and safety guidelines.
Essential Functions:
- Analyze current quality assessment techniques for inconsistencies and redundancy
- Collaborates with management to achieve most efficient and accurate quality assessments
- Creates and implements a GMP (Good Manufacturing Practices) module
- Creates and Implements an SSOP (Sanitation Standard Operating Procedures)
- Creates and modifies Standard Operating Procedures according to state regulations and production needs
- Follow products through the entirety of process to ensure each step is completed correctly
- Perform detailed inspections of cannabis products and confirm they are up to standards
- Track, record, and maintain quality assurance data
- Analyze results and schedule compliance audits and exterior sampling procedures
Qualifications:
- Bachelor’s degree required
- 3-5 years of experience as a department manager in a or manufacturing-based environment required
- Proficient in Windows 10 operating system, Microsoft Office
- Experience in Lean/Six Sigma work environment a plus
- Willing and able to work a flexible schedule with some weekend work and occasional travel
- Strong people management skills required
- Ability to communicate ideas and resolutions in a clear, concise, friendly manner
- Strong written and verbal communication skills
- Demonstrated ability to effectively multi-task and manage time both independently as well as within a team environment
- Continuous Process Improvement mindset
- Must be at least 21 years of age
- Must have a reliable personal vehicle
- Must be able to pass a background check in accordance with state regulations
Physical Requirements:
- Ability to sit, stand, and walk as needed
- Ability to bend at the waist, kneel, crouch to access equipment
- Ability to lift and carry up to 50lbs
- Close visual acuity needed for viewing screens and fine print
Workplace Environment
- Consistent moderate background noise level due to HVAC and machinery
- Exposure to cannabis odor
- Exposure to skin contact with plants, to which some individuals may be allergic
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Responsibilities of the QA Flower Manager includes approving standard methods and procedures related to the production, processing, packaging, labeling and storage of cannabis as they relate to Quality and good manufacturing practices. The QA Flower manager is responsible for the distribution of all cannabis flower to each department. They act as a link between manufacturing and the farm. Working in tandem with farm QA manager to ensure the proper strains are flowing through to the corresponding brand form factors and packaging.
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Medical Cannabis Compliance Testing - Laboratory QA/QC Manager
Advanced Analytics Lab LLC.
About us
Advanced Analytics Lab LLC. is a small locally owned business in Fort Gibson, Oklahoma. We are collaborative, professional and data-driven.
Our work environment includes:
- Lively atmosphere
- Growth opportunities
- Relaxed atmosphere
- Casual work attire
- Flexible working hours
- Safe work environment
- Company perks
QA/QC Manager:
We are looking for a reliable Manager of Quality Assurance to ensure that all external and internal requirements are met before our product reaches our customers. You will be responsible for inspecting procedures and outputs and identifying mistakes or non-conformity issues. An excellent Quality Assurance Manager has eyes like a hawk and solid experience in quality control. The ideal candidate is a reliable and competent professional whose approval will be necessary for the continuation of a business life cycle. The goal is to assure the high quality of our operations and services aiming to the long-term success of our business.
Minimum Requirements:
- Education Required: BA or BS Degree in Related Science
- Experience Required: 2 years in a laboratory environment.
The QA/QC Manager is responsible for the following:
- The quality manager manages all aspects of quality in the lab as they pertain to the Quality Management System, Quality Manual, supporting documentation, SOPs, training of staff, and review of data.
- Be trained and proficient at each test method in the lab to enable evaluation of data objectively and perform assessments without influence.
- Have training and / or experience in QA/QC procedures and be knowledgeable in the ISO/IEC 17025.
- Ensures that the Quality Management System is established, implemented, and maintained in accordance with the ISO/IEC 17025:2017 and Oklahoma Medical Marijuana Authority.
- Have knowledge and expertise in the analytical test methods for which data review is to be performed.
- Manage the internal audit and data integrity program. Ensure full annual audits are completed.
- Notify laboratory management of deficiencies and performance of the quality system and be able to monitor corrective action.
- Review and revise SOP’s as needed in conjunction with laboratory analysts and laboratory management.
- Ensure training is being performed as needed and that the documentation is kept.
- Ensure that MDL's/LODS, IDOCs and DOCS are completed and calculated on a required frequency and that documentation is complete.
- Ensure daily method QC checks are being performed and that out-of-control situations are documented and corrected.
- Responsible for maintaining and updating the Quality Manual
- Make sure all testing personnel have the training and resources needed to complete the required testing
- Coordinate laboratory accreditation activities.
- Responsible for training all personnel on the Quality Management System and SOPs.
- Deputy to the following positions: In absence of one of the other positions the Quality Manger is responsible for the following positions: Laboratory Director, Senior Analyst, Analyst.
Job Types: Full-time, Contract
Pay: $50,000.00 - $65,000.00 per year
Benefits:
- Dental insurance
- Employee discount
- Flexible schedule
- Health insurance
- Paid time off
- Vision insurance
Schedule:
- 8 hour shift
- Day shift
- Monday to Friday
Supplemental Pay:
- Bonus pay
Ability to commute/relocate:
- Fort Gibson, OK 74434: Reliably commute or planning to relocate before starting work (Preferred)
Education:
- Bachelor's (Required)
Experience:
- ISO 17025: 1 year (Required)
- Analytical Cannabis Compliance Testing: 1 year (Required)
- Cannabis Laboratory QA/QC Management: 1 year (Required)
Shift availability:
- Day Shift (Preferred)
Work Location: One location
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Job Description:
The Quality Manager will maintain the QA/QC requirements for an ISO-17025 credited independent testing laboratory for cannabis. Responsibilities to include policy/procedure/work, instruction document generations, internal audits, managing proficiency testing, risk assessments, nonconforming work, and other tasks. This position will also assist in overseeing analytical laboratory testing services to further method validation and innovation. Experience with cannabis/hemp/CBD is strongly preferred.
Responsibilities:
· Ensure that Ace Laboratory achieves, maintains an excellent quality assurance program and is compliant with regulatory standards and proficiencies required by ISO 17025 and NevadaCCB.
· Generate and update SOPs, quality manual documents, and forms to meet regulatory compliance requirements and practical needs.
· Update, revise and maintain laboratory QA manual, SOP’s and other quality documents.
· Maintain training records for all lab staff and document management system.
· Lead auditor for internal audit and participate in Nevada CCB and ISO accreditation audits.
· Work with Laboratory Management to ensure corrective/preventative actions and complaints are addressed promptly and are effectively implemented.
· Adhere to all ISO and relevant regulations as they pertain to the position’s function and duties.
· Address quality concerns and complaints with clients, initiating CAPA as necessary.
· Perform, present, and implement CAPA as necessary for risk assessments
· Schedule, manage, review, and pass Proficiency Testing
· Assist lab manager in reviewing analytical reports, monitor turnaround times
· Approve method protocols, validations and data review as needed.
· Review Equipment qualification, calibration, and maintenance schedules and ensure they are adhered to.
· Assist in laboratory safety policy and procedures.
Skills & Qualifications:
· Bachelor of Science Degree in Chemistry, Biology, Environmental Science and 3-5 years laboratory experience
· Must be well versed in ISO 17025:2017
· Working knowledge of analytical chemistry and microbiology for manufacturing quality control.
· Preferred experience in hemp/cannabis analytical testing
· Knowledge of scientific method, data interpretation, and analyses.
· Experience with scientific research and technical writing.
· Proficiency with Microsoft Office Excel.
Desirable Skills:
· Thrives in a small company culture
· Helps to create a positive working environment through leading by example
· Self-starter that doesn’t require substantial oversight for understanding required tasks and prioritization.
Other:
- Must pass the required background check
- Must be at least 21 years old.
- Must be able to lift 20lbs
- Ace Analytical offers a competitive and comprehensive benefits package including health, dental, vision, and time off.
- Ace Analytical is an Equal Opportunity Employer- All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.
- Due to federal scheduling of cannabis, every potential employee must be authorized to work in the U.S. and no potential employee may be under an H-1B, L-1A, or L-1B visa, or any other employee-petitioned non-immigrant U.S. work authorization.
If you are interested, please submit your resume and a cover letter. Applications without cover letters will not be considered.
Job Type: Full-time
Benefits:
- Dental insurance
- Health insurance
- Paid time off
- Vision insurance
Schedule:
- Day shift
- Monday to Friday
- Night shift
Supplemental Pay:
- Bonus pay
Education:
- Bachelor's (Required)
Experience:
- Quality assurance: 1 year (Required)
- ISO 17025: 1 year (Required)
Work Location: One location
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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 Quality Assurance (QA) Manager to join our facility in Lincoln, IL. As a QA Manager, you will be responsible for overseeing quality-related activities at the facility associated with sampling and inspection of in-process and finished products, 3rd party testing, customer complaints, product investigations, and Corrective and Preventive Action (CAPA) plans. Product families may include cannabis flower, cannabis oil, and manufacturing infused products. This position will be responsible for ensuring products are being produced in a manner that meets all specifications and brand consistency. You will also lead efforts to identify potential quality risks and work 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
- Responsible for management of site QA staff.
- Performs in-process sampling and inspection.
- Performs finished product sampling and inspection.
- Performs equipment and product line clearances before production runs.
- Reviews 3rd party testing laboratory results, as necessary.
- Manages and writes customer complaints and product investigations, helping to assess risk, identify root cause, CAPA plans, and implementing solutions with business partners.
- Assist with QMS document writing and revisions, including routing and/or approval of change request packages.
- Inspects packaged orders to ensure correct content and quantities, as deemed necessary.
- Inspects retain samples, as deemed necessary.
- Reviews in-process batch documentation, logbooks, test results, and good documentation practices.
- Discusses issues and concerns directly with line personnel and operations management so any corrections and improvements can be made in a timely manner.
- Performs reviews and audits as assigned.
- Collaborates with operational functions to troubleshoot manufacturing and production defects, CAPA, and customer complaints. Provides advice with process improvements to eliminate errors and reduce risk.
- Consolidates technical information from operations and manufacturing personnel and prepares written investigation and CAPA reports which may be provided to state regulators. Discuss quality-related issues with state regulators, as needed.
- Monitors compliance to established Good Manufacturing Practice (GMP) and GFSI (Global Food Safety Initiative) guidance such as BRC, SQF, and FSSC 22000, if applicable.
- Facilitates creation of and/or updates to product safety plans or product process parameters.
- Provides recommendations for product discontinuation, quarantine, destruction, rework, withdrawal/recall to operations and quality management.
- Conducts all duties in compliance with safety rules, applicable SOPs, and other applicable guidelines.
- 5-10% travel to other facilities and states to help with new market launches, training, etc.
REQUIRED EXPERIENCE, EDUCATION, AND SKILLS
- Bachelors Degree, 5+ years experience in a quality role
- Prior experience in highly regulated industry: cannabis. healthcare, medical devices, pharmaceutical, consumer packaged goods (food). Highly desirable: Cannabis, FDA, HACCP, GFSI (Global Food Safety Initiative) such as BRC, SQF, and FSSC 22000.
- Prior experience in Quality Assurance or Quality Control function.
- Prior experience with product sampling, inspection procedures, customer complaints, product investigations, and CAPA.
- Prior experience in regulatory agency audits and correspondence.
- 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, including writing executive summaries and communicating with senior level operations, quality management team, and regulatory agencies.
- Detail-oriented
- Utilizes critical thinking to troubleshoot issues, work collaboratively with a team to brainstorm solutions, and implement improvement solutions.
- Manage personnel, including performance management, setting vision, priorities, etc., if applicable.
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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TruTrace is a fully integrated software platform, secured on a blockchain infrastructure that gives clients the ability to store, manage, share and immediately access quality assurance and testing details, COAs, as well as motion and movement intelligence on inventory from batches and lots to serialized items.
The platform was specifically designed to power the traceability of testing standards within the medical cannabis, nutraceutical, food and pharmaceutical spaces with a focus on the authentication of source materials or ingredients used in formulation. An iteration of the core technology, called StrainSecure, is being utilized by Canada’s largest pharmacy chain, Shoppers Drug Mart, and is being leveraged by North America's largest health research institute, the University Health Network, in the first clinical trial of its kind. (https://ca.finance.yahoo.com/news/shoppers-drug-mart-aims-to-grow-medical-pot-sales-with-more-data-113255344.html)
We understand that delivering excellence starts with great talent, and that is where you come in.
Internship Role / Summary
In the role of Social Media & Quality Assurance Unicorn you will make meaningful contributions to our initiatives, have an impact on end results and walk away with an invaluable experience. You will work closely with a small team of topnotch talent to support Social Media marketing efforts and Quality Assurance testing. This includes but may not be limited to curating content and managing various Social Media channels, as well as the QA of website UI/UX, features and functionality. No coffee errands, mundane tasks or micro-management come with this role. Interns have traditionally loved the experience of working with us and we love them too.
We are looking for an initial 3-month commitment and all of the duties could be performed remotely.
What you’d do:
- Research and keep abreast of emerging behaviors, trends, and technologies for various verticals.
- Curate content and otherwise manage Social Media channels and outlets.
- Assist with the testing of key application features and functionality.
Prerequisites:
- High school degree or equivalent
- Ideally enrolled in college or working towards a degree / certification
- Superior communication skills, particularly as it relates to writing proficiency.
- Solid knowledge of Microsoft platforms, particularly Excel
- Exceptional knowledge of social media platforms and best practices
- Ability to work cooperatively and collaborate with others in a team environment
- Ability to document requirements, changes, procedures, and results.
- Ability to rapid compile research and provide thoughtful insight
- Ability to be flexible, agile, and responsive
- Always lead with a positive, solution-oriented attitude and having a sense of humor is a big plus
Bonus Skills:
- Adobe Premier Pro, After Effects and / or Photoshop experience
Upon securing the internship and assessing contribution, the intern may be offered compensation in the form of a TBD monthly stipend or bonus.
Job Type: Internship
Benefits:
- Employee Discount
- Flexible Schedule
- Professional Development Assistance
Schedule:
- Monday to Friday
Education:
- High school or equivalent (Required)
Language:
- English (Required)
Work authorization:
- United States (Required)
Additional Compensation:
- Other forms
Work Location:
- Fully Remote
This Job Is:
- A good job for someone just entering the workforce or returning to the workforce with limited experience and education
- Open to applicants who do not have a college diploma
Company's website:
- https://trutrace.co/
Company's Facebook page:
- https://www.facebook.com/TruTrace
Work Remotely:
- Yes
Apply for this job with TruTrace Technologies, Inc
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About Anresco
Anresco Laboratories (est 1943) is a commercial analytical laboratory located in the Bayview of San Francisco. For the past 75 years we have provided testing services to food, pharmaceutical, and related industries. Over the past three plus years we have extended our service offerings to the cannabis industry, and now provide comprehensive testing services to cannabis cultivators, manufacturers, dispensaries, and distributors.
We are looking for a reliable Quality Assurance Manager to ensure that all external and internal requirements are met. The ideal candidate will be responsible for inspecting procedures and identifying mistakes or non-conformity issues. The goal is to assure the high quality of our operations and services aiming to the long-term success of our business.
Responsibilities
The position will focus on maintaining and improving the quality of analytical work performed at Anresco. The responsibilities include but not limited to:
- Devising procedures to inspect and report quality issues
- Monitoring all operations that affect quality
- Facilitating proactive solutions by collecting and analyzing quality data
- Reviewing current standards and policies
- Record keeping of quality reports, statistical reviews and relevant documentation
- Ensuring all legal standards are met
- Managing ISO 17025/FDA/ELAP/3rd party audits
- Writing and maintaining SOPs, logs, and data needed for ISO 17025 accreditation
- Generating training manuals for every level positions
- Assuring compliance with FDA and BCC quality standards
- Recommending improved workflow
- Listing with instrument manufacturers when servicing is needed
- Assisting with adding analyses to ISO 17025 scope of accreditation
- Tracking samples and liaising with the lab to ensure timely reporting of results
- Perform internal audits to maintain our Quality system
Skills
- Analytical capabilities and experience/knowledge of cannabis is preferred.
- Must have at least 2 years of experience as a QA/QC manager or 4 years working in QA/QC position.
- Able to provide technical and QA/QC training for analysts and new employees.
- Knowledge of general lab safety.
- Proven experience as a quality assurance manager or relevant role
- Thorough knowledge of methodologies of quality assurance and standards
- Excellent numerical skills and understanding of data analysis/statistical methods
- Good knowledge of MS Office and databases
- Outstanding communication skills
- Great attention to detail and a results driven approach
- Excellent organizational and leadership abilities
- Reliable and Trustworthy
Education and Experience
- The Quality Assurance Manager should have a minimum of a Bachelor’s degree in a science field or preferably a master's degree in Chemistry or Science with an emphasis on Chemistry.
- Must have at least 2 years of experience as a QA/QC manager or 4 years working in QA/QC position.
- Must be at least 21 years old
- Must be authorized to work in the United States
Benefits:
- 100% employer paid Kaiser medical insurance (alternative options available)
- Up to $850 HRA plan for medical deductible & copay expenses, dental expenses, and vision expenses
- Commuter pre-tax plan
- Corporate wellness plan
- 401k plan
Company Perks:
- 1st year retention bonus
- Semi-annual company performance bonus
- Accrued vacation
- Monthly company lunch
- Monthly company event (e.g. baseball games, happy hours)
- Daily free coffee, snacks, breakfast
- Regular performance and compensation reviews
Job Type: Full-time
Benefits:
- 401(k)
- Paid Time Off
Schedule:
- Monday to Friday
Experience:
- quality assurance: 1 year (Preferred)
Education:
- Bachelor's (Preferred)
Location:
- San Francisco, CA 94124 (Preferred)
Work authorization:
- United States (Required)
Additional Compensation:
- Bonuses
Work Location:
- One location
Company's website:
- https://anresco.com/
Benefit Conditions:
- Waiting period may apply
- Only full-time employees eligible
Work Remotely:
- No
Apply for this job with Anresco, Inc.
Apply now →
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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.
About Anresco
Anresco Laboratories (est 1943) is a commercial analytical laboratory located in the Bayview of San Francisco. For the past 75 years we have provided testing services to food, pharmaceutical, and related industries. Over the past three plus years we have extended our service offerings to the cannabis industry, and now provide comprehensive testing services to cannabis cultivators, manufacturers, dispensaries, and distributors.
We are looking for a reliable Manager of Quality Assurance to ensure that all external and internal requirements are met. The ideal candidate will be responsible for inspecting procedures and identifying mistakes or non-conformity issues. The goal is to assure the high quality of our operations and services aiming to the long-term success of our business.
Responsibilities
The position will focus on maintaining and improving the quality of analytical work performed at Anresco. The responsibilities include but not limited to:
- Devising procedures to inspect and report quality issues
- Monitoring all operations that affect quality
- Facilitating proactive solutions by collecting and analyzing quality data
- Reviewing current standards and policies
- Record keeping of quality reports, statistical reviews and relevant documentation
- Ensuring all legal standards are met
- Managing ISO/FDA/ELAP/3rd party audits
- Writing and maintaining SOPs, logs, and data needed for ISO accreditation
- Generating training manuals for every level positions
- Assuring compliance with FDA and BCC quality standards
- Recommending improved workflow
- Listing with instrument manufacturers when servicing is needed
- Assisting with adding analyses to ISO scope of accreditation
- Tracking samples and liaising with the lab to ensure timely reporting of results
Skills
- Proven experience as a quality assurance manager or relevant role
- Thorough knowledge of methodologies of quality assurance and standards
- Excellent numerical skills and understanding of data analysis/statistical methods
- Good knowledge of MS Office and databases
- Outstanding communication skills
- Great attention to detail and a results driven approach
- Excellent organizational and leadership abilities
- Reliable and Trustworthy
Education and Experience
- The Quality Assurance Manager should have a minimum of a Bachelor’s degree in a science field or an equivalent field or 4 years of relevant experience
- 3-5 years of Quality Assurance experience
- Must be at least 21 years old
- Must be authorized to work in the United States
Job Type: Full-time
Experience:
- quality assurance: 1 year (Preferred)
Education:
- Bachelor's (Preferred)
Work authorization:
- United States (Required)
Additional Compensation:
- Bonuses
Work Location:
- One location
Benefits:
- Health insurance
- Paid time off
Schedule:
- Monday to Friday
Company's website:
- https://anresco.com/
Benefit Conditions:
- Waiting period may apply
- Only full-time employees eligible
Apply for this job with Anresco, Inc.
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) Manager to join our FloraCal cultivation and processing facility in Santa Rosa, CA. This individual must be diverse in quality functions related to manufacturing, cultivation and supply chain. You will be responsible for overseeing quality-related activities at the facility associated with sampling and inspection, hold and release, product investigations, and Corrective and Prevention Action (CAPA) plans as well as support supply chain functions.The QA Manager will be responsible for Good Manufacturing Practices (GMP's) at the facility along with assisting with co-packers and Suppliers. Position will report directly into the Regional site Quality Director and indirectly to the Supplier QA Director. Product family would be cannabis flower. This position will be responsible for ensuring products are being produced in a manner that meets all specifications. You will also lead efforts to identify potential quality risks and working with operations personnel to develop improvement opportunities. The ideal candidate must possess strong leadership skills, strong attention to detail and have experience working within a highly regulated industry. The ideal candidate must be a change agent with strong influencing skills.
CORE JOB DUTIES
- Responsible for management of all quality related activities at the site. Intricate part of the site Leadership Team.
- Performs cannabis product sampling and inspection and disposition including hold, rework, and destruction.
- Develop and maintain cleaning schedules.
- Leads product investigations, helping to assess risk, identify root cause, CAPA plans, and implementing solutions with business partners.
- Track and evaluate all testing failures.
- Assist with QMS document writing and revisions, including routing and/or approval of change request packages.
- Reviews batch documentation, test results, and good documentation practices.
- Discusses issues and concerns directly with cultivation agent and cultivation operations management so any corrections and improvements can be made in a timely manner.
- Collaborates with operational functions to troubleshoot product defects, provides advice with process improvements to eliminate errors and reduce risk.
- Consolidates technical information from cultivation operations and prepares written investigation and CAPA reports which may be provided to state regulators.
- Monitors compliance to established Good Manufacturing Practice (GMP)
- Conducts all duties in compliance with safety rules, applicable SOPs, and other applicable guidelines.
- Travel to other internal facilities, co-packers, and suppliers across the U.S. to help with new market launches, training, inspections, auditing, risk assessments and other duties as assigned.
- Ensure all suppliers and co-packers are up to date with documentation
- Perform batch record review and release batches/lots.
REQUIRED EXPERIENCE, EDUCATION AND SKILLS
- Bachelor's Degree, 5+ years' experience in a quality role
- Prior experience in highly regulated industry: healthcare, medical devices, pharmaceutical, consumer packaged goods (food), cannabis. Highly desirable: FDA, HACCP, GFSI experience i.e. SQF, BRC, etc.
- Prior experience in Quality Assurance or Quality Control function
- Prior experience with supplier quality selection, supplier monitoring, supplier inspection procedures, and product withdrawal/recall procedures
- Prior experience with product sampling, inspection procedures, customer complaints, product investigations, and CAPA
- Prior experience in regulatory agency audits and correspondence.
- 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, including writing executive summaries and communicating with senior level operations, quality management team, and regulatory agencies
- Must be detail-oriented
- Utilizes critical thinking to troubleshoot issues, work collaboratively with a team to brainstorm solutions, and implement improvement solutions
- Manage personnel, including performance management, setting vision, priorities, etc.
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
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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.
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MISSION STATEMENT
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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 Manager to join our manufacturing facility in Marshall, MI. As the Quality Manager, you will be responsible for overseeing quality-related activities at the facility associated with incoming inspection, sampling and inspection of finished products, customer complaint investigations, product investigations, and Corrective and Preventive Action (CAPA) plans. Product families may include cannabis flower, cannabis oil, manufacturing infused products (lotion, capsules, vape pens/cartridges, transdermal patches), and food products (chocolate, gummies, cookies). This position will be responsible for ensuring products are being produced in a manner that meets all specifications and brand consistency. You will also lead efforts to identify potential quality risks and work 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
- Responsible for management of site QA staff.
- Performs finished product sampling and inspection.
- Performs equipment and product line clearances before production runs.
- Manages and writes customer complaints and product investigations, helping to assess risk, identify root cause, CAPA plans, and implementing solutions with business partners.
- Assist with QMS document writing and revisions, including routing and/or approval of change request packages.
- Inspects packaged orders to ensure correct content and quantities, as deemed necessary.
- Inspects retain samples and customer return samples, as deemed necessary.
- Reviews in-process batch documentation, logbooks, test results, and good documentation practices.
- Discusses issues and concerns directly with line personnel and operations management so any corrections and improvements can be made in a timely manner.
- Performs reviews and audits as assigned.
- Collaborates with operational functions to troubleshoot manufacturing and production defects, CAPA, and customer complaints. Provides advice with process improvements to eliminate errors and reduce risk.
- Consolidates technical information from operations and manufacturing personnel and prepares written investigation and CAPA reports which may be provided to state regulators. Discuss quality-related issues with state regulators, as needed.
- Monitors compliance to established Good Manufacturing Practice (GMP) and SQF (Safe Quality Foods) guidance.
- Facilitates creation of and/or updates to product safety plans or product process parameters.
- Provides recommendations for product discontinuation, quarantine, destruction, rework, withdrawal/recall to operations and quality management.
- Conducts all duties in compliance with safety rules, applicable SOPs, and other applicable guidelines.
- 5-10% travel to other facilities and states to help with new market launches, training, etc.
REQUIRED EXPERIENCE, EDUCATION AND SKILLS
- Bachelors Degree, 5+ years' experience in a quality role
- Prior experience in highly regulated industry: 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
- Prior experience in regulatory agency audits and correspondence.
- 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, including writing executive summaries and communicating with senior level operations, quality management team, and regulatory agencies
- Detail-oriented
- Utilizes critical thinking to troubleshoot issues, work collaboratively with a team to brainstorm solutions, and implement improvement solutions
- Manage personnel, including performance management, setting vision, priorities, etc.
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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) Manager to join our cultivation facility in Carpinteria, CA. As the QA Manager, you will be responsible for overseeing quality-related activities at the facility associated with sampling and inspection, hold and release, product investigations, and Corrective and Prevention Action (CAPA) plans. The QA Manager will be responsible for Good Manufacturing Practices (GMP's) at the facility. Product family would be cannabis flower. This position will be responsible for ensuring products are being produced in a manner that meets all specifications. You will also lead efforts to identify potential quality risks and working with cultivation operations personnel to develop improvement opportunities. The ideal candidate must possess strong leadership skills, strong attention to detail and have experience working within a highly regulated industry. The ideal candidate must be a change agent with strong influencing skills.
CORE JOB DUTIES
- Responsible for management of all quality related activities at the site. Intricate part of the site Leadership Team.
- Performs cannabis flower sampling and inspection and disposition including hold, rework, and destruction.
- Develop and maintain cleaning schedules.
- Leads product investigations, helping to assess risk, identify root cause, CAPA plans, and implementing solutions with business partners.
- Track and evaluate all testing failures.
- Assist with QMS document writing and revisions, including routing and/or approval of change request packages.
- Reviews batch documentation, test results, and good documentation practices.
- Discusses issues and concerns directly with cultivation agent and cultivation operations management so any corrections and improvements can be made in a timely manner.
- Participates in inspections and audits as needed or as assigned.
- Collaborates with operational functions to troubleshoot flower defects, provides advice with process improvements to eliminate errors and reduce risk.
- Consolidates technical information from cultivation operations and prepares written investigation and CAPA reports which may be provided to state regulators.
- Monitors compliance to established Good Manufacturing Practice (GMP)
- Conducts all duties in compliance with safety rules, applicable SOPs, and other applicable guidelines.
- 5-10% travel to other facilities and states to help with new market launches, training, etc.
REQUIRED EXPERIENCE, EDUCATION AND SKILLS
- Bachelor's Degree, 5+ years' experience in a quality role
- Prior experience in highly regulated industry: healthcare, medical devices, pharmaceutical, consumer packaged goods (food), cannabis. Highly desirable: FDA, HACCP, GFSI experience i.e. SQF, BRC, etc.
- Prior experience in Quality Assurance or Quality Control function
- Prior experience with product sampling, inspection procedures, customer complaints, product investigations, and CAPA
- Prior experience in regulatory agency audits and correspondence.
- 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, including writing executive summaries and communicating with senior level operations, quality management team, and regulatory agencies
- Detail-oriented
- Utilizes critical thinking to troubleshoot issues, work collaboratively with a team to brainstorm solutions, and implement improvement solutions
- Manage personnel, including performance management, setting vision, priorities, etc.
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.