Cannabis Quality Assurance Associate Jobs

We are an I-502 Recreational Cannabis Producer/Processor located in Factoria, WA. We are hiring (1) Full-time employee starting ASAP.

Daily Responsibilities of Quality Assurance Lead:

-Working (Monday - Friday) 9am-5pm. This position will be 50%-75% processing and 25%-50% Quality Assurance as needed. You will be working with our Processing managers as well as our Quality Assurance Lead.

*Quality Assurance Duties Include: Checking all orders for quality and matching to order manifest. Binning/boxing up for delivery drivers to pick up and deliver the following day. Helping to finalizing all delivery paperwork.

*Processing Duties Include: Processing orders for order fullfillment. Labeling mainly and some production of flower/joint units.

We have a fantastic team that loves what they do and where they do it. To be considered for this team we are looking for the following requirements:

-21+ with valid ID.
-Detail-oriented, punctual and good communication.
-Self-motivated with a positive attitude is a MUST!
-i502 Industry experience is not required but it's a plus.
-Must be able to work 40-45 hours a week.
-Must be able to stand/sit for long periods of time and lift up to 50lbs.
-Enjoy Team environment.

**Must provide your resume - including contact phone # & EMAIL**

Washington state law prohibits the consumption of alcohol or smoking of marijuana/cannabis at the place of business. We are a drug-free work place. Drug use on the clock or on the property will not be tolerated.

Work Remotely

• No

Job Type: Full-time

Pay: $17.00 - $18.00 per hour

Benefits:

• Employee discount
• Paid time off

Schedule:

• 8 hour shift

Supplemental pay types:

• Bonus pay

Education:

• High school or equivalent (Required)

Work Location: One location

Apply for this job with Hannah Industries

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 international provider of consumer products in cannabis, with a mission to improve lives by providing clarity around cannabis and confidence around consumption. As a high-growth cannabis company known for quality, expertise, and reliability, the company and its brands, including Curaleaf and Select provide industry-leading service, product selection, and accessibility across the medical and adult-use markets. In the United States, Curaleaf currently operates in 23 states with 130 dispensaries, 25 cultivation sites, and over 30 processing sites, and employs over 5,000 team members. Curaleaf International is the leading vertically integrated cannabis company in Europe with a unique supply and distribution network throughout the European market, bringing together pioneering science and research with cutting-edge cultivation, extraction, and production. Home | Curaleaf | Cannabis with Confidence

Our corporate social responsibility is Rooted In Good Diversity, Equity, Inclusion + Social Equity + Sustainability Social Responsibility | Curaleaf | Cannabis with Confidence We believe in taking corporate and social responsibility very seriously, from our educational outreach to national partnerships, state-wide initiatives and local causes. Giving back to the communities where we operate is important to us, and helps to change old attitudes by showing the positive impact of cannabis in creating jobs, changing lives, and helping local communities.

We educate. We advocate. We give.

Quality Assurance Senior Associate

The Quality Assurance Specialist will be responsible for supporting the Quality Assurance group to enforce processing and manufacturing procedures, technology, and business practices documented in State-level SOPs, policies, forms, and batch records. This role will support ongoing operations within the State, working closely with state and regional leaders to continuously improve operations. The QA Specialist will also be responsible for supporting training employees using the Quality Management System, periodic verification of batch records, and confirm product quality requirements are met. This role will closely communicate with other Curaleaf teams including, but not limited to: Compliance, Operations, and Cultivation.

Responsibilities:

• Monitor and ensure traceability of plant/product movement throughout the facility


• Perform or assist in quality inspections, auditing against cGMP criteria and confirming established product quality requirements are achieved.


• Assist with edits and review of state-specific and applicable national SOPs, policies, and supporting documents.


• Promptly communicate identified discrepancies to QA leadership and Operational team leads, and document accordingly.


• Investigate and participate in quality event investigations and reporting including CAPA, OOS reports, product quality complaints, and adverse event investigations.


• Assist with training team members on processes and procedures using approved documents.


• Perform accurate audit and inspections of cultivation/processing facilities using documentation provided to ensure compliance with internal and regulatory requirements and promptly report results to QA and Compliance leadership.


• Assist with document management including SOPs, work instructions, and visual aids in the eQMS and within the facility.


• Support QA leadership in implementing and maintaining a quality management system including the eQMS


• Perform periodic review of procedures, forms, logs and master batch records (MBRs).


• Maintain and enforce strict adherence to established procedures.


• Identify areas for quality control improvement and participate in problem solving activities to drive process improvements.


• Assist with change control for proposed changes to process or product


• Enforce safety and security procedures in compliance with OSHA and local EHS regulations; report potentially unsafe conditions; monitor for proper use of equipment and materials.


• Promote a culture of quality and change management.


• Additional duties and responsibilities will be assigned as necessary.

Qualifications:

• AS degree and 2+ years related experience, or 4+ years experience.


• Strong attention to detail.


• MS Office and Excel skills required.


• Excellent oral and written communication skills.


• Knowledge of cGMP or HACCP in food or manufacturing preferred.


• Results-driven and task-oriented.


• Flexible and creative, while maintaining a strong work ethic and the ability to meet critical deadlines.


• Ability to prioritize tasks.


• Excellent communication skills and ability to interact professionally at all levels of the organization, with vendors and stakeholders.

Details:

• This is a full-time onsite position for processing and cultivation locations.

Curaleaf is an Equal Opportunity Employer

Curaleaf is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.

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 international provider of consumer products in cannabis, with a mission to improve lives by providing clarity around cannabis and confidence around consumption. As a high-growth cannabis company known for quality, expertise, and reliability, the company and its brands, including Curaleaf and Select provide industry-leading service, product selection, and accessibility across the medical and adult-use markets. In the United States, Curaleaf currently operates in 23 states with 130 dispensaries, 25 cultivation sites, and over 30 processing sites, and employs over 5,000 team members. Curaleaf International is the leading vertically integrated cannabis company in Europe with a unique supply and distribution network throughout the European market, bringing together pioneering science and research with cutting-edge cultivation, extraction, and production. Home | Curaleaf | Cannabis with Confidence

Our corporate social responsibility is Rooted In Good Diversity, Equity, Inclusion + Social Equity + Sustainability Social Responsibility | Curaleaf | Cannabis with Confidence We believe in taking corporate and social responsibility very seriously, from our educational outreach to national partnerships, state-wide initiatives and local causes. Giving back to the communities where we operate is important to us, and helps to change old attitudes by showing the positive impact of cannabis in creating jobs, changing lives, and helping local communities.

We educate. We advocate. We give.

Quality Assurance Associate Job Summary:

The Quality Assurance Associate will be responsible for supporting the Quality Assurance group to enforce processing and manufacturing procedures, technology, and business practices documented in State-level SOPs, policies, forms, and batch records. This role will support ongoing operations within the State, working closely with state and regional leaders to continuously improve operations. The QA Associate will also be responsible for supporting training employees using the Quality Management System, periodic verification of batch records, and confirm product quality requirements are met. This role will closely communicate with other Curaleaf teams including, but not limited to: Compliance, Operations, and Cultivation.

Responsibilities:

• Assist in traceability exercises including mock recalls and plant inventory audits.


• Perform or assist in quality inspections, auditing against cGMP criteria and confirming established product quality requirements are achieved.


• Coordinate state-specific edits for applicable national SOPs, policies, and supporting documents.


• Promptly communicate identified discrepancies to QA leadership and Operational team leads, and document accordingly.


• Investigate and participate in quality event investigations and reporting including CAPA, OOS reports, product quality complaints, and adverse event investigations.


• Assist with training team members on processes and procedures using approved documents.


• Accurately complete documentation to ensure compliance with internal and regulatory requirements.


• Support site audits and inspections to ensure compliance with internal and regulatory requirements and promptly report results to QA.


• Assist with document management including SOPs, work instructions, and visual aids in the eQMS and within the facility.


• Support QA leadership in implementing and maintaining a quality management system including the eQMS


• Perform periodic review of procedures, forms, logs and master batch records (MBRs).


• Maintain


• and enforce strict adherence to established procedures.


• Identify areas for quality control improvement and participate in problem solving activities to drive process improvements.


• Assist with change control for proposed changes to process or product


• Enforce safety and security procedures in compliance with OSHA and local EHS regulations; report potentially unsafe conditions; use equipment and materials properly.


• Promote a culture of quality and change management.


• Additional duties and responsibilities will be assigned as necessary.

Qualifications:

• AS degree or technical certificate; or 2+ years related experience.


• Strong attention to detail.


• MS Office and Excel skills required.


• Excellent oral and written communication skills.


• Knowledge of cGMP or HACCP in food or manufacturing preferred.


• Results-driven and task-oriented.


• Flexible and creative, while maintaining a strong work ethic and the ability to meet critical deadlines.


• Ability to prioritize tasks.


• Excellent communication skills and ability to interact professionally at all levels of the organization, with vendors and stakeholders.

Curaleaf is an Equal Opportunity Employer

Curaleaf is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.

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 international provider of consumer products in cannabis, with a mission to improve lives by providing clarity around cannabis and confidence around consumption. As a high-growth cannabis company known for quality, expertise, and reliability, the company and its brands, including Curaleaf and Select provide industry-leading service, product selection, and accessibility across the medical and adult-use markets. In the United States, Curaleaf currently operates in 23 states with 130 dispensaries, 25 cultivation sites, and over 30 processing sites, and employs over 5,000 team members. Curaleaf International is the leading vertically integrated cannabis company in Europe with a unique supply and distribution network throughout the European market, bringing together pioneering science and research with cutting-edge cultivation, extraction, and production. Home | Curaleaf | Cannabis with Confidence

Our corporate social responsibility is Rooted In Good Diversity, Equity, Inclusion + Social Equity + Sustainability Social Responsibility | Curaleaf | Cannabis with Confidence We believe in taking corporate and social responsibility very seriously, from our educational outreach to national partnerships, state-wide initiatives and local causes. Giving back to the communities where we operate is important to us, and helps to change old attitudes by showing the positive impact of cannabis in creating jobs, changing lives, and helping local communities.

We educate. We advocate. We give.

Quality Assurance Associate

The Quality Assurance Associate will be responsible for supporting the Quality Assurance group to enforce processing and manufacturing procedures, technology, and business practices documented in State-level SOPs, policies, forms, and batch records. This role will support ongoing operations within the State, working closely with state and regional leaders to continuously improve operations. The QA Associate will also be responsible for supporting training employees using the Quality Management System, periodic verification of batch records, and confirm product quality requirements are met. This role will closely communicate with other Curaleaf teams including, but not limited to: Compliance, Operations, and Cultivation.

Responsibilities:

• Assist in traceability exercises including mock recalls and plant inventory audits.


• Perform or assist in quality inspections, auditing against cGMP criteria and confirming established product quality requirements are achieved.


• Coordinate state-specific edits for applicable national SOPs, policies, and supporting documents.


• Promptly communicate identified discrepancies to QA leadership and Operational team leads, and document accordingly.


• Investigate and participate in quality event investigations and reporting including CAPA, OOS reports, product quality complaints, and adverse event investigations.


• Assist with training team members on processes and procedures using approved documents.


• Accurately complete documentation to ensure compliance with internal and regulatory requirements.

• Support site audits and inspections to ensure compliance with internal and regulatory requirements and promptly report results to QA.

• Assist with document management including SOPs, work instructions, and visual aids in the eQMS and within the facility.


• Support QA leadership in implementing and maintaining a quality management system including the eQMS


• Perform periodic review of procedures, forms, logs and master batch records (MBRs).


• Maintain and enforce strict adherence to established procedures.


• Identify areas for quality control improvement and participate in problem solving activities to drive process improvements.


• Assist with change control for proposed changes to process or product


• Enforce safety and security procedures in compliance with OSHA and local EHS regulations; report potentially unsafe conditions; use equipment and materials properly.


• Promote a culture of quality and change management.


• Additional duties and responsibilities will be assigned as necessary.

Qualifications:

• AS degree or technical certificate; or 2+ years related experience.


• Strong attention to detail.


• MS Office and Excel skills required.


• Excellent oral and written communication skills.


• Knowledge of cGMP or HACCP in food or manufacturing preferred.


• Results-driven and task-oriented.


• Flexible and creative, while maintaining a strong work ethic and the ability to meet critical deadlines.


• Ability to prioritize tasks.


• Excellent communication skills and ability to interact professionally at all levels of the organization, with vendors and stakeholders.

Other Details:

• This is a full-time onsite position for processing and cultivation locations.

Curaleaf is an Equal Opportunity Employer

Curaleaf is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.

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.

ABOUT YOU
Are you passionate and ready to join an inclusive work environment, committed to leading new ideas and pathways, and to delivering value? If the answer is, “Yes!” then we have an exciting career opportunity for you. Who are we? We are Montrose, a leading environmental services company with 2,000+ employees across 70 locations worldwide, focused on supporting clients as they deal with the environmental challenges of today, and prepare for what’s coming tomorrow.
WHAT WE CAN OFFER YOU
Our Mission is: To help protect the air we breathe, the water we drink, and the soil that feeds us, and is supported by our Principles: We Value Our People, We Value Our Community, We Value Our Clients, We Value Our Shareholders. We care for the well-being of our people and offer:

• Competitive compensation packages
• Industry leading benefits packages including company paid life and disability insurance
• Paid parental leave benefits
• Progressive vacation policies and company holidays including floating holidays to meet the diverse needs of our people.
• 401(k) plan offered
• A financial assistance program to help support peers in need
• An educational reimbursement program
• Access to best rates in the industry to bring your student loan debt down to size

A DAY IN THE LIFE
Enthalpy Analytical, is part of the larger organization, Montrose Environmental Group, is comprised of over 9 laboratories servicing air, water, soil, tobacco, cannabis, and toxicity testing. Regulations drive the need for our services, but our unique capabilities allow us to add value to clients beyond environmental compliance.
Our Deer Park, TX Laboratory is currently seeking a Full-Time QA Associate to join our team. The QA Associate is an entry level role, assisting in ensuring that the laboratory’s data and Quality Assurance system meets regulatory and client requirements, with the goal of producing data of known and documented quality.
As a key member of the laboratory team, this role will be responsible for a full range of activities including:

• Perform peer and final review of environmental testing data
• Compile final reports, narrating deviations and outliers
• Collect, review, and interpret laboratory quality control data for performance and trends (logbooks, control charts, method detection and quantitation limit studies, performance testing samples)
• Organize and control laboratory documents, including procedures, forms, training records, and archived data
• Monitor the status of other quality assurance elements, such as support equipment calibrations
• Comply with Enthalpy’s Quality Assurance and Health and Safety Plans
• Other duties as assigned

NECESSARY QUALIFICATIONS
To perform this job successfully, individuals must be able to perform each duty and responsibility satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the duties and responsibilities.

• Undergraduate degree in Chemistry, Biology, Environmental Sciences or related sciences, or
• Previous laboratory experience that provides the knowledge, skills, and abilities to perform the job, through a combination of education, training, & experience.

PREFERRED SKILLS

• Strong working knowledge of MS Excel, Word, and other software used in generating documents and spreadsheets
• Strong attention to detail, with a focus on pattern recognition and consistency
• Good editorial and proofreading skills
• Good problem solving and troubleshooting abilities
• Effective written and oral communication skills
• Time management skills
• Ability to collaborate with lab team members to gain an understanding of laboratory processes, gather, interpret and consolidate data, generate documents and reports
• Working knowledge of analytical laboratory procedures

The above statements are intended to describe the general nature of work being performed by people assigned to this classification. They are not to be construed as an exhaustive list of all responsibilities, duties and skills required of employees so classified.
MAKE THE MOVE
From comprehensive air measurement and laboratory services to regulatory compliance, emergency response, permitting, engineering, and remediation, Montrose delivers innovative and practical design, engineering and operational solutions that keep its clients on top of their immediate needs – and well ahead of the strategic curve. We are a fast-paced and dynamic team. At Montrose, you
are your own boss, but you will get tons of guidance and plenty of support from talented, super-smart colleagues. Therefore, if freedom, autonomy, head-scratching professional challenges attract you, we’d love to speak with you.
Want to know more about us? Visit
montrose-env.com
and have fun!
Montrose is an Equal Opportunity Employer. Montrose is committed to providing access and reasonable accommodation in its employment for individuals with disabilities.

Apply for this job with Montrose Environmental Group, 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.

Curaleaf Holdings, Inc. (CSE: CURA) (OTCQX: CURLF) ("Curaleaf") is a leading international provider of consumer products in cannabis, with a mission to improve lives by providing clarity around cannabis and confidence around consumption. As a high-growth cannabis company known for quality, expertise, and reliability, the company and its brands, including Curaleaf and Select provide industry-leading service, product selection, and accessibility across the medical and adult-use markets. In the United States, Curaleaf currently operates in 23 states with 123 dispensaries, 25 cultivation sites, and over 30 processing sites, and employs over 5,000 team members. Curaleaf International is the leading vertically integrated cannabis company in Europe with a unique supply and distribution network throughout the European market, bringing together pioneering science and research with cutting-edge cultivation, extraction, and production. Home | Curaleaf | Cannabis with Confidence
Our corporate social responsibility is_ Rooted In Good_ Diversity, Equity, Inclusion + Social Equity + Sustainability Social Responsibility | Curaleaf | Cannabis with Confidence We believe in taking corporate and social responsibility very seriously, from our educational outreach to national partnerships, state-wide initiatives and local causes. Giving back to the communities where we operate is important to us, and helps to change old attitudes by showing the positive impact of cannabis in creating jobs, changing lives, and helping local communities.
We educate. We advocate. We give.
Quality Assurance Associate Job Summary:
The Quality Assurance Associate will be responsible for supporting the Quality Assurance group to enforce processing and manufacturing procedures, technology, and business practices documented in State-level SOPs, policies, forms, and batch records. This role will support ongoing operations within the State, working closely with state and regional leaders to continuously improve operations. The QA Associate will also be responsible for supporting training employees using the Quality Management System, periodic verification of batch records, and confirm product quality requirements are met. This role will closely communicate with other Curaleaf teams including, but not limited to: Compliance, Operations, and Cultivation.
Responsibilities:

• Assist in traceability exercises including mock recalls and plant inventory audits.
• Perform or assist in quality inspections, auditing against cGMP criteria and confirming established product quality requirements are achieved.
• Coordinate state-specific edits for applicable national SOPs, policies, and supporting documents.
• Promptly communicate identified discrepancies to QA leadership and Operational team leads, and document accordingly.
• Investigate and participate in quality event investigations and reporting including CAPA, OOS reports, product quality complaints, and adverse event investigations.
• Assist with training team members on processes and procedures using approved documents.
• Accurately complete documentation to ensure compliance with internal and regulatory requirements.
• Support site audits and inspections to ensure compliance with internal and regulatory requirements and promptly report results to QA.
• Assist with document management including SOPs, work instructions, and visual aids in the eQMS and within the facility.
• Support QA leadership in implementing and maintaining a quality management system including the eQMS
• Perform periodic review of procedures, forms, logs and master batch records (MBRs).
• Maintain
• and enforce strict adherence to established procedures.
• Identify areas for quality control improvement and participate in problem solving activities to drive process improvements.
• Assist with change control for proposed changes to process or productEnforce safety and security procedures in compliance with OSHA and local EHS regulations; report potentially unsafe conditions; use equipment and materials properly.
• Promote a culture of quality and change management.
• Additional duties and responsibilities will be assigned as necessary.

Qualifications:

• AS degree or technical certificate; or 2+ years related experience.
• Strong attention to detail.
• MS Office and Excel skills required.
• Excellent oral and written communication skills.
• Knowledge of cGMP or HACCP in food or manufacturing preferred.
• Results-driven and task-oriented.
• Flexible and creative, while maintaining a strong work ethic and the ability to meet critical deadlines.
• Ability to prioritize tasks.
• Excellent communication skills and ability to interact professionally at all levels of the organization, with vendors and stakeholders.

Other Details:

• This is a full-time onsite position for processing and cultivation locations.

Curaleaf is an Equal Opportunity Employer
Curaleaf is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.

Job Type: Full-time

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 international provider of consumer products in cannabis, with a mission to improve lives by providing clarity around cannabis and confidence around consumption. As a high-growth cannabis company known for quality, expertise, and reliability, the company and its brands, including Curaleaf and Select provide industry-leading service, product selection, and accessibility across the medical and adult-use markets. In the United States, Curaleaf currently operates in 23 states with 123 dispensaries, 25 cultivation sites, and over 30 processing sites, and employs over 5,000 team members. Curaleaf International is the leading vertically integrated cannabis company in Europe with a unique supply and distribution network throughout the European market, bringing together pioneering science and research with cutting-edge cultivation, extraction, and production. Home | Curaleaf | Cannabis with Confidence

Our corporate social responsibility is Rooted In Good Diversity, Equity, Inclusion + Social Equity + Sustainability Social Responsibility | Curaleaf | Cannabis with Confidence We believe in taking corporate and social responsibility very seriously, from our educational outreach to national partnerships, state-wide initiatives and local causes. Giving back to the communities where we operate is important to us, and helps to change old attitudes by showing the positive impact of cannabis in creating jobs, changing lives, and helping local communities.

We educate. We advocate. We give.

Quality Assurance Associate Job Summary:

The Quality Assurance Associate will be responsible for supporting the Quality Assurance group to enforce processing and manufacturing procedures, technology, and business practices documented in State-level SOPs, policies, forms, and batch records. This role will support ongoing operations within the State, working closely with state and regional leaders to continuously improve operations. The QA Associate will also be responsible for supporting training employees using the Quality Management System, periodic verification of batch records, and confirm product quality requirements are met. This role will closely communicate with other Curaleaf teams including, but not limited to: Compliance, Operations, and Cultivation.

Responsibilities:

• Assist in traceability exercises including mock recalls and plant inventory audits.


• Perform or assist in quality inspections, auditing against cGMP criteria and confirming established product quality requirements are achieved.


• Coordinate state-specific edits for applicable national SOPs, policies, and supporting documents.


• Promptly communicate identified discrepancies to QA leadership and Operational team leads, and document accordingly.


• Investigate and participate in quality event investigations and reporting including CAPA, OOS reports, product quality complaints, and adverse event investigations.


• Assist with training team members on processes and procedures using approved documents.


• Accurately complete documentation to ensure compliance with internal and regulatory requirements.


• Support site audits and inspections to ensure compliance with internal and regulatory requirements and promptly report results to QA.


• Assist with document management including SOPs, work instructions, and visual aids in the eQMS and within the facility.


• Support QA leadership in implementing and maintaining a quality management system including the eQMS


• Perform periodic review of procedures, forms, logs and master batch records (MBRs).


• Maintain


• and enforce strict adherence to established procedures.


• Identify areas for quality control improvement and participate in problem solving activities to drive process improvements.


• Assist with change control for proposed changes to process or productEnforce safety and security procedures in compliance with OSHA and local EHS regulations; report potentially unsafe conditions; use equipment and materials properly.


• Promote a culture of quality and change management.


• Additional duties and responsibilities will be assigned as necessary.

Qualifications:

• AS degree or technical certificate; or 2+ years related experience.


• Strong attention to detail.


• MS Office and Excel skills required.


• Excellent oral and written communication skills.


• Knowledge of cGMP or HACCP in food or manufacturing preferred.


• Results-driven and task-oriented.


• Flexible and creative, while maintaining a strong work ethic and the ability to meet critical deadlines.


• Ability to prioritize tasks.


• Excellent communication skills and ability to interact professionally at all levels of the organization, with vendors and stakeholders.

Other Details:

• This is a full-time onsite position for processing and cultivation locations.

Curaleaf is an Equal Opportunity Employer

Curaleaf is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.

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.

Truth Ent. is looking to hire a Full-time Quality Assurance Associate to add to our team!

Job Summary:

A Quality Assurance Associate performs a variety of tasks such as coordinating testing of bulk cannabis/manufactured goods, preparing labels for planned production runs, checking and inspecting loads received, checking accuracy and quality of materials reported from production on COC, data entry, maintaining records, cycle counts and other duties as needed.

Job Duties:

1. R&D/Compliance Testing

• Track all incoming/manufactured cannabis products and coordinate appropriate testing.

• Coordinate with cage associates to prepare testing batches for scheduled testing.

• Be present with the testing laboratory during testing to comply with compliance regulation.

• Track all testing results provided by labs and upload into appropriate ERP/Storage Systems.

• Communicates any failed COA or R&D testing with appropriate departments.

2. Label Production

• Compiles data from Passed COA's and/or ERP system to generate data needed to print on a label.

• Use systems to get secondary approval on labels before production.

• Coordinates label production based off of Planned Production Orders in accumatica ERP system prior to production.

Knowledge, skills, and qualifications:

• Minimum of 1-year experience with shipping, receiving and planning

• Knowledge of company products, weights and case /pallet counts

• Knowledge of shipping procedures, routes and rates

• Excellent communication and interpersonal skills

• Active listening skills

• Critical thinking skills

• Ability to maintain confidentiality

• Ability to multitask and prioritize duties

• Ability to follow through assignments with a minimum amount of direction

• Ability to coordinate many activities

• Ability to work positively in a team environment

• Great attention to detail and accuracy

• Must have excellent documentation skills

• Basic arithmetic, MS Word and Excel proficiency

• Familiar with UID / Metrc tags and processes

Physical Demands:

• Ability to frequently bend and/or twist at waist/knees/neck to and from seated position while working at workstation

• Ability to frequently communicate with others

• Ability to maintain long periods of mental alertness and attention to detail while setting priorities, meeting critical deadlines, and following up on assignments

• Ability to excessively stand and/or walk for extended periods of time

• Ability to seldom push and/or pull up to forty (40) pounds

• Ability to seldom lift or carry up to forty (40) pounds

• Ability to function in an environment with frequent interruptions

• Ability to deliver quality results under high pressure deadlines in a fast-paced environment

• Ability to demonstrate normal manual dexterity and eye-hand coordination

Work Hours:

Monday- Friday (9am-6pm)

Benefits:

• Medical, Dental, Vision

• 24 hours a year of paid sick leave

• Vacation depends on job tenure

Job Type: Full-time

Schedule:

• Monday to Friday

Experience:

• Quality Assurance: 3 years (Preferred)

Work Location:

• One location

Benefit Conditions:

• Waiting period may apply

Work Remotely:

• No

Apply for this job with Truth Enterprises

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.

This individual is responsible for supporting quality-related GMP activities occurring at manufacturing, and supply chain. This position will report to Quality Assurance Manager and work closely with Supply Chain representatives to support disposition activities for GMP materials (e.g. quality control workflows). This position will support the Quality Assurance Manager in ensuring products are being produced in a manner that meets all specifications. You will also support efforts to identify potential quality risks and working with manufacturing operations personnel to develop improvement opportunities. The Quality Assurance Associate will also provide quality support for related functions, including product manufacturing and quality system support. The successful candidate is self-motivated, independent, highly organized, able to work in a small team environment and adjust direction based on changing project/corporate priorities.

CORE JOB DUTIES

· Provide QA support for the review of analytical protocol, report and method review

· Support review for disposition of GMP materials, reviewing master and executed batch records, quality documents and other related paperwork

· Support release and disposition for Finished Product

· Review various documents such as batch records, technical reports, data, stability protocols and other GxP documents as needed

· Maintain logs for Quality systems, such as CAPA, Deviations, Investigations and Release Records

· Support the identification and investigation of quality related complaints or deviations, identifying and resolving root causes

· Support external/internal audits and inspections

REQUIRED EXPERIENCE, EDUCATION, SKILLS

· Bachelor’s Degree, minimum 1 years’ experience in Pharmaceutical Industry in a related quality assurance role, or the equivalent combination of education, training and experience.

· Experience with reviewing and dispositioning GxP materials

· Ability to identify technical problems and suggest resolution of the issues

• Ability to follow written procedures and monitor others for adherence to written procedures

• Ability to create or update written procedures with site operations personnel

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

Job Type: Full-time

Pay: $15.00 - $20.00 per hour

Benefits:

• Paid Time Off

Experience:

• Quality Assurance/Quality Control: 1 year (Preferred)
• pharaceutical industry: 1 year (Preferred)

Education:

• Bachelor's (Required)

Work authorization:

• United States (Required)

Work Location:

• One location

This Job Is Ideal for Someone Who Is:

• Dependable -- more reliable than spontaneous
• Detail-oriented -- would rather focus on the details of work than the bigger picture

This Company Describes Its Culture as:

• Detail-oriented -- quality and precision-focused
• Innovative -- innovative and risk-taking
• Team-oriented -- cooperative and collaborative

Schedule:

• Monday to Friday
• Day shift

Company's website:

• https://www.greenrockhempholdings.com/

Benefit Conditions:

• Only full-time employees eligible

Work Remotely:

• No

Apply for this job with Green Rock Hemp Holdings, 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.