1759 results
Quality Manager Cresco Labs Maryland, USA
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Quality Manager Cresco Labs Fall River, KS, USA
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Quality Manager Elixinol Broomfield, CO 80021
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Quality Manager Cresco Labs Wallkill, NY, USA
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Quality Manager

Cresco Labs Maryland, USA Full-time
Apply Now Copy link

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 manufacturing facility in Snow Hill, MD.

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, customer complaints, product investigations, and Corrective and Prevention Action (CAPA) plans.

Product families include cannabis oil, vape pens/cartridges, 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.

Performs in-process and finished product sampling and inspection Ensures equipment and product line clearances before production runs 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 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 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 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 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 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 and/or Associates Degree with equivalent experience 5+ years' experience in a quality role Prior experience in highly regulated industry:

healthcare, medical devices, pharmaceutical, consumer packaged goods (food), cannabis, 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 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 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

[{"employmentType":"Full-time","postedOn":"7 days ago","description":"<div><p>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.</p><p>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.</p><p>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.</p><p>Sunnyside</p><p>• , Cresco's national dispensary brand is a wellness-focused retailer designed to build trust, education and convenience for both existing and new cannabis consumers.</p><p>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.</p><p>MISSION STATEMENT At Cresco, we aim to lead the nation's cannabis industry with a focus on regulatory compliance, product consistency, and customer satisfaction.</p><p>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.</p><p>As Cresco grows, we will operate with the same level of professionalism and precision in each new market we move in to.</p><p>JOB SUMMARY Cresco Labs is seeking Quality Assurance (QA) Manager to join our manufacturing facility in Snow Hill, MD.</p><p>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, customer complaints, product investigations, and Corrective and Prevention Action (CAPA) plans.</p><p>Product families include cannabis oil, vape pens/cartridges, and concentrates.</p><p>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.</p><p>You will also lead efforts to identify potential quality risks and working with operations personnel to develop improvement opportunities.</p><p>The ideal candidate must possess a strong attention to detail and experience working within a highly regulated industry.</p><p>CORE JOB DUTIES.</p><p>Performs in-process and finished product sampling and inspection Ensures equipment and product line clearances before production runs 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 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 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.</p><p>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.</p><p>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 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 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.</p><p><b>REQUIRED EXPERIENCE, EDUCATION AND SKILLS Bachelors Degree and/or Associates Degree with equivalent experience 5+ years' experience in a quality role Prior experience in highly regulated industry:</b></p><p><b>healthcare, medical devices, pharmaceutical, consumer packaged goods (food), cannabis, or tobacco Highly desirable:</b></p><p>FDA, HACCP, GFSI (Global Food Safety Initiative) such as BRC, SQF, and FSSC 22000 Prior experience in Quality Assurance or Quality Control function.</p><p>Prior experience with product sampling, inspection procedures, customer complaints, product investigations, and CAPA Prior experience in regulatory agency audits and correspondence.</p><p>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 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.</p><p>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 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</p></div>","company":{"website":"crescolabs.com","companyType":"Public/Established","name":"Cresco Labs","logoUrl":"/logos/cresco-labs-af2becc596b572034007bd7a7d918bdd.png"},"location":{"country":"United States","address":"Maryland, USA","stateProvince":"MD"},"frontendLink":"/job-posting/cresco-labs/quality-manager/90c81f0b1f96f0d114e9b7130df6f7c3","title":"Quality Manager","hash":"90c81f0b1f96f0d114e9b7130df6f7c3","postingUrl":"https://www.jobilize.com/amp/job/quality-manager-md-united-states-cresco-labs-hiring-now-job-immediately"},{"employmentType":"Full-time","postedOn":"11 days ago","description":"<div><p><b>Job Description</b></p><p><b>COMPANY OVERVIEW</b></p><p>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.</p><p><b>MISSION STATEMENT</b></p><p>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.</p><p><b>JOB SUMMARY</b></p><p>Cresco Labs is seeking Quality Assurance (QA) Manager to join our manufacturing facility in Fall River, MA. 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, customer complaints, product investigations, and Corrective and Prevention Action (CAPA) plans. The position will report directly into the Regional Site QA Director-East. Product families include cannabis flower, cannabis oil, manufacturing infused products (lotion, capsules, vape pens/cartridges), 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 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.</p><p><b>CORE JOB DUTIES</b></p><p>Performs in-process and finished product sampling and inspection. Ensures equipment and product line clearances before production runs. 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 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. 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. 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 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. 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.</p><p>REQUIRED EXPERIENCE, EDUCATION AND SKILLS</p><p>Bachelors Degree and/or Associates Degree with equivalent experience 5+ years' experience in a quality role Prior experience in highly regulated industry: healthcare, medical devices, pharmaceutical, consumer packaged goods (food), cannabis, 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</p><p><b>ADDITIONAL REQUIREMENTS</b></p><p>Must be 21 years of age or older to apply Must comply with all legal or company regulations for working in the industry</p><p>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</p></div>","company":{"website":"crescolabs.com","companyType":"Public/Established","name":"Cresco Labs","logoUrl":"/logos/cresco-labs-af2becc596b572034007bd7a7d918bdd.png"},"location":{"country":"United States","address":"Fall River, KS, USA","city":"Fall River","stateProvince":"KS"},"frontendLink":"/job-posting/cresco-labs/quality-manager/91120f01730ce6cc3dcbc653c48e828e","title":"Quality Manager","hash":"91120f01730ce6cc3dcbc653c48e828e","postingUrl":"https://www.whatjobs.com/job-for-Quality-Manager-in-Fall-River-coop282828625"},{"employmentType":"","postedOn":"12 days ago","description":"<div><p><b>Quality Manager</b></p><p><b>About Elixinol</b></p><p>Elixinol is a Colorado based CBD company seeking the best and the brightest employees in the industry. With deep roots in the hemp industry, Elixinol has been manufacturing and providing the highest-quality CBD hemp extracts in the world since its inception in 2014. We are currently growing and seeking high quality and highly motivated individuals to join our Operations corporate team.</p><p><b>Job Summary</b></p><p>The Quality Manager, reporting directly to the Director of Operations, will be responsible for managing and overseeing all quality assurance and quality control functions, supervising the quality assurance technicians, and working alongside the Operations team, among other responsibilities. The Quality Manager will be responsible for developing, implementing, and maintaining safety by directing the testing and quality assurance of Elixinol’s products and processes.</p><p><b>Responsibilities</b></p><ul><li>Recruit and train quality technicians.</li><li>Work with other department managers in the Colorado facility for day-to-day facility operations and provide Quality related support to other departments.</li><li>Manage facility related Audit Program and maintain Audit Schedule and Completion Log.</li><li>Propose standard operation procedures where needed, train to and implement SOPs, as well as complete verification of effectiveness reviews at predetermined intervals.</li><li>Responsible for certification applications, renewal, compliance and reporting, scheduling/hosting audit of GMP and SQF, and fulfillment of any resulting corrective actions.</li><li>Manage scheduling, review, and updating of Quality records and manage Product Quality Plan and environmental monitoring program.</li><li>Manage and maintain critical state product and sales registrations.</li><li>Manage and direct internal HACCP and workers safety plans/committees.</li><li>Manage internal audit program and prepare appropriate reports and discuss with related personnel. As well as initiate, follow up, document, review, and file corrective action reports/deviation reports and implement corrective actions when procedures are not followed.</li><li>Assist Director of Operations to ensure compliance with customers' requirements as they pertain to the facility and oversee and review client, customer, and user feedback.</li><li>Assist Customer Service in management and evaluation of customer complaints with regards to product quality. Active input into CRM software required.</li><li>Oversee performance of QA to perform own reviews on documents including MMRs (Master Manufacturing Records), BPRs (Batch Production Records), and COAs (Certificates of Analysis).</li><li>Oversee the incoming inspection and release of all primary product components, labels and retail packaging for production use.</li><li>QA Manager has the authority on distribution of the product for OOS results that impact the quality and composition of ingredients or products.</li><li>Determine Quality check frequency and perform quality checks on the packaging lines to ensure that final products meet quality expectations and specifications.</li><li>Assist Validation Program by overseeing QA technologist and/or sampling personnel to make sure samples are pulled properly and pass to QC for testing.</li><li>Fill out appropriate portions of QAR forms to document material disposition decisions for any OOS results and file appropriate material disposal forms for rejected products.</li><li>Oversee Quality Assurance for production process control and make product disposition decisions and document any deviations in finished products.</li><li>Oversee QA to issue and maintain case specific corrective action reports for Corrective Action Program that violate suppliers/processing facilities/labs and distribute deviation reports to related departments/personnel. Assist Director of Operations with maintenance of Approved Supplier List, management of vendor surveys and scheduling of on-site audits, as necessary.</li></ul><p><b>Qualifications</b></p><ul><li>B.S. or B.A degree in business, engineering, or related field to the products being developed</li><li>Minimum 7 years' experience in a similar role</li><li>3+ years of management experience in a supervisory role with direct reports</li><li>HACCP certified, SQF certified, and PCQI certified preferred</li></ul><p><b>Work Conditions</b></p><p>Standard office: Sitting, typing, speaking, answering phones, communicating with others, standing, bending, walking, and occasional driving required. Must be able to lift up to 25 pounds at a time.</p><p><b>Work Hours: </b> Normal business hours, occasional overtime required.</p><p><b>Job Type: </b> Full-time</p><p><b>Salary: </b> $67,000-$85,000/year</p><p><b>Education</b></p><ul><li>Bachelor's (Required)</li></ul><p><b>Work authorization</b></p><ul><li>United States (Required)</li></ul><p><b>Benefits</b></p><p>Excellent benefits package, eligible upon hire, including 10 paid holidays, 3 weeks of PTO, sick time, health insurance, company-paid life insurance, 401(k) match after 6 months of employment, product discounts - excellent overall benefits package.</p><p><i>This document describes the general nature and level of work performed by personnel assigned to this job classification. This document is not, however, an exhaustive list of all responsibilities, duties, and skills required of personnel so assigned. Elixinol reserves the right to add, revise, or delete job duties at any time.</i></p><p><i>Elixinol is both an Equal Opportunity, and At Will employer. The company does not discriminate on the basis of race, age, sex, religion, marital status, or sexual orientation. Either Company or Employee can terminate the employment relationship at any time for any legally permissible reason. Reasonable accommodations will be made for qualified candidates/employees with disabilities.</i></p><p>Job Type: Full-time</p><p>Pay: $67,000.00 - $85,000.00 per year</p><p>Benefits:</p><ul><li>401(k)</li><li>401(k) matching</li><li>Dental insurance</li><li>Employee assistance program</li><li>Employee discount</li><li>Flexible spending account</li><li>Health insurance</li><li>Health savings account</li><li>Life insurance</li><li>Paid time off</li><li>Parental leave</li><li>Professional development assistance</li><li>Vision insurance</li></ul><p>Schedule:</p><ul><li>8 hour shift</li><li>Monday to Friday</li></ul><p>COVID-19 considerations:<br />We require all staff and guests to wear masks at all times unless seated in office alone, social distancing, temperature checks upon entering building, routine cleanings, sanitization stations. We ensure our facility is a safe working environment.</p><p>Education:</p><ul><li>Bachelor's (Preferred)</li></ul><p>Experience:</p><ul><li>management: 3 years (Preferred)</li><li>similar role: 7 years (Preferred)</li></ul><p>License/Certification:</p><ul><li>HACCP certified, SQF certified, and PCQI certified (Preferred)</li></ul><p>Work Location:</p><ul><li>One location</li></ul><p>Work Remotely:</p><ul><li>No</li></ul></div>","company":{"companyType":"Public/Established","name":"Elixinol","logoUrl":"/logos/elixinol-2c3cedd7761e2a33a7bed7f207151b6c.png"},"location":{"country":"United States","address":"Broomfield, CO 80021","city":"Broomfield","stateProvince":"CO"},"frontendLink":"/job-posting/elixinol/quality-manager/2751f862bfdcc0e408885bce9e99b157","title":"Quality Manager","hash":"2751f862bfdcc0e408885bce9e99b157","postingUrl":"https://www.indeed.com/job/quality-manager-c39a6112320493b5"},{"employmentType":"Full-time","postedOn":"12 days ago","description":"<div><p>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</p><p>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</p><p>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</p><p>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</p><p>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</p><p>MISSION STATEMENT At Cresco, we aim to lead the nation's cannabis industry with a focus on regulatory compliance, product consistency, and customer satisfaction</p><p>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</p><p>As Cresco grows, we will operate with the same level of professionalism and precision in each new market we move in to</p><p>JOB SUMMARY Cresco Labs is seeking Quality Assurance (QA) Manager to initially support our manufacturing facility in Wallkill, NY</p><p>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, customer complaints, product investigations, and Corrective and Prevention Action (CAPA) plans</p><p>Product families include cannabis oil, vape pens/cartridges, and concentrates</p><p>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</p><p>You will also lead efforts to identify potential quality risks and working with operations personnel to develop improvement opportunities</p><p>The ideal candidate must possess a strong attention to detail and experience working within a highly regulated industry</p><p>CORE JOB DUTIES. * Performs in-process and finished product sampling and inspection. * Ensures equipment and product line clearances before production runs. * 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 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. * 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</p><p>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</p><p>Discuss quality-related issues with state regulators, as needed. * Monitors compliance to established Good Manufacturing Practice (GMP), Good Agricultural Practice (GAP) 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. * 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</p><p>REQUIRED EXPERIENCE, EDUCATION AND SKILLS * Bachelors Degree and/or Associates Degree with equivalent experience * 5+ years' experience in a quality role * Prior experience in highly regulated industry: healthcare, medical devices, pharmaceutical, consumer packaged goods (food), cannabis, 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 * 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 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</p></div>","company":{"website":"crescolabs.com","companyType":"Public/Established","name":"Cresco Labs","logoUrl":"/logos/cresco-labs-af2becc596b572034007bd7a7d918bdd.png"},"location":{"country":"United States","address":"Wallkill, NY, USA","city":"Wallkill","stateProvince":"NY"},"frontendLink":"/job-posting/cresco-labs/quality-manager/0512c01e9e63bc9a831c43bfdc288b39","title":"Quality Manager","hash":"0512c01e9e63bc9a831c43bfdc288b39","postingUrl":"https://us.jobrapido.com/jobpreview/1839243584"},{"postedOn":"16 days ago","description":"<div><div><h2><b>COMPANY OVERVIEW</b></h2><p>Recently named one of <i>Entrepreneur</i> 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.</p><h2><b>MISSION STATEMENT</b></h2><p>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.</p><p><b>JOB SUMMARY</b></p><p>Cresco Labs is seeking a Quality Manager to join our Fall River Facility. 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.</p><p>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 follows brand consistency. You will also lead efforts to identify potential quality risks and work with operations personnel to develop improvement opportunities.</p><p><b>CORE JOB DUTIES</b></p><ul><li>Responsible for management of site Quality Assurance staff</li><li>Performs finished product sampling and inspection</li><li>Performs equipment and product line clearances before production runs</li><li>Manages and writes customer complaints and product investigations, helping to assess risk, identify root cause, CAPA plans, and implementing solutions with business partners</li><li>Assist with QMS document writing and revisions, including routing and/or approval of change request packages</li><li>Inspects packaged orders to ensure correct content and quantities, as deemed necessary</li><li>Inspects retain samples and customer return samples, as deemed necessary</li><li>Reviews in-process batch documentation, logbooks, test results, and good documentation practices</li><li>Discusses issues and concerns directly with line personnel and operations management so any corrections and improvements can be made in a timely manner</li><li>Performs reviews and audits as assigned</li><li>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</li><li>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</li><li>Monitors compliance to established Good Manufacturing Practice (GMP) and SQF (Safe Quality Foods) guidance</li><li>Facilitates creation of and/or updates to product safety plans or product process parameters</li><li>Provides recommendations for product discontinuation, quarantine, destruction, rework, withdrawal/recall to operations and quality management</li><li>Conducts all duties in compliance with safety rules, applicable SOPs, and other applicable guidelines</li><li>5-10% travel to other facilities and states to help with new market launches, training, etc.</li></ul><p><b>REQUIRED EXPERIENCE, EDUCATION AND SKILLS</b></p><ul><li>Bachelors Degree and 5+ years' experience in a quality role</li><li>Prior experience in a highly regulated industry required (i.e.: healthcare, medical devices, pharmaceutical, consumer packaged goods (food), cannabis)</li><li>Prior experience managing and mentoring large teams, required</li><li>FDA, HACCP, and/or SQF experience, preferred</li><li>Prior experience in Quality Assurance or Quality Control function</li><li>Prior experience with product sampling, inspection procedures, customer complaints, product investigations, and CAPA</li><li>Prior experience with regulatory agency audits and correspondence</li><li>Ability to follow written procedures and monitor others for adherence to written procedures</li><li>Ability to create or update written procedures with site operations personnel</li><li>Strong written and verbal communication skills, including writing executive summaries and communicating with senior level operations, quality management team, and regulatory agencies</li><li>Utilizes critical thinking to troubleshoot issues, work collaboratively with a team to brainstorm solutions, and implement improvement solutions</li></ul><p><b>ADDITIONAL REQUIREMENTS</b></p><ul><li>Must be 21 years of age or older to apply</li><li>Must comply with all legal or company regulations for working in the industry</li></ul><p><i>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.</i></p></div></div>","company":{"companyType":"Public/Established","name":"Cresco Labs","logoUrl":"/logos/cresco-labs-af2becc596b572034007bd7a7d918bdd.png"},"location":{"country":"United States","address":"Fall River, MA","city":"Fall River","stateProvince":"MA"},"frontendLink":"/job-posting/cresco-labs/quality-manager/dfe327a6164f04fdbdbbc07da8e442f7","title":"Quality Manager","hash":"dfe327a6164f04fdbdbbc07da8e442f7","postingUrl":"https://www.indeed.com/job/quality-manager-a1e9d0d5b7473cd7"},{"postedOn":"13 days ago","description":"<div><div><div><p><b>Title: Quality Manager Department: Quality</b></p><p><b>Reporting To: Quality Director Status: Regular Full-Time, Exempt</b></p><p><b>Direct Reports: Quality team Location: CSA LA Lab</b></p></div><p><b>Job Summary</b></p><p>The Quality Manager is responsible for the implementation of CannaSafe’s quality program and ensuring all laboratory activities are in compliance with BCC regulations and ISO/IEC 17025 standards. This role is accountable for knowing and following all Company policies and standards, leads by example, and lives our values. This is a Full time on site postion.</p><p><b>Essential Duties and Responsibilities</b></p><ul><li>Lead the team with dynamic leadership that promotes an environment of support, development, engagement, and high productivity. This includes, but is not limited to, hiring, coaching, performance management, ensuring productivity, disciplinary action, cross-training, rewards and recognition, and succession planning.</li></ul><ul><li>Ensure quality assurance/control compliance and standardization. This requires maintaining current knowledge of internal and external standards, with particular focus on BCC and ISO/IEC 17025.</li></ul><ul><li>Create, manage, and facilitate the quality scorecard.</li></ul><ul><li>Effectively communicate quality policies and procedures to all levels of laboratory staff.</li></ul><ul><li>Establish and maintain documentation and record controls and procedures.</li></ul><ul><li>Develop and implement quality procedures and standards to ensure production activities meet compliance standards.</li></ul><ul><li>Create and update laboratory policies and procedures associated with various assays, in partnership with the Lab Director and Quality department.</li></ul><ul><li>Monitor laboratory data performance and customer complaints with tracking and establish corrective measures as needed. Prepare detailed reports, including current, trending, forecasting.</li></ul><ul><li>Manage internal and external audits. Investigate findings, work with the affected department(s) to develop appropriate corrective and/or preventive actions, document the findings, and perform appropriate follow-up. Evaluate the efficacy of implemented corrective/preventive methods.</li></ul><ul><li>Generate audit reports and schedule review with appropriate internal stakeholders.</li></ul><ul><li>Manage the proficiency testing (PT) program for the laboratory. This includes PT vendor evaluation, purchasing PT samples, scheduling PT tests, and reviewing submissions.</li></ul><ul><li>Monitor relevant data for performance and trends using statistical methods.</li></ul><ul><li>Build strong internal, external, and cross-functional relationships.</li></ul><ul><li>Other duties and special projects as assigned.</li></ul><p><b>Knowledge, Skills, and Abilities</b></p><ul><li>Ability to maintain an incredibly high degree of attention to detail and accuracy.</li></ul><ul><li>Ability to maintain confidence, confidentially, and composure during difficult and/or complex situations.</li></ul><ul><li>Ability to work in a dynamic, fast-paced deadline environment while successfully managing multiple tasks.</li></ul><ul><li>Strong knowledge of Microsoft Office, including Excel, PowerPoint, and Word.</li></ul><ul><li>Strong understanding of standard laboratory protocol.</li></ul><ul><li>Excellent communication skills and ability to effectively work, influence, problem solve, and communicate with all levels of the organization.</li></ul><ul><li>Proven track record in people leadership (supporting, developing, engaging) with demonstrated teambuilding and collaboration skills.</li></ul><ul><li>Proven track record in adapting to change and accelerating the performance of laboratory groups.</li></ul><ul><li>Demonstrated ability to be well balanced between the strategic view of the work and the execution aspect of the role.</li></ul><p><b>Education and Experience</b></p><ul><li>Required: A bachelor’s degree in a scientific discipline from a four-year college or university plus at least seven (7) years of relevant regulated industry experience (BCC, ISO, FDA, EPA, USP, etc.).</li></ul><ul><li>Required: Knowledge of principles, terminology, practices, techniques, and instrumentation commonly used in a laboratory setting.</li></ul><ul><li>Preferred: Supervisory/management experience.</li></ul><ul><li>Optional: Exposure to the cannabis industry.</li></ul><p><b>Essential Functions</b></p><p>The physical demands described here are representative of those that an employee must meet to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.</p><p>While performing the duties of this job the employee is frequently required to stand, handle or feel, to speak, and to hear. The employee is occasionally required to walk, sit, reach with hands and arms, bend, kneel, crouch, or crawl. The employee must frequently lift and/or move up to thirty-five (35) pounds. Specific vision abilities required for this job include close (proximity) vision, depth perception, and the ability to adjust focus.</p><p><b>Work Environment</b></p><p>The work environment described here is representative of that which an employee may encounter while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.</p><p>The standard analytical laboratory environment is one in which potential health hazards do exist. Administrative, operations, technical, and professional staff are expected to safely operate in accordance with applicable and appropriate health and safety policies and procedures, as prescribed by the applicable CannaSafe manuals and policies and/or federal, state, or local standards.</p><p>Laboratory staff can be expected to work in areas where hazards associated are with, but not limited to, airborne pathogens. Biological materials, hazardous substances, and radioactive material exist and are handled. Appropriate training is provided regarding these hazards and staff are expected to adhere to all health and safety policies at all times, whether they are in writing or verbalized by a supervisor.</p><div>A job description is representative of typical duties and responsibilities for the position and it is not all-inclusive. Other duties and responsibilities may be assigned by the Company to best suit business needs.</div></div><div></div></div>","company":{"companyType":"Private/Established","name":"CannaSafe","logoUrl":"/logos/cannasafe-0759740914f0eb80b569ecc26e94ac2b.png"},"location":{"country":"United States","address":"Van Nuys, CA 91406","city":"Van Nuys","stateProvince":"CA"},"frontendLink":"/job-posting/cannasafe/quality-manager/b681400a90acbe439443165cbfc07940","title":"Quality Manager","hash":"b681400a90acbe439443165cbfc07940","postingUrl":"https://www.indeed.com/job/quality-manager-9f66d3f86851264f"},{"employmentType":"Full-time","postedOn":"9 days ago","description":"<div><p><b>COMPANY OVERVIEW</b></p><p>Recently named one of Entrepreneur magazines 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, Crescos 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 Mindys, a line of edibles created by James Beard Award-winning chef Mindy Segal. Sunnyside*, Crescos 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 industrys 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.</p><p><b>MISSION STATEMENT</b></p><p>At Cresco, we aim to lead the nations 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.</p><p><b>JOB SUMMARY</b></p><p>Cresco Labs is seeking Quality Assurance (QA) Manager to initially support our manufacturing facility in Wallkill, NY, but long-term location would be based out of Endicott, NY. 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, customer complaints, product investigations, and Corrective and Prevention Action (CAPA) plans. Product families include cannabis oil, vape pens/cartridges, 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.</p><p>CORE JOB DUTIES .</p><p>• Performs in-process and finished product sampling and inspection.</p><p>• Ensures equipment and product line clearances before production runs.</p><p>• Manages and writes customer complaint and product investigations, helping to assess risk, identify root cause, plan CAPA activities, and implement solutions with business partners.</p><p>• Assist with QMS document writing and revisions, including routing and/or approval of change request packages.</p><p>• Inspects packaged orders to ensure correct content and quantities, as deemed necessary.</p><p>• Inspects retain samples and customer return samples, as deemed necessary.</p><p>• Manage and track stability sampling and testing per state regulation.</p><p>• Reviews batch manufacturing records, logbooks, test results, and ensures good documentation practices are followed.</p><p>• Discusses issues and concerns directly with line personnel and operations management so any corrections and improvements can be made in a timely manner.</p><p>• Performs GMP facility inspections.</p><p>• Participates in corporate Quality internal audits as assigned.</p><p>• 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.</p><p>• 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.</p><p>• Monitors compliance to established Good Manufacturing Practice (GMP), Good Agricultural Practice (GAP) and GFSI (Global Food Safety Initiative) guidance such as BRC, SQF, and FSSC 22000</p><p>• Facilitates creation of and/or updates to product safety plans or product process parameters.</p><p>• Overall accountability for product discontinuation, quarantine, destruction, rework, withdrawal/recall to operations and quality management.</p><p>• Conducts all duties in compliance with safety rules, applicable SOPs, and other applicable guidelines.</p><p>• 5-10% travel to other facilities and states to help with new market launches, training, etc.</p><p>REQUIRED EXPERIENCE, EDUCATION AND SKILLS</p><p>• Bachelors Degree and/or Associates Degree with equivalent experience</p><p>• 5+ years experience in a quality role</p><p>• Prior experience in highly regulated industry: healthcare, medical devices, pharmaceutical, consumer packaged goods (food), cannabis, or tobacco.</p><p>• Highly desirable: FDA, HACCP, GFSI (Global Food Safety Initiative) such as BRC, SQF, and FSSC 22000</p><p>• Prior experience in Quality Assurance or Quality Control function.</p><p>• Prior experience with product sampling, inspection procedures, customer complaints, product investigations, and CAPA</p><p>• Prior experience in regulatory agency audits and correspondence.</p><p>• Ability to follow written procedures and monitor others for adherence to written procedures</p><p>• Ability to create or update written procedures with site operations personnel</p><p>• Strong written and verbal communication skills, including writing executive summaries and communicating with senior level operations, quality management team, and regulatory agencies</p><p>• Utilizes critical thinking to troubleshoot issues, work collaboratively with a team to brainstorm solutions, and implement improvement solutions</p><p>• Able to manage personnel effectively, including performance issues, setting vision, priorities, etc.</p><p>• Demonstrates high sense of urgency and proactive thinking</p><p>• Experience with Continuous Improvement initiatives is a plus</p><p>• Experience with Good Agricultural Practice (GAP) is a plus</p><p><b>ADDITIONAL REQUIREMENTS</b></p><p>• Must be 21 years of age or older to apply</p><p>• Must comply with all legal or company regulations for working in the industry</p><p>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</p></div>","company":{"website":"crescolabs.com","companyType":"Public/Established","name":"Cresco Labs","logoUrl":"/logos/cresco-labs-af2becc596b572034007bd7a7d918bdd.png"},"location":{"country":"United States","address":"Endicott, NY, USA","city":"Endicott","stateProvince":"NY"},"frontendLink":"/job-posting/cresco-labs/jooble-quality-manager/afd0f9da0e3fed55015986fe2ed30576","title":"Jooble - Quality Manager","hash":"afd0f9da0e3fed55015986fe2ed30576","postingUrl":"https://jooble.org/jdp/-7059782221939846121/Quality-Manager-Endicott%2C-NY"},{"employmentType":"Full-time","postedOn":"12 days ago","description":"<div><p>An accredited top cannabis testing lab in Los Angeles is looking for a Quality Manager to join their team!</p><p><b>Job Summary: </b></p><p>The Quality Manager is responsible for the implementation of the lab’s quality program and ensuring all laboratory activities are in compliance with BCC regulations and ISO/IEC 17025 standards.</p><p><b>Job Duties: </b></p><p>· Lead the team with dynamic leadership that promotes an environment of support, development, engagement, and high productivity. This includes, but is not limited to, hiring, coaching, performance management, ensuring productivity, disciplinary action, cross-training, rewards and recognition, and succession planning.</p><p>· Ensure quality assurance/control compliance and standardization. This requires maintaining current knowledge of internal and external standards, with particular focus on BCC and ISO/IEC 17025.</p><p>· Create, manage, and facilitate the quality scorecard.</p><p>· Effectively communicate quality policies and procedures to all levels of laboratory staff.</p><p>· Establish and maintain documentation and record controls and procedures.</p><p>· Develop and implement quality procedures and standards to ensure production activities meet compliance standards.</p><p>· Create and update laboratory policies and procedures associated with various assays, in partnership with the Lab Director and Quality department.</p><p>· Monitor laboratory data performance and customer complaints with tracking and establish corrective measures as needed. Prepare detailed reports, including current, trending, forecasting.</p><p>· Manage internal and external audits. Investigate findings, work with the affected department(s) to develop appropriate corrective and/or preventive actions, document the findings, and perform appropriate follow-up. Evaluate the efficacy of implemented corrective/preventive methods.</p><p>· Generate audit reports and schedule review with appropriate internal stakeholders.</p><p>· Manage the proficiency testing (PT) program for the laboratory. This includes PT vendor evaluation, purchasing PT samples, scheduling PT tests, and reviewing submissions.</p><p>· Monitor relevant data for performance and trends using statistical methods.</p><p>· Build strong internal, external, and cross-functional relationships.</p><p>· Other duties and special projects as assigned.</p><p><b>Requirements: </b></p><p>· Ability to maintain an incredibly high degree of attention to detail and accuracy.</p><p>· Ability to maintain confidence, confidentially, and composure during difficult and/or complex situations.</p><p>· Ability to work in a dynamic, fast-paced deadline environment while successfully managing multiple tasks.</p><p>· Strong knowledge of Microsoft Office, including Excel, PowerPoint, and Word.</p><p>· Strong understanding of standard laboratory protocol.</p><p>· Excellent communication skills and ability to effectively work, influence, problem solve, and communicate with all levels of the organization.</p><p>· Proven track record in people leadership (supporting, developing, engaging) with demonstrated teambuilding and collaboration skills.</p><p>· Proven track record in adapting to change and accelerating the performance of laboratory groups.</p><p>· Demonstrated ability to be well balanced between the strategic view of the work and the execution aspect of the role.</p><p>· Required: A bachelor’s degree in a scientific discipline from a four-year college or university plus at least seven (7) years of relevant regulated industry experience (BCC, ISO, FDA, EPA, USP, etc.).</p><p>· Required: Knowledge of principles, terminology, practices, techniques, and instrumentation commonly used in a laboratory setting.</p><p>· Preferred: Supervisory/management experience.</p><p>· Preferred: Exposure to the cannabis industry.</p><p><b>Benefits Include: </b></p><p>Health, dental, and vision insurance, 401k, paid time off, and floating holidays.</p><p><i>Cannabis Consulting Group provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.</i></p><p><i>This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.</i></p><p>Job Type: Full-time</p><p>Pay: Up to $90,000.00 per year</p><p>Benefits:</p><ul><li>Dental insurance</li><li>Health insurance</li><li>Paid time off</li><li>Vision insurance</li></ul><p>Schedule:</p><ul><li>8 hour shift</li><li>Monday to Friday</li></ul><p>Work Location:</p><ul><li>One location</li></ul><p>Work Remotely:</p><ul><li>No</li></ul></div>","company":{"companyType":"Private/Growth","name":"Cannabis Consulting Group","logoUrl":"/logos/canna-resource-group-00d8790a186447a65a99dc4b54db7f84.jpeg"},"location":{"country":"United States","address":"Los Angeles, CA 91406","city":"Los Angeles","stateProvince":"CA"},"frontendLink":"/job-posting/cannabis-consulting-group/cannabis-quality-manager/2c4cec38849f54cdd817ff9281820468","title":"Cannabis Quality Manager","hash":"2c4cec38849f54cdd817ff9281820468","postingUrl":"https://www.indeed.com/job/cannabis-quality-manager-21ae749e488d02a7"},{"employmentType":"Full-time","postedOn":"18 days ago","description":"<div><p>Trovaro is a cannabis-focused staffing &amp; recruiting firm working with a variety of clients across the U.S. and Canada. This role is with a powerhouse client based in Chicago, IL with offices located across the U.S.</p><p>Cannabis experience required</p><p><b>About the Role:</b></p><p>We're seeking a Product Quality Assurance Manager to join our team.</p><p>You will be responsible for overseeing innovation quality specific to Flowers &amp; Extracts across the enterprise. Associated quality activities involve serving as process owner, subject matter expert, and Gatekeeper for the category through out the stage-gate process. This position will be responsible for ensuring products are being designed and launched in a manner that meets all specifications and brand consistency. You will also lead efforts to track and trend product issues post launch and identify potential quality risks while working with operations and R&amp;D personnel to develop improvement opportunities. The ideal candidate must demonstrate strong leadership, be a strong communicator, have a breadth of quality experience, and ability to work within a highly regulated industry.</p><p><b>Core Duties:</b></p><p>• Assists in the development of brand and product quality standards for all product categories: flower and flower products; oils, extracts and medicinal; infused edibles and beverages</p><p>• Leading product quality expert throughout the product innovation process and product commercialization including monitoring, investigations and technical CAPA in relations to quality and safety complaints of new products</p><p>• Leads the quality aspect of new products’ line extensions to various sites</p><p>• Ensures facilities launching new products are fully equipped with all quality documentation and quality personnel are properly trained to guarantee a successful integration.</p><p>• Manages new product trial assessments from a quality perspective and an active approver of all new products prior to launch.</p><p>• Subject matter expert for site quality personnel in relations to new products and launches.</p><p>• Assesses all new equipment and manufacturing processes for products safety and quality risks to ensure equipment is suitable for the intended process and products</p><p>• Serves as an escalation point for product quality issues that span across multiple sites, products, etc.</p><p>• Provides technical support to the Quality Systems Director in the development of Food Safety and Product Quality Plans for new products – responsible for the ingredient and process risk assessments</p><p>• Leads the development and maintenance of Product Quality Specifications for all product categories – partners with R&amp;D managers to develop technical product parameters and ensure adherence to specified limits</p><p>• Conducts all duties in compliance with safety rules, applicable SOPs, and other applicable guidelines.</p><p>• 25-30% to facilities and states as the need arises</p><p><b>Required Skills &amp; Education:</b></p><p>• Bachelor’s degree (in Food Science, Biology, Chemistry preferred), 5+ years’ experience in a quality role.</p><p>• Prior experience in highly regulated industry: healthcare, medical devices, pharmaceutical, consumer packaged goods (food), cannabis. Highly desirable: FDA/FSMA, HACCP, GFSI experience i.e. SQF, BRC, etc.</p><p>• Prior experience with manufacturing quality, stability programs, product development, sampling and testing, packaging and labeling, batch record reviews, product inspections, batch/lot release, material quarantine, product withdrawals/recalls.</p><p>• Strong written and verbal communication skills, including writing executive summaries and communicating with senior level operations, quality management team, and regulatory agencies</p><p>• Detail-oriented</p><p>• Ability to work autonomously and timely in a fast pace growing environment</p><p>• Utilizes critical thinking to troubleshoot issues, work collaboratively with a team to brainstorm solutions, and implement improvement solutions</p><p><b>ADDITIONAL REQUIREMENTS:</b></p><p>• Must be 21 years of age or older to apply</p><p>• Must comply with all legal or company regulations for working in the industry</p></div>","company":{"companyType":"Private/Startup","name":"Trovaro","logoUrl":"/logos/trovaro-880b6e5aae3e26c4d6293c45d7ccb8f7.png"},"location":{"country":"United States","address":"Chicago, IL, USA (+1 other)","city":"Chicago","stateProvince":"IL"},"frontendLink":"/job-posting/trovaro/cannabis-product-quality-manager/e742634fa71da9b28b4e1e02d1a63278","title":"Cannabis Product Quality Manager","hash":"e742634fa71da9b28b4e1e02d1a63278","postingUrl":"https://www.recruit.net/job/product-quality-manager-jobs/9EFC4443E7C1EBDA"},{"employmentType":"Full-time","postedOn":"22 days ago","description":"<div><p>Trovaro is a cannabis-focused staffing &amp; recruiting firm working with a variety of clients across the U.S. and Canada. This role is with a powerhouse client based in Chicago, IL with offices located across the U.S.</p><p><b>About the Role:</b></p><p>We're seeking a Product Quality Assurance Manager (Flower &amp; Extracts) to join the Chicago headquarters. You will be responsible for overseeing innovation quality specific to Flowers &amp; Extracts across the enterprise. Associated quality activities involve serving as process owner, subject matter expert, and Gatekeeper for the category through out the stage-gate process. This position will be responsible for ensuring products are being designed and launched in a manner that meets all specifications and brand consistency. You will also lead efforts to track and trend product issues post launch and identify potential quality risks while working with operations and R&amp;D personnel to develop improvement opportunities. The ideal candidate must demonstrate strong leadership, be a strong communicator, have a breadth of quality experience, and ability to work within a highly regulated industry.</p><p><b>Core Duties:</b></p><p>• Assists in the development of brand and product quality standards for all product categories: flower and flower products; oils, extracts and medicinal; infused edibles and beverages</p><p>• Leading product quality expert throughout the product innovation process and product commercialization including monitoring, investigations and technical CAPA in relations to quality and safety complaints of new products</p><p>• Leads the quality aspect of new products’ line extensions to various sites</p><p>• Ensures facilities launching new products are fully equipped with all quality documentation and quality personnel are properly trained to guarantee a successful integration.</p><p>• Manages new product trial assessments from a quality perspective and an active approver of all new products prior to launch.</p><p>• Subject matter expert for site quality personnel in relations to new products and launches.</p><p>• Assesses all new equipment and manufacturing processes for products safety and quality risks to ensure equipment is suitable for the intended process and products</p><p>• Serves as an escalation point for product quality issues that span across multiple sites, products, etc.</p><p>• Provides technical support to the Quality Systems Director in the development of Food Safety and Product Quality Plans for new products – responsible for the ingredient and process risk assessments</p><p>• Leads the development and maintenance of Product Quality Specifications for all product categories – partners with R&amp;D managers to develop technical product parameters and ensure adherence to specified limits</p><p>• Conducts all duties in compliance with safety rules, applicable SOPs, and other applicable guidelines.</p><p>• 25-30% to facilities and states as the need arises</p><p><b>Required Skills &amp; Education:</b></p><p>• Bachelor’s degree (in Food Science, Biology, Chemistry preferred), 5+ years’ experience in a quality role.</p><p>• Prior experience in highly regulated industry: healthcare, medical devices, pharmaceutical, consumer packaged goods (food), cannabis. Highly desirable: FDA/FSMA, HACCP, GFSI experience i.e. SQF, BRC, etc.</p><p>• Prior experience with manufacturing quality, stability programs, product development, sampling and testing, packaging and labeling, batch record reviews, product inspections, batch/lot release, material quarantine, product withdrawals/recalls.</p><p>• Strong written and verbal communication skills, including writing executive summaries and communicating with senior level operations, quality management team, and regulatory agencies</p><p>• Detail-oriented</p><p>• Ability to work autonomously and timely in a fast pace growing environment</p><p>• Utilizes critical thinking to troubleshoot issues, work collaboratively with a team to brainstorm solutions, and implement improvement solutions</p><p><b>ADDITIONAL REQUIREMENTS:</b></p><p>• Must be 21 years of age or older to apply</p><p>• Must comply with all legal or company regulations for working in the industry</p></div>","company":{"companyType":"Private/Startup","name":"Trovaro","logoUrl":"/logos/trovaro-880b6e5aae3e26c4d6293c45d7ccb8f7.png"},"location":{"country":"United States","address":"Berwyn Heights, MD","city":"Berwyn Heights","stateProvince":"MD"},"frontendLink":"/job-posting/trovaro/cannabis-product-quality-manager/e7e1a0aa1ca3db9ddf30ed063d970798","title":"Cannabis Product Quality Manager","hash":"e7e1a0aa1ca3db9ddf30ed063d970798","postingUrl":"https://www.jobilize.com/amp/job/cannabis-product-quality-manager-berwyn-heights-trovaro-united-states"},{"employmentType":"Full-time","postedOn":"2 days ago","description":"<div><p><b>Overview:</b></p><p>Our client, an Ontario-based producer and manufacturer of legal Cannabis Products, is in need of a Quality Assurance leader to take over the role of QAP for their organization. This position is to be based at the company’s primary production facility near Pearson Airport. Depending on the specific candidate this role can be pursued as either a contract role, or a full-time permanent position with benefits.</p><p><b>Responsibilities:</b></p><p>• Provide daily quality oversight for all Cannabis Act and GMP activities ensuring processes and practices are compliant with Health Canada and other global regulatory authorities.</p><p>• Develop, maintain, and administer an efficient and effective risk-based Quality Management System in compliance with regulatory requirements and industry recognized best practices for biologic commercial and clinical products.</p><p>• Defines and articulates the strategy for the overall philosophy, scope and key elements of quality systems as a member of the Senior Leadership Team.</p><p>• Engage in proactive relationships with Health Canada and other global regulatory authorities to facilitate the advancement of the Company’s objectives.</p><p>• When required, seek creative solutions and exert firm convictions in advancing the Company’s positions.</p><p>• Establish key performance indicators in alignment with company and operational goals; maintain and report applicable department and Quality System metrics.</p><p>• Drive continuous improvement and Operational Excellence culture of the Quality System from all levels of the organization thru self-detecting and self-correcting processes and systems and instilling strong ownership and accountability.</p><p>• Ensure site inspection and audit readiness at all times and lead regulatory and notified body inspections to positive outcomes.</p><p>• Proactively identify, assess, and mitigate quality, operational, and organizational risks; escalate key risks and issues.</p><p>• Develop and manage quality department’s annual operating budgets; partner with Finance to analyze variances and implement adjustments.</p><p>• Ensure the organization is trained to the highest standards of quality excellence and technical competency utilizing best in class processes and practices.</p><p>• Establish, improve and direct quality programs, policies and procedures to ensure compliance, corporate policies, and specific regulatory body guidelines.</p><p>• Create an environment that utilizes active thinking to generate creative solutions to complex technical problems stemming from investigations and equipment or process failures.</p><p>• Creates and maintains a quality culture of transparency and efficient communication of quality related matters to achieve and maintain the desired high level across the Company’s development and manufacturing operations.</p><p><b>Qualifications:</b></p><p>• A post-secondary degree in a related scientific field of study</p><p>• A career path demonstrating consistent success and growth within the Canadian pharmaceutical, food, or cannabis industries</p><p>• Demonstrated ability to work in a fast-paced environment without sacrificing standards</p><p>• Demonstrated ability to train, mentor and supervise staff</p></div>","company":{"companyType":"Private/Startup","name":"CCS Green","logoUrl":"/logos/ccs-green-2e6fa21f09e93495d42e32927165ae4f.png"},"location":{"country":"Canada","address":"Toronto, ON","city":"Toronto","stateProvince":"ON"},"frontendLink":"/job-posting/ccs-green/quality-assurance-manager-qap/da7a353fc781158b922db898d0502a5a","title":"Quality Assurance Manager (QAP)","hash":"da7a353fc781158b922db898d0502a5a","postingUrl":"https://cannabisjobs.net/job/46598/quality-assurance-manager-qap/"},{"employmentType":"Full-time","postedOn":"2 days ago","description":"<div><p><b>About Us</b></p><p>Common Citizen is proud to be a Michigan-based cannabis company committed to changing the social stigma that prevents people from enjoying the greater quality of life that cannabis can provide. Our company is founded on two principles: ‘cannabis for humanity’ and ‘change for the better’. ‘Cannabis for humanity’ meaning we put people first in everything we do – from our safe, high quality cannabis plants to our world-class customer experience to our caring workplace environment. ‘Change for the better’ meaning that we have an insatiable desire to make ourselves, our product and our team experience better each and every day. In fact, we are working hard to become and be recognized as a Great Place to Work® Best Workplaces in the USA.</p><p><b>About This Role</b></p><p>Every position at Common Citizen from seed to sale, is contributing to our mission to serve our fellow citizens of Michigan with the highest quality, safest cannabis product through our highly individualized and education-oriented provisioning centers. As such our growers, harvesters and trimmers are all called Cultivation Citizens.</p><p>The Quality Assurance Administrator is a subject matter expert responsible for developing engineering solutions in support of production operations. They are a key part of the Operations Technical Staff and they work on priority projects and initiatives: from fertigation and grow room production to post harvest trim and product packaging. Involvement will start in the design phase of new programs until production stabilizes. This is a dynamic environment requiring dynamic skills, and as such the daily tasks may vary, resulting in a fast paced and lively work environment. Citizens rely technical staff for support, quality control, Lean Deployment, and plant care.</p><p><b>Responsibilities</b><br />Outlined below is what we see you doing at this point in time. We are a fast-growing company looking for people that are excited to grow along with us.</p><ul><li>Assure that all raw materials, process parameters, sanitation procedures, and finished products comply with Customer, Company, State and Federal standards.</li><li>Must have HACCP certification and meet the requirements for PCQI and SQF Practitioner responsibilities.</li><li>Manage and audit quality programs and maintain proper documentation.</li><li>Administer hold product dispositions. Follow-up and coordinate the release and/or removal of hold product through the proper channels.</li><li>Assure that HACCP/Food Safety plans are fully implemented and monitored for all processing lines. Responsible for validating changes to food safety fundamentals (prerequisite programs).</li><li>Assure the training of employees in the areas of noncompliance, metal detection, GMP’s, HACCP, color code, and sanitation procedures.</li><li>Work with vendors to correct noncompliance issues concerning ingredients and supplies.</li><li>Provide technical assistance to team members regarding the use of chemicals and sanitation protocol. Duties to include verification of cleaning methods for control of microbial, allergenic, and organic product cross contamination risks.</li><li>Support the necessary retrieval of suspect product involved in a product recall.</li><li>Direct the implementation, process and follow-up to corrective action items for audits, and inspections by customers, MDA, FDA, etc.</li><li>Collect quality data and develop reports for business units.</li><li>Investigate consumer and customer complaints and provide written communication regarding the findings.</li></ul><p><b>The Experience You Bring and the Skills we Need: </b></p><ul><li>4 year B.S. degree in Food Science, Microbiology or related field desired.</li><li>Minimum of 10 years’ experience in food manufacturing business, preferably in the Quality Assurance or Production environment.</li><li>Minimum of 3 years supervisory experience.</li><li>Must have working knowledge of HACCP, GMPs, quality systems, and experience working with and leading team in a manufacturing environment.</li><li>Must possess understanding of FDA and local regulatory requirements.</li></ul><p>OTHER SKILLS</p><ul><li>Must be hold all applicable food safety certifications (SQF Practitioner, HACCP, PCQI, etc...).</li><li>Effective management and supervisory skills.</li><li>Must have excellent facilitating skills in a team environment, and effective communication skills, both written and oral.</li><li>Training skills with ability to develop own curriculum.</li><li>Must be a demonstrated problem solver with the ability to implement effective solutions.</li><li>Working knowledge of statistical and other advanced analytical problem-solving tools.</li><li>Must be able to read, write and communicate in the English language.</li></ul><p><b>Physical Requirements: </b></p><ul><li>Must be able to lift, pull and push 50 pounds and stand for entire 8-hour shift</li><li>Must be able to bend, reach, stoop and squat</li><li>Must be able to work in a highly pollenated environment (kief)</li><li>Must be able to work in hot and humid weather conditions.</li></ul><p><b>Why You’d Love This Role</b></p><p>You have:</p><ul><li>A high level of professionalism and believe in our founding principles: “Cannabis for humanity” and “Change for the better”. As such, you enjoy being involved in the community and being a steward for the company and the positive change that we believe in.</li><li>A passion for providing the residents and visitors of Michigan with the highest quality and safest cannabis products in the state.</li><li>A desire to change the social perception of cannabis and a passion for humanity.</li><li>A constant desire to learn new skills and believe in continuous improvement, both personally and professionally.</li><li>Value integrity and honesty and want to bring those values to the cannabis industry.</li><li>Enjoy being part of a team and sharing your skills with your fellow citizens.</li><li>An appreciation for all stages of the production cycle of cannabis, including harvesting and trimming.</li><li>An awareness of the contamination risk between a commercial and home grow, and thus can commit to not operating a home grow while working with us in the greenhouse</li></ul><p><b>Common Citizen</b> is an equal opportunity employer. We celebrate diversity and are committed to creating an environment of mutual respect for all people. If you are a member of an equity group, you are encouraged to self-identify, on your application, cover letter or resume.</p><p><b>***Must be at least 21 years of age as required by the Marijuana Regulatory Association***</b></p><p>Job Type: Full-time</p><p>Benefits:</p><ul><li>Dental insurance</li><li>Health insurance</li><li>Paid time off</li></ul><p>Schedule:</p><ul><li>8 hour shift</li></ul><p>Education:</p><ul><li>Bachelor's (Preferred)</li></ul><p>Experience:</p><ul><li>Quality Assurance: 3 years (Preferred)</li><li>Food Manufacturing: 3 years (Preferred)</li></ul><p>Work Location:</p><ul><li>One location</li></ul><p>Work Remotely:</p><ul><li>No</li></ul></div>","company":{"companyType":"Private/Established","name":"Common Citizen","logoUrl":"/logos/common-citizen-3e62d75f14959e7a96405c11214563de.png"},"location":{"country":"United States","address":"Marshall, MI 49068","city":"Marshall","stateProvince":"MI"},"frontendLink":"/job-posting/common-citizen/quality-assurance-administrator/623f1fd348ea8b6f063b7c37327a90c0","title":"Quality Assurance Administrator","hash":"623f1fd348ea8b6f063b7c37327a90c0","postingUrl":"https://www.indeed.com/job/quality-assurance-administrator-e383d34c3637e3e8"},{"employmentType":"Full-time","postedOn":"2 days ago","description":"<div><p>Quality Assurance TechnicianDescriptionJob Title: Quality Assurance TechnicianDepartment: Quality Assurance- CultivationReports to: Quality Assurance Supervisor- CultivationFLSA Status: FT - Non-ExemptLocation: Monticello, FLRole Summary: The Quality Assurance Tech-Cultivation is responsible for conducting scans on trimmed product in effort to assure quality and safety of products intended for consumers. QA Techs will be responsible for tracking the weight of each sample and keeping track of what cultivar is currently being worked on. Additionally, QA Techs will be required to safely handle and separate any adulterated product that is found during scans.Key Duties and Responsibilities:Conduct visual inspections of cannabis for organic and inorganic adulterants and defects.Document inspection results by completing reports and logs and inputting data into quality database.Keep equipment (i.e. scales, tools, etc) in good, working order.Maintain a safe and healthy work environment by following departmental standard operating procedures (SOPs), adhering to cGMP SOPs, and complying with legal regulationsMaintains and ensures that proper PPE is utilized and changed out regularly, or as neededProvide Feedback as neededPerforms other duties as requiredPosition RequirementsSKILLS AND QUALIFICATIONSHigh School Diploma/GED or equivalent educationDetail OrientedCoachable and a willingness to learnAbility to work in a fast-paced environmentAbility to focus and avoid distractionsComfortable operating digital scalesBasic computer knowledgeBasic math and reading comprehensionOrganizational skillsADDITIONAL MINIMUM QUALIFICATIONSMust be able to move intermittently throughout the workday. Due to the nature of our business, it is advocated that when representing Trulieve that our professionalism meets the needs of the medical patient base that we respectively serve. To uniformly align with the organization, an individual must be able to provide a level of communication that aligns respectively with the diversification of our patients which may exhibit opportunities to assess the situation and apply meaningful service. In addition, must be able to quickly identify and insert additional support where needed to deescalate situations without compromising Trulieve's objective in serving our patient base with excellent customer service.Must be able to push, pull, move, and/or lift a minimum of 25 pounds to a minimum height of 5 feet and be able to push, pull, move, and/or carry such weight a minimum distance of 50 feet, with or without mechanical assistance.WORK SCHEDULE:45+ hours weekly with flexible hours depending on business needs. Must be available to work occasional evenings, weekends and holidays. 1st shift hours: 7am-4pm. 2nd shift hours: 2pm-11pmEqual Opportunity Employer l Trulieve Supports a Drug Free WorkplaceFull-Time/Part-TimeFull-Time ShiftVarious Shifts Level 2 Background check requiredPositionQuality Assurance Technician DivisionTrulieve, INC Close DatePost Internal Days0 Number of Openings2 Number Filled0 Exempt/Non-ExemptNon-Exempt Req NumberCUL-21-00090 Open Date4/5/2021 LocationMonticello EOE StatementWe are an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status or any other characteristic protected by law. This position is currently accepting applications</p></div>","company":{"website":"trulieve.com","companyType":"Public/Established","name":"Trulieve Cannabis","logoUrl":"/logos/trulieve-1d76a294c42e35e1fad949d6f74742d9.png"},"location":{"country":"United States","address":"Monticello, FL, USA","city":"Monticello","stateProvince":"FL"},"frontendLink":"/job-posting/trulieve-cannabis/quality-assurance-technician/f0ec3ef5213609620590248535ecdd2f","title":"Quality Assurance Technician","hash":"f0ec3ef5213609620590248535ecdd2f","postingUrl":"https://www.topjob4me.com/job/quality-assurance-technician-in-monticello-florida/6492-1198684833A1"},{"employmentType":"Full-time, Permanent","postedOn":"3 days ago","description":"<div><p>The Quality Assurance Associate will report to the Quality Assurance Manager (QAP) or Alternate QAP in lieu and designated management as required. The Quality Assurance Associate is responsible for supporting the Quality Assurance initiatives within the department to ensure that cannabis products produced meet the organization’s objectives for quality, safety, regulatory and customer expectations in accordance with the Cannabis Act and Regulations in accordance with Health Canada guidelines.</p><p><b>ABOUT US: </b></p><p>BZAM is as awesome as it sounds! We are an integrated cannabis company whose mission and brand stand for quality and integrity. Our commitment to excellence, service and employee satisfaction is demonstrated in our agile and strategic approach to market entry and investment in our people. As an emerging company in a rapid growth industry, BZAM’s innovative and accomplished leadership team is the cornerstone of our business and portfolio development.</p><p><b>YOUR </b><b>CONTRIBUTION: </b></p><p>Ø Support the Quality Assurance Department in implementing SOPs &amp; Quality Management Programs and projects to ensure GPP compliance under the Cannabis Act/Regulations; work cross-departmentally to implement SOPs (i.e. Operations, Regulatory, Security);</p><p>Ø Assist in implementation of training programs around SOPs pertaining to GPP and Record Keeping Compliance; collaborate training programs with Human Resources and assess training gaps continuously;</p><p>Ø Support the QA Department’s quality programs/systems for cannabis storage;</p><p>Ø Assist in the implementation of programs around GPP &amp; Record Keeping Methods for sanitation of premises, equipment, cleanliness, hygienic behaviour of personnel, and facility maintenance;</p><p>Ø Collaborate with Regulatory and Security Departments to develop and perform internal audits regularly to determine quality assurance compliance according to Cannabis Regulations;</p><p>Ø Maintain current knowledge of best practices for the provisions of the Cannabis Act and Cannabis Regulations that apply to the license holder; and</p><p>Ø Other duties as assigned.</p><p><b>WHAT YOU BRING: </b></p><p>Ø BSc. in Chemistry, Biology, Pharmacology or Food Science, obtained or recognized by a Canadian University;</p><p>Ø 3+ years’ professional experience in Quality Assurance/Control in a production environment;</p><p>Ø Preferred knowledge of plant chemistry, extraction and formulation systems, and chromatographic techniques;</p><p>Ø Recent criminal record check completed (required prior to hiring);</p><p>Ø Solid ERP, MS Office Suite, Adobe Pro, G-Suite and additional technical proficiency; and</p><p>Ø Valid security clearance (ACMPR or Cannabis Regulations).</p><p>You Are FOCUSED, DETAIL ORIENTED, AND METHODICAL. Nothing gets by you and you are a master at time management.</p><p>You are a CLEAR COMMUNICATOR capable of speaking and writing professionally, clearly and concisely.</p><p>You are a RESEARCH GURU, proficient in researching and retaining complicated compliance knowledge.</p><p>You are ORGANIZED and strongly skilled in the area of project management.</p><p><b>YOUR EXPERIENCE: </b></p><p>Ø Proven knowledge and demonstrable experience in the stated responsibilities of the position (i.e. Food, Pharma, NHP);</p><p>Ø Experience in creating and supporting process enhancement initiatives to maintain an environment of continuous learning and improvement;</p><p>Ø Preferred experience with cGMP, GAP, GLP, HACCP, ISO and FDA;</p><p>Ø Preferred experience with design inspection methods, fabrication and production of medical cannabis; and</p><p>Ø Experience working with technical reports, hazard critical control analysis, and inspecting production resources and materials.</p><p><b>WHAT WE OFFER: </b></p><p>Ø Competitive Compensation and Benefits Package</p><p>Ø Rapid growth and advancement potential</p><p>Ø Learning and development opportunities</p><p>Ø Dynamic and innovative environment</p><p>Ø Exceptional culture</p><p><b><i>BZAM is an Equal Employment Opportunity employer that values the strength of diversity within the workplace. All qualified applicants, regardless of race, colour, religion, gender, sexual orientation, marital status, gender identity or expression, nationality, age, disability or veteran status, or any other characteristic protected by applicable law, are strongly encouraged to apply.</i></b></p><p>Job Types: Full-time, Permanent</p><p>Benefits:</p><ul><li>Dental care</li><li>Extended health care</li><li>RRSP match</li><li>Vision care</li></ul><p>COVID-19 considerations:<br />BZAM Cannabis is committed to following all provincial and federal public health authority guidance pertaining to COVID-19</p><p>Education:</p><ul><li>Bachelor's Degree (preferred)</li></ul><p>Experience:</p><ul><li>Quality assurance or Quality Control: 3 years (preferred)</li><li>cGMP, GAP, GLP, HACCP, ISO and FDA: 2 years (preferred)</li></ul></div>","company":{"companyType":"Private/Established","name":"BZAM Management Inc.","logoUrl":"/logos/bzam-cannabis-b38c86b85c95534fc19e12da77b862d5.jpeg"},"location":{"country":"Canada","address":"Pitt Meadows, BC","city":"Pitt Meadows","stateProvince":"BC"},"frontendLink":"/job-posting/bzam-management-inc/quality-assurance-associate/06f2c6939aede892381936d3bd87e59a","title":"Quality Assurance Associate","hash":"06f2c6939aede892381936d3bd87e59a","postingUrl":"https://ca.indeed.com/job/quality-assurance-associate-042b15d9167d1bf3"},{"employmentType":"Full-time","postedOn":"5 days ago","description":"<div><p>Quality Assurance Manager Job at High Park Company – London, ON</p><p>Quality Assurance Manager – London, Ontario</p><p>NOTE TO APPLICANTS: Preference will be given to candidates with cannabis, food manufacturing and/or CPG manufacturing experience.</p><p>Reporting to the VP, Quality, the Quality Assurance Manager will be responsible for the coordination of work to ensure the successful implementation of High Park Holdings, Ltd. quality management system in pursuance of regulatory compliance and achievement of business goals. The Quality Assurance Manager will work closely with production, maintenance, facilities and shipping teams to ensure that quality standards are established, implemented and maintained throughout all manufacturing operations.</p><p>Through the effective management of targets, goals and production efficiencies, the Quality Assurance Manager will ensure the ongoing success of the Quality Assurance team. The Quality Assurance Manager will improve quality inspection, monitoring documentation and other in-house processes with the objective of constant improvement of quality processes. The Quality Assurance Manager will support the development, implementation and ongoing monitoring of the quality assurance systems in strict compliance with the Cannabis Act and Cannabis Regulations.</p><p>Role and Responsibilities</p><p>• Oversee High Park London Quality Assurance department as per the Cannabis Act and Cannabis Regulations pertaining to production, processing, packaging, labeling in compliance with Good Production Practices</p><p>• Establish and enforce Good Production Practices (GPP), Good Documentation Practices (GDP), Good Agricultural Practices (GAP), and Quality Assurance standards</p><p>• Support continuous quality improvement of High Park London cannabis manufacturing through reinforcement of product quality programs, creation of specifications, and performance and oversight of various auditing and investigation actions</p><p>• Prepare and maintain batch records; manage batch approval and release process, including final review and batch approval</p><p>• Review regulations, documents and reports pertaining to the Cannabis Act and Cannabis Regulations.</p><p>• Participate in Health Canada inspections</p><p>• Ensure compliance with regulations through internal auditing and quality systems</p><p>• Manage and be accountable for a team of Quality Assurance staff</p><p>• Interact with production and department managers to manage a well-run quality assurance program</p><p>• Review of Quality Control documents, test results, certificates of analysis, procedures and production equipment to ensure compliance to specification</p><p>• Oversee preparation of Deviation Investigation Reports, including Root Cause Analysis and Corrective and Preventative Action plans</p><p>• Manage procedures and processes pertaining to change control, incidents, complaints, deviations and recalls</p><p>• Monitor the performance of quality assurance employees within department</p><p>• Oversee the site IQ/OQ/PQ program for equipment and processes</p><p>• Responsible for the investigation of all product related complaints</p><p>• Resolve work problems and recommend measures to improve productivity and product quality</p><p>• Motivate members through the setting of clear expectations</p><p>• Coordinate with other supervisors, leads, and managers to obtain maximum use of resources</p><p>• Plan for manpower and equipment needs</p><p>• Ensure compliance with company standards for cost control, waste reduction, quality, safety, and complete and on-time delivery</p><p>• Provide leadership for problem and conflict resolution</p><p>• Identify and determine quality and productivity related problems and solutions</p><p>• Coordinate and oversee employee work assignments and special projects</p><p>• Maintain and adhere to all company policies and procedures</p><p>• Perform other tasks as may be assigned</p><p>Qualifications and Education Requirements</p><p>• Bachelor’s degree in a technical discipline (Food, Physical, or Biological Sciences preferred)</p><p>• 3+ years of experience as a Quality Manager or Supervisor in a GPP, GMP and/or HACCP regulated environment required</p><p>• Strong leadership and communication skills</p><p>• Direct experience participating in, managing, or conducting quality audits and inspections</p><p>• Strong and current knowledge of Good Production Practice, Good Documentation Practice</p><p>• Familiarity with the Cannabis Act and Cannabis Regulations</p><p>• Proficiency quality management systems, documentation, testing methods</p><p>• Experience establishing and maintaining version-controlled standards, policies, procedures and work flows</p><p>• Proficient understanding of plant products and related test methodology is an asset</p><p>• Chemistry and Plant Biology knowledge is an asset</p><p>• Proven ability to effectively use Microsoft Office Applications</p><p>• Must have the ability to obtain security clearance status under the Cannabis act and Cannabis Regulations</p><p>High Park Company was established to develop, sell, and distribute inspiring and iconic adult-use cannabis brands. High Park Company is a wholly-owned subsidiary of Tilray, a global leader in cannabis cultivation, processing, and distribution. Tilray serves patients in Canada and around the world with a diverse range of pharmaceutical-grade medical cannabis products as High Park Company focuses on creating distinctive products for adult Canadian consumers.</p><p>High Park welcomes applications from all qualified individuals and is committed to employment equity and diversity in the workplace.</p><p>Accommodations are available for applicants with disabilities throughout the recruitment process. If you require accommodations for interviews or other meetings, please advise when submitting your application.</p><p>Please note that High Park does not authorize, engage, or sponsor any consultants, agencies or organizations that seek certain personal or financial information from you (e.g. passwords, login ids, credit card information). High Park does not charge any application, processing or onboarding fee at any stage of the recruitment or hiring process.</p><p>Job Types: Full-time, Permanent</p><p><b>Additional pay:</b></p><p><b>Benefits:</b></p><p>• Casual dress</p><p>• Dental care</p><p>• Disability insurance</p><p>• Employee assistance program</p><p>• Extended health care</p><p>• Life insurance</p><p>• On-site parking</p><p>• RRSP match</p><p><b>Schedule:</b></p><p><b>Education:</b></p><p>• Bachelor’s Degree (preferred)</p><p><b>Experience:</b></p><p>• GMP: 1 year (preferred)</p><p>• Quality Assurance leadership: 3 years (required)</p><p>• cannabis, food manufacturing or CPG: 1 year (required)</p><p><b>Work remotely:</b></p><p>About the Company</p><p>Company: High Park Company –</p><p>Company Location: London, ON</p><p>Estimated Salary</p></div>","company":{"website":"highparkcompany.com","companyType":"Public/Established","name":"High Park Company","logoUrl":"/logos/high-park-company-c3260afcfbbc534766eac49502ad321a.jpeg"},"location":{"country":"Canada","address":"Toronto, ON (+1 other)","city":"Toronto","stateProvince":"ON"},"frontendLink":"/job-posting/high-park-company/quality-assurance-manager/5c603e30ed71807e3c2ade98dd5d553d","title":"Quality Assurance Manager","hash":"5c603e30ed71807e3c2ade98dd5d553d","postingUrl":"https://qajobshub.com/job/quality-assurance-manager-296/"},{"employmentType":"Full-time","postedOn":"6 days ago","description":"<div><p>Quality Assurance Manager Job at High Park Company – London, ON</p><p>Quality Assurance Manager – London, Ontario</p><p>NOTE TO APPLICANTS: Preference will be given to candidates with cannabis, food manufacturing and/or CPG manufacturing experience.</p><p>Reporting to the VP, Quality, the Quality Assurance Manager will be responsible for the coordination of work to ensure the successful implementation of High Park Holdings, Ltd. quality management system in pursuance of regulatory compliance and achievement of business goals. The Quality Assurance Manager will work closely with production, maintenance, facilities and shipping teams to ensure that quality standards are established, implemented and maintained throughout all manufacturing operations.</p><p>Through the effective management of targets, goals and production efficiencies, the Quality Assurance Manager will ensure the ongoing success of the Quality Assurance team. The Quality Assurance Manager will improve quality inspection, monitoring documentation and other in-house processes with the objective of constant improvement of quality processes. The Quality Assurance Manager will support the development, implementation and ongoing monitoring of the quality assurance systems in strict compliance with the Cannabis Act and Cannabis Regulations.</p><p>Role and Responsibilities</p><p>• Oversee High Park London Quality Assurance department as per the Cannabis Act and Cannabis Regulations pertaining to production, processing, packaging, labeling in compliance with Good Production Practices</p><p>• Establish and enforce Good Production Practices (GPP), Good Documentation Practices (GDP), Good Agricultural Practices (GAP), and Quality Assurance standards</p><p>• Support continuous quality improvement of High Park London cannabis manufacturing through reinforcement of product quality programs, creation of specifications, and performance and oversight of various auditing and investigation actions</p><p>• Prepare and maintain batch records; manage batch approval and release process, including final review and batch approval</p><p>• Review regulations, documents and reports pertaining to the Cannabis Act and Cannabis Regulations.</p><p>• Participate in Health Canada inspections</p><p>• Ensure compliance with regulations through internal auditing and quality systems</p><p>• Manage and be accountable for a team of Quality Assurance staff</p><p>• Interact with production and department managers to manage a well-run quality assurance program</p><p>• Review of Quality Control documents, test results, certificates of analysis, procedures and production equipment to ensure compliance to specification</p><p>• Oversee preparation of Deviation Investigation Reports, including Root Cause Analysis and Corrective and Preventative Action plans</p><p>• Manage procedures and processes pertaining to change control, incidents, complaints, deviations and recalls</p><p>• Monitor the performance of quality assurance employees within department</p><p>• Oversee the site IQ/OQ/PQ program for equipment and processes</p><p>• Responsible for the investigation of all product related complaints</p><p>• Resolve work problems and recommend measures to improve productivity and product quality</p><p>• Motivate members through the setting of clear expectations</p><p>• Coordinate with other supervisors, leads, and managers to obtain maximum use of resources</p><p>• Plan for manpower and equipment needs</p><p>• Ensure compliance with company standards for cost control, waste reduction, quality, safety, and complete and on-time delivery</p><p>• Provide leadership for problem and conflict resolution</p><p>• Identify and determine quality and productivity related problems and solutions</p><p>• Coordinate and oversee employee work assignments and special projects</p><p>• Maintain and adhere to all company policies and procedures</p><p>• Perform other tasks as may be assigned</p><p>Qualifications and Education Requirements</p><p>• Bachelor’s degree in a technical discipline (Food, Physical, or Biological Sciences preferred)</p><p>• 3+ years of experience as a Quality Manager or Supervisor in a GPP, GMP and/or HACCP regulated environment required</p><p>• Strong leadership and communication skills</p><p>• Direct experience participating in, managing, or conducting quality audits and inspections</p><p>• Strong and current knowledge of Good Production Practice, Good Documentation Practice</p><p>• Familiarity with the Cannabis Act and Cannabis Regulations</p><p>• Proficiency quality management systems, documentation, testing methods</p><p>• Experience establishing and maintaining version-controlled standards, policies, procedures and work flows</p><p>• Proficient understanding of plant products and related test methodology is an asset</p><p>• Chemistry and Plant Biology knowledge is an asset</p><p>• Proven ability to effectively use Microsoft Office Applications</p><p>• Must have the ability to obtain security clearance status under the Cannabis act and Cannabis Regulations</p><p>High Park Company was established to develop, sell, and distribute inspiring and iconic adult-use cannabis brands. High Park Company is a wholly-owned subsidiary of Tilray, a global leader in cannabis cultivation, processing, and distribution. Tilray serves patients in Canada and around the world with a diverse range of pharmaceutical-grade medical cannabis products as High Park Company focuses on creating distinctive products for adult Canadian consumers.</p><p>High Park welcomes applications from all qualified individuals and is committed to employment equity and diversity in the workplace.</p><p>Accommodations are available for applicants with disabilities throughout the recruitment process. If you require accommodations for interviews or other meetings, please advise when submitting your application.</p><p>Please note that High Park does not authorize, engage, or sponsor any consultants, agencies or organizations that seek certain personal or financial information from you (e.g. passwords, login ids, credit card information). High Park does not charge any application, processing or onboarding fee at any stage of the recruitment or hiring process.</p><p>Job Types: Full-time, Permanent</p><p><b>Additional pay:</b></p><p><b>Benefits:</b></p><p>• Casual dress</p><p>• Dental care</p><p>• Disability insurance</p><p>• Employee assistance program</p><p>• Extended health care</p><p>• Life insurance</p><p>• On-site parking</p><p>• RRSP match</p><p><b>Schedule:</b></p><p><b>Education:</b></p><p>• Bachelor’s Degree (preferred)</p><p><b>Experience:</b></p><p>• GMP: 1 year (preferred)</p><p>• Quality Assurance leadership: 3 years (required)</p><p>• cannabis, food manufacturing or CPG: 1 year (required)</p><p><b>Work remotely:</b></p><p>About the Company</p><p>Company: High Park Company –</p><p>Company Location: London, ON</p><p>Estimated Salary</p></div>","company":{"website":"highparkcompany.com","companyType":"Public/Established","name":"High Park Company","logoUrl":"/logos/high-park-company-c3260afcfbbc534766eac49502ad321a.jpeg"},"location":{"country":"Canada","address":"London, ON","city":"London","stateProvince":"ON"},"frontendLink":"/job-posting/high-park-company/quality-assurance-manager/e33abdeb5411e35924a815066d71011c","title":"Quality Assurance Manager","hash":"e33abdeb5411e35924a815066d71011c","postingUrl":"https://pharmajobs.me/job/quality-assurance-manager-4/"},{"postedOn":"4 days ago","description":"<div><div><p>Aqualitas Inc. is a licensed medical cannabis producer, with our corporate Head Office located in Bedford, Nova Scotia, and our Production Facility located on the South Shore of Nova Scotia in the Region of Queens Municipality. We are committed to quality, sustainability and balance; in our products, our operations and our people.</p><p></p><p><b><br />QUALITY ASSURANCE TECHNICIAN- ONE YEAR TERM</b></p><p></p><p><br />We are currently seeking a skilled QA Technician at our production facility located in <b><i>Brooklyn, Queens County, NS</i></b>. Reporting to the QA Manager, you will actively contribute to and support the day-to-day efforts of the QA/QC Team across all departments at the facility.</p><p></p><p><b><br />Responsibilities include, but are not limited to</b><b>:</b></p><p></p><ul><li><br />Maintaining operations by strictly adhering at all times to company, industry and regulatory Policies, Standard Operating Procedures (SOPs), Work Instructions (WIs), Good Production Practices (GPP), Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), and reporting any required changes.</li><li>Maintaining databases by entering new analytical results and QC testing data</li><li>Creating Quality Dashboard and Quality Scorecard for Executive Team review when needed</li><li>Collecting, entering and analyzing data from, as well as inspecting and monitoring as required for, various departments (Packaging, Sanitation, Aquaponics, Cultivation), including:<ul><li>Packaging re-work data</li><li>Finished product inspection</li><li>Trim Room monitoring</li><li>Drying sample collection and monitoring</li><li>Water analysis</li><li>AQL In-process Inspection</li><li>Excise stamp and shipping inspection</li></ul></li><li>Reviewing data for deficiencies and working towards continuous methods to improve data management</li><li>Resolving deficiencies by following SOPs and consulting with QA Manager/QAP regarding incomplete documentation</li><li>Securing information by completing database backups in consultation with IT Technician</li><li>Providing appropriate documents to Post-Production team when needed</li><li>Additional QA tasks as required, including:<ul><li>Packaging Room QA backup</li><li>Training staff on activities and deviations noted in the process</li><li>Conducting line clearances</li><li>Conducting swabbing on rooms and equipment</li></ul></li><li>Maintaining strict confidentiality at all times to protect operations and ensure customer confidence</li><li>Finished product Inspection</li><li>Documents Provided to Post production Team</li><li>Excise Stamps inspection / Shipping Inspection</li><li>Trim room monitoring</li><li>Site audit activities</li><li>Status Labelling</li><li>Drying Sample collection and Monitoring</li><li>Cover other QA shift when required</li><li>Other duties as may be assigned from time to time</li></ul><p></p><p><b><br />Qualifications</b><b>:</b></p><ul><li>Bachelor of Science in Chemistry, Biology or Environmental Science or related manufacturing experience</li><li>Understanding sound quality assurance principles, statistical process control, sanitation</li><li>Familiarity with pH meter and moisture analyzers, micro swabbing and calibration of equipment</li><li>Good understanding of GPP/EU-GMP, HACCP</li><li>Experience with GPP/GMP Standards</li></ul><p></p><p><b><br />Skills</b><b>:</b></p><ul><li>Accurate and efficient keyboarding and data entry skills</li><li>Advanced knowledge of Excel software</li><li>Keen recordkeeping, editing and documentation abilities</li><li>Superior time management and organizational abilities to establish entry and daily task priorities</li><li>Comfort level working in groups or individually</li><li>Comfort level of working with groups to collaborate and communicate</li><li>Self directed to know the needed schedule day to day</li></ul><p></p><p><b><br />Other details</b><b>:</b></p><p><i>Location</i>: Brooklyn, NS (Required); occasional travel to Bedford/HRM area may be possible</p><p><i>Compensation</i>: To be determined based on skills and experience</p><p><i>Status and Hours</i>: One year Term, Full-Time (40 hrs/week)</p><p></p><p><b><i><br />Successful applicants must provide satisfactory background and reference checks.</i></b></p><p></p><p><br />Aqualitas welcomes and encourages diversity. Should you require an accommodation in any aspect of our selection process, please let us know.</p><p></p><p><br />We appreciate the interest of all candidates; however, we will only be contacting those that best fit our requirements. Resumes will be kept for consideration for six months.</p></div></div>","company":{"companyType":"Private/Growth","name":"Aqualitas Inc.","logoUrl":"/logos/aqualitas-3e7851baa3715671eadbf19c677e9a3a.jpeg"},"location":{"country":"Canada","address":"Brooklyn, NS","city":"Brooklyn","stateProvince":"NS"},"frontendLink":"/job-posting/aqualitas-inc/quality-assurance-technician/abf728e1323c0d61d2f2e4dad8edfb4f","title":"Quality Assurance Technician","hash":"abf728e1323c0d61d2f2e4dad8edfb4f","postingUrl":"https://ca.indeed.com/job/quality-assurance-technician-2db6895971d1c2e8"},{"employmentType":"Full-time, Permanent","postedOn":"4 days ago","description":"<div><p><b>Position: </b> Quality Assurance Technician<br /><b>Reporting To: </b> QA Manager<br /><b>Location: </b> Calgary, AB<br /><b>Type: </b> Full Time, Permanent</p><p><b>The Position</b></p><p>OGEN is looking for a highly motivated and detail-oriented individual to join our growing team! The Quality Assurance Technician is an entry-level position that is responsible for the daily administrative duties of the department. The ideal candidate is organized, communicative, proficient with computer applications, and adaptable. This high-volume position requires the ability to work under pressure in a fast-paced environment with competing deadlines and priorities.</p><p><b>About OGEN LTD.</b></p><p>OGEN LTD. is a licensed producer located in Calgary, Alberta. We cultivate small-batch, craft cannabis to deliver a high-end, dried flower product of exceptional quality. We work as a team and are proud to grow in a world-class indoor hydroponic facility.</p><p><b>Position Duties and Responsibilities</b></p><p>Reporting to the Quality Assurance Manager, the selected candidate’s duties and responsibilities will include the following:</p><p>· Assist in filing, records review, distribution, archival, logbooks, and all required follow-up</p><p>· Perform label control process: preparation, counting, inventory, issuance, and destruction</p><p>· Assist with Production Work Order (PWO) documents: issuance and retrieval</p><p>· Review of Quality Control (QC) raw data results, and reports</p><p>· Coordination of sample shipments to laboratories</p><p>· Support the inspection of incoming materials and assist with material release</p><p>· Identify non-conformities and deviations and assist with investigations, as required</p><p>· Understand and follow SOPs and procedures to GMP/GPP standards</p><p>· Assist the QA Associate, QA Manager, and QA Director, as required</p><p><b>Minimum Requirements</b></p><p>· Successfully pass a criminal record check and other security-related requirements</p><p>· Must be legally entitled to work in Canada</p><p>· Must be 18 years of age or older</p><p>· Minimum of 1 year of experience working in Quality Control</p><p>· Completion of High School Diploma or equivalent</p><p>· Some post-secondary education in a related field</p><p>· Proficient in Microsoft Office suites and adept at learning new software programs</p><p><b>Soft Skills</b></p><p>· Must have good interpersonal skills to maintain effective work relationships</p><p>· Excellent written and verbal communication skills</p><p>· Highly organized and strong attention to detail skills</p><p>· Possess a high level of problem-solving abilities and remain calm in all situations</p><p><b>Position Preferences</b></p><p>· Experience in a cannabis, liquor, tobacco, pharmaceutical or other highly regulated industry</p><p>· Understanding of a Document Control System within a manufacturing environment</p><p>· Familiarity with GPP and/or GMP</p><p><b>Working Conditions and Physical Requirements </b></p><p>· Willingness to perform repetitive tasks</p><p>· Ability to work under high pressure in a fast-paced environment managing multiple priorities</p><p><b>How to Apply</b></p><p>If this position sounds like the right fit and opportunity for you, please submit a cover letter and resume for consideration. Your cover letter should address the following qualification questions:</p><ul><li>Would you successfully pass a criminal background check and security-related requirements?</li><li>What previous experience and skills would make you the ideal candidate for this role?</li><li>Why do you want to work for OGEN?</li><li>How did you hear about this position?</li></ul><p><b>Stay Connected to Us</b></p><p>Follow us on LinkedIn, Facebook, and Instagram for the latest news and job postings</p><p><b>Our Values</b></p><p><b>STREET: </b>we honour the pioneers before us. Without them, the landrace strains would be extinct and new hybrids would not exist. We follow in their footsteps, to maintain the art of cultivation.</p><p><b>SCIENCE: </b>we are forward thinkers, inspired by science, technology and data. We continuously improve our processes by hypothesizing, gathering data, and applying our knowledge. It helps us cultivate consistently and safely to meet the strict cannabis regulations.</p><p><b>QUALITY: </b>we are connoisseurs, not mass producers. We select the best genetics and we pheno-hunt. We take the time to hang-dry, hand-trim and slow cure our cannabis. Our expectations are high because we demand top quality for our customers and ourselves.</p><p><b>HUMILITY: </b>with every new challenge we find a better way, we push the boundaries and we don’t give up.</p><p><b>COMMUNITY: </b>we are proud to be local and we share the entrepreneurial spirit of Alberta. We believe in the craft movement, an appreciation of how things are carefully made.</p><p>Reference ID: QAT05122021WHW</p><p>Application deadline: 2021-06-16</p><p>Expected start date: 2021-05-31</p><p>Job Types: Full-time, Permanent</p><p>Benefits:</p><ul><li>Casual dress</li><li>Dental care</li><li>Extended health care</li><li>On-site parking</li><li>Paid time off</li></ul><p>Schedule:</p><ul><li>Day shift</li><li>Monday to Friday</li><li>Overtime</li></ul><p>Application question(s):</p><ul><li>What previous experience and skills would make you the ideal candidate for this role?</li><li>Would you successfully pass a criminal background check and security-related requirements?</li></ul><p>Education:</p><ul><li>Secondary School (required)</li></ul><p>Experience:</p><ul><li>Administrative experience: 1 year (required)</li><li>Manufacturing: 1 year (preferred)</li><li>Microsoft Office: 2 years (preferred)</li></ul><p>Work remotely:</p><ul><li>No</li></ul></div>","company":{"companyType":"Public/Growth","name":"OGEN LTD.","logoUrl":"/logos/ogen-ltd-edbcc55fff7e49bc7c001f74ae0d7ceb.jpeg"},"location":{"country":"Canada","address":"Calgary, AB","city":"Calgary","stateProvince":"AB"},"frontendLink":"/job-posting/ogen-ltd/quality-assurance-technician/35a611487da46f8c8924ca06b02c2dc8","title":"Quality Assurance Technician","hash":"35a611487da46f8c8924ca06b02c2dc8","postingUrl":"https://ca.indeed.com/job/quality-assurance-technician-4da557ecf5b9c140"},{"employmentType":"Full-time","postedOn":"5 days ago","description":"<div><p><b>Job Description</b></p><p><b>Quality Assurance Technician</b></p><p>Location: Jacksonville, FL</p><p>As a Quality Assurance (QA) Technician, you will be responsible for assisting with quality-related activities including start-up verification, in-process verification &amp; checks, BMR and documentation reviews, sampling, and inspection of finished products. Products include cannabis flower, cannabis oil, infused products (concentrates, capsules, lotions, tinctures, vapes, etc.) and food products (chocolate, gummies, lozenges, etc.). This position will also help ensure products are being produced in a manner that meets all specifications and brand consistency. You will also assist in identifying potential quality risks and working with operations personnel to develop improvement opportunities. The ideal candidate must possess a strong attention to detail and experience working within a highly regulated industry.</p><p><b>Job Summary and Responsibilities</b>:</p><p>- Performs finished product sampling and inspection</p><p>- Performs equipment and product line clearances before production runs</p><p>- Performs in-process verification to ensure product weights, correct labeling &amp; packaging</p><p>- Performs verification on finished products</p><p>- Inspects retain samples and customer return samples, as deemed necessary</p><p>- Assists in customer complaints and product investigations, helping to assess risk, identify root cause and quarantine product</p><p>- Inspects packaged orders to ensure correct content and quantities, as deemed necessary</p><p>- Reviews in-process batch documentation to ensure real-time compliance to product specifications, good documentation practices and written policies/procedures</p><p>- Monitors compliance to established Good Manufacturing Practice (GMP) and Safe Quality Foods guidance</p><p>- Conducts all duties in compliance with safety rules, applicable SOPs, and other applicable guidelines</p><p>- May require travel to other states or facilities to assist with inspections or quality issues</p><p><b>Required Experience, Education and Skills: </b></p><p>- Bachelors Degree, 1-3 years’ experience or Associate Degree, 5+ years’ experience</p><p>- Prior experience in highly regulated industry. Highly desirable: healthcare, medical devices, pharmaceutical, consumer packaged goods (food), cannabis. Highly desirable: FDA, HACCP, SQF experience</p><p>- Prior experience in Quality Assurance or Quality Control function</p><p>- Prior experience with product sampling, inspection procedures, customer complaints, product investigations, and CAPA</p><p>- Ability to follow written procedures and monitor others for adherence to written procedures</p><p>- Ability to create or update written procedures with site operations personnel</p><p>- Strong written and verbal communication skills</p><p>- Detail-oriented</p><p>- Utilizes critical thinking to troubleshoot issues, work collaboratively with a team to brainstorm solutions, and implement improvement solutions</p><p>- Must be flexible and able to work long hours and weekends as required</p><p>- Able to adapt in a quick and positive manner</p><p>- Able to work in a fast-paced environment and handle multiple tasks and requests</p><p><b>Additional Requirements</b>:</p><p>- Must be 21 years of age or older</p><p>- Must comply with all legal and company regulations for working in the industry</p><p>- Ability to stand throughout extended periods, must be capable of squatting, standing, kneeling, bending, or walking throughout the workday</p><p>- Excellent communication skills and leadership both verbally and through written media.</p><p>- Strong decision-making, analytical and organizational skills</p><p>- Thorough understanding of state and local medical marijuana laws and how they apply to the operations</p><p><b>Physical Demands: </b></p><p>The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.</p><p>While performing the duties of this Job, the employee is regularly required to stand for extended periods every day. The employee must regularly lift and /or move up to 25 pounds, frequently lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus. Able to work 6 days a week and evening shifts if required.</p><p><b>Work Environment: </b></p><p>While performing the duties of this job, the employee will be standing indoors and frequently exposed to laboratory conditions. The employee is frequently exposed to fumes or airborne particles; toxic or caustic chemicals; and varying temperatures. The noise level in the work environment is usually loud.</p><p>Job Type: Full-time</p><p>Job Type: Full-time</p><p>Benefits:</p><ul><li>Dental insurance</li><li>Employee discount</li><li>Health insurance</li><li>Paid time off</li><li>Vision insurance</li></ul><p>Schedule:</p><ul><li>8 hour shift</li><li>Monday to Friday</li></ul><p>COVID-19 considerations:<br />All employees are required to wear a mask</p><p>Experience:</p><ul><li>Quality control: 1 year (Required)</li></ul><p>Work Location:</p><ul><li>One location</li></ul><p>Work Remotely:</p><ul><li>No</li></ul></div>","company":{"companyType":"Private/Established","name":"VidaCann","logoUrl":"/logos/vidacann-d27624162f7a910e07f93f882426ed6c.jpeg"},"location":{"country":"United States","address":"Jacksonville, FL 32216","city":"Jacksonville","stateProvince":"FL"},"frontendLink":"/job-posting/vidacann/quality-assurance-technician/cdcc1f2170e4962f05ed1f46f739648a","title":"Quality Assurance Technician","hash":"cdcc1f2170e4962f05ed1f46f739648a","postingUrl":"https://www.indeed.com/job/quality-assurance-technician-87c73aa8e0a8b69d"},{"employmentType":"Full-time","postedOn":"6 days ago","description":"<div><p>As a top Las Vegas dispensary, Planet 13 strives to provide the best quality recreational cannabis, cannabis extracts, and infused products available at competitive prices and with compassion that can only come from those who are knowledgeable in the field.</p><p>We are expanding in the Orange County area and are excited to be opening a new store this summer!</p><p><b>Summary</b></p><p>Assists in essential responsibilities of the inventory department and ensures state compliance standards and Planet 13 standards are met by preforming the following duties. Conducting daily audits of inventory, tracking and distribution of product. Accounting and reporting of inventory surplus and deficits complying with any State, City and MED requirements.</p><p>Essential Duties and Responsibilities include the following. Other duties may be assigned.</p><p>Conduct weekly/monthly physical inventory counts within the facility.</p><p>Complete inventory procedure using electronic tracking system (Biotrack) and respond to any discrepancies by notifying management and investigating reasons for the discrepancy.</p><p>Review inventory in Biotrack and METRC systems to ensure accuracy and compliance.</p><p>Responsible for the settlement of all inventory discrepancies and reporting the resolution of such discrepancies.</p><p>Manages and maintains compliance with METRC, ensures METRC inventory is up to date with POS system.</p><p>Coordinate with the management team to discuss inventory plans and methods to reduce errors and maximize inventory efficiency.</p><p>Participate in Quarterly/Yearly Audits.</p><p>Comply with inventory control procedures.</p><p>Supervisory Responsibilities</p><p>This job has no supervisory responsibilities.</p><p>Qualifications to perform this job successfully, an individual must be able to perform each essential duty 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 essential functions.</p><p><b>Education and/or Experience</b></p><p>High school diploma or general education degree (GED); or 6 to 12 months related experience and/or training; or equivalent combination of education and experience.</p><p><b>Language Skills</b></p><p>Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals. Ability to write routine reports and correspondence. Ability to speak effectively before groups of customers or employees of organization.</p><p>Mathematical Skills</p><p>Ability to add and subtract two-digit numbers and to multiply and divide with 10's and 100's. Ability to perform these operations using units of American money and weight measurement, volume, and distance.</p><p><b>Reasoning Ability</b></p><p>Ability to apply common sense understanding to carry out detailed but uninvolved written or oral instructions. Ability to deal with problems involving a few concrete variables in standardized situations.</p><p>Computer Skills</p><p>To perform this job successfully, an individual should have knowledge of Word Processing software, Inventory and Spreadsheet software.</p><p><b>Certificates, Licenses, Registrations</b></p><p>Must be able to possess a cannabis agent card and be 21 years of age or older.</p><p>Work Environment The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.</p><p>While performing the duties of this Job, the employee is occasionally exposed to extreme cold and extreme heat. The noise level in the work environment is usually moderate.</p><p>Disclaimer: Responsibilities and task outlined in this document are not exhaustive and may change as determined by the needs of the company.</p><p>Planet 13 values diversity in its workforce and is proud to be an AAP/EEO employer. All qualified applicants will receive consideration for employment without regard to race, sex, color, religion, sexual orientation, gender identity, national origin, age, protected veteran status, or on the basis of disability or any other legally protected class. The Company will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable federal, state and local laws. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process, or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Planet 13 Human Resources at [email protected]</p></div>","company":{"companyType":"Public/Established","name":"Planet 13","logoUrl":"/logos/planet-13-8461a4ff328184322170172f85bff04d.jpeg"},"location":{"country":"United States","address":"Santa Ana, CA, USA","city":"Santa Ana","stateProvince":"CA"},"frontendLink":"/job-posting/planet-13/quality-control-specialist/2bfc654ecbc92561d6023c92849c043c","title":"Quality Control Specialist","hash":"2bfc654ecbc92561d6023c92849c043c","postingUrl":"https://mmdevelopmentcompanyinc.applytojob.com/apply/nQuV6M25i8/Quality-Control-Specialist"},{"employmentType":"Full-time","postedOn":"8 days ago","description":"<div><p>QUALITY CONTROL TECHNICIAN Whistler Medical Marijuana Corporation is a wholly owned subsidiary of Aurora Cannabis Enterprises Inc. We are currently recruiting for a Quality Control Technician to join our Facility in Pemberton, British Colombia. The incumbent will report to the Vice President of Quality and will be responsible for the following: MAIN RESPONSIBILITIES: Understand, and follow all department SOPs and related forms to GMP and/or GPP standards, including owning QC procedures. Understanding of Health Canada, USP, EU compliance and requirements. Complete all required documentation using good documentation practices, Develop and align testing specifications for all controlled materials and finished products within Aurora Cannabis standards Maintain functional understanding of HPLC, GC-MS, ICP-MS, spectroscopy, and plant sciences Be responsible for the execution of Quality Control process, including but not limited to: Material Management – sampling, testing, and approval of certificate of analysis of controlled materials. Provide guidance to procurement for suitability of material and vendors Environmental Monitoring – participate in the development and execution of the sampling plan of grow rooms, report state of facility and procedures to minimize risk of contamination Compile specification documents for all tested materials, determine the disposition of the material by assessing compliance of the results to the specification Initiate/Support investigations, to ensure ongoing compliance, to achieve process / quality improvements Be the primary contact and liaison for all communication with outside testing labs Be responsible for sampling and testing of cannabis products both internally and externally to ensure compliance with internal specifications and other needs Consult and/or participate in any sampling process required at the site, with respect to suitability, and compliance Reporting of any potential or actual deviations to Process manager and QA Manager Effective and strong communication with all cross functional teams within the facility Support Quality Assurance as required at the facility Attend and participate in meetings as required Any other suitable duties as assigned by the VP of Quality. DESIRED QUALIFICATIONS: B.Sc. degree or diploma in an applicable discipline of science (chemistry, biochemistry, biology or related) 2+ years experience working in Quality Assurance Knowledge of GMP and regulations for manufacturing and testing pharmaceutical products considered an asset Familiarity with laboratory equipment (e.g. HPLC, GC, and ICP) considered an asset. Proficiency in scientific writing Strong verbal and written communication skills. Strong computer skills. Knowledge with Microsoft excel, word and outlook Ability to thrive in a constantly changing environment. We would like to thank all applicants for their interest but only those selected for an interview will be contacted</p></div>","company":{"website":"cannimed.ca","companyType":"Public/Established","name":"Cannimed By Aurora","logoUrl":"/logos/cannimed-bf99b9c93458faff6d96dc9f331679ce.png"},"location":{"country":"Canada","address":"Corman Park No. 344, SK (+1 other)","city":"Corman Park No. 344","stateProvince":"SK"},"frontendLink":"/job-posting/cannimed-by-aurora/quality-control-technician/96c455f4a306fbceecbccecca2231247","title":"Quality Control Technician","hash":"96c455f4a306fbceecbccecca2231247","postingUrl":"https://ca.trabajo.org/job-51-20210509-e05dbc22671c433de8e2db482e4b29c4"},{"postedOn":"11 days ago","description":"<div>Our client, industry leading Cannabis Testing Laboratory based in Arizona, is searching for a Quality Control Manager with previous Cannabis Industry experience to join their growing team.<br /><br />In this role, the successful applicant will be responsible for overseeing the operation of the Cannabis Testing Laboratory department, and the efficacy of the overall program to ensure the utmost in customer satisfaction.<br /><br />The Quality Control Manager will also be responsible for ensuring continual quality improvement within the facility. If you have a strong background in quality management and exceptional leadership abilities, we encourage you to apply.<br /><br />** In order to be considered for this position, previous Cannabis Testing Laboratory experience is required.<br /><br /><b>Job Duties and Responsibilities:</b><br /><ul><li>Establish QMS policy, procedures and report to management on the performance.</li><li>Responsible for accuracy and timely inspections on all instruments in the testing laboratory.</li><li>Lead a team of Quality Engineers, Inspectors, Auditors, Analyst and Technicians.</li><li>Work closely with customers, employees, contractors and outsourcing firms to develop product requirements.</li><li>Successful completion of proficiency testing samples and initial demonstration of capability to demonstrate competence as required for certifications or customer requests.</li><li>Ensure existing procedures and the drafting of new procedures under the supervision of the Laboratory Manager.</li></ul><b>Preferred Skills and Requirements:</b><br /><ul><li>Bachelor's degree in related field</li><li>2+ years of quality management experience</li><li>2-3+ years of analytical laboratory experience</li><li>Proficiency with laboratory testing instruments</li><li>Impeccable communication, presentation and organizational skills</li><li>Experience with Quality Management Systems and data review</li><li>Proficient in computer technology and Microsoft Office</li><li>Ability to work in a team environment</li><li>ISO 17025 experience</li><li>Excellent analytical and problem solving skills</li></ul><b>Salary:</b> $75,000 - $80,000 Plus Benefits<br /><br />If this sounds like the cannabis industry position you have been waiting for, please apply using the online application or the link below - all inquiries are strictly confidential. Our focus is to assist you to make your best next career move, and we will not use your information for any other purpose.<br /><br />CannabizTeam is an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status. TEAM200<br /><br />www.CannabizTeam.com</div>","company":{"companyType":"Private/Growth","name":"CannabizTeam","logoUrl":"/logos/cannabizteam-71e68432a5b2ab7a22442dc51667849a.jpeg"},"location":{"country":"United States","address":"Flagstaff, AZ 86001","city":"Flagstaff","stateProvince":"AZ"},"frontendLink":"/job-posting/cannabizteam/quality-control-manager/302631ca107332d4b661495fccf09a22","title":"Quality Control Manager","hash":"302631ca107332d4b661495fccf09a22","postingUrl":"https://www.indeed.com/job/quality-control-manager-7e2104eaabb17270"},{"employmentType":"Full-time","postedOn":"11 days ago","description":"<div><p><b>Summary: </b></p><p>The Quality Assurance Manager (QAP) will be responsible for the coordination of work to ensure the successful implementation of Cannabis Act, Cannabis Regulations, Good Manufacturing Practices (GMP) and Good Production Practices (GPP) production standards in pursuance of regulatory compliance and achievement of business goals. The QAP will work hand in hand with production, maintenance, facilities and shipping teams to ensure that quality standards are recognized, implemented, enhanced and maintained throughout all of production operations.</p><p><b>Key Responsibilities: </b></p><ul><li>Provides oversight on the performance of all Quality Assurance (QA) personnel, practices, and procedures</li><li>Serves as the Health Canada Compliance Manager and one of the primary contracts for Health Canada</li><li>Initiates the development and ongoing amendment of the organization’s Standard Operating Procedures (SOPS)</li><li>Serves as the internal compliance auditor ensuring the organization’s compliance with all regulatory rules and regulations</li><li>Ensures that the QA practices at each of the organization’s facilities align with the company’s business plan and GMP/GPP standards</li><li>Develops and executes product quality and yield improvement strategies</li><li>Assures regulatory requirements are embodied in all of the organization’s policies, directives, practices, processes and forms</li><li>Establishes and maintains product quality documentation by writing and updating quality assurance procedures</li><li>Establishes the following quality and reliability standards by studying their respective requirements, processes, and procedures:</li></ul><p>· Raw material standards<br />o In-process product inspection standards<br />o Standards for the disposition of finished products<br />o Rework standards</p><ul><li>Maintains and improves product quality by enforcing QA policies and procedures and government requirements; completing product, company, system, and compliance audits; investigating customer complaints; and collaborating with members of senior management to develop new product and engineering designs as well as manufacturing and training methods</li><li>Develops QA plans by conducting hazard analyses; identifying critical control points and preventative measures; establishing critical limits, monitoring procedures, corrective actions and verification procedures</li><li>Prepares product and process quality reports by collecting, analyzing and summarizing information and trends</li><li>Assists in regulatory submission activities from the development/investigational stage through to filing, approval, and post market submissions</li><li>Develops regulatory strategies for current and future programs in collaboration with other senior management</li><li>Provides expertise and support to regulatory inspections including quality representation on all activities</li><li>Develops, updates, and maintains quality systems and manuals that comply with the Cannabis Regulations, Cannabis Act, and GMP/GPP standards</li><li>Investigates product non-conformances; reviews material, document findings and responses for complaints. Manages product holds, reprocessing actions, and final disposition processes for non-compliant resources</li><li>Enforces regulatory requirements in addition to reading and being familiar with the organization’s security directives</li><li>Directs activities of the Quality Assurance department which support the company’s quality vision</li><li>Maintains QA staff by working the Human Resources Manager to recruit, select, orientate, and train of the department employees</li><li>Participates in developing quality metrics and goals, leading efforts in rolling them out to the organization’s facilities</li><li>Provides guidance on production processes where applicable, including troubleshooting, GMP/GPP compliance, and control of contaminants</li><li>Communicates with Operations and Production Technology Manager and relevant facility staff including Master Growers and Quality Assurance personnel</li><li>Ensure investigation and annual product review are conducted in a compliant matter</li></ul><p><b>Qualifications: </b></p><ul><li>BSc/MSc in Chemistry/Biochemistry/Biology/Food or similar discipline. MSc is preferred.</li><li>3-5 years of experience in a QA/Regulatory manufacturing environment.</li><li>Existing CTLS security clearance for QAP.</li><li>Experience in managing Quality Management Systems and creating Preventative Control Plans</li><li>Strong understanding of Health Canada, and GMP/GPP requirements for pharmaceutical, health, food processing, and cannabis products.</li></ul><p>Job Type: Full-time</p><p>Schedule:</p><ul><li>8 hour shift</li></ul><p>Work remotely:</p><ul><li>No</li></ul></div>","company":{"companyType":"Private/Growth","name":"Choice Growers","logoUrl":"/logos/choice-cannabis-727bb8f333cd8f62c23ce3298e046e32.png"},"location":{"country":"Canada","address":"Strathmore, AB","city":"Strathmore","stateProvince":"AB"},"frontendLink":"/job-posting/choice-growers/quality-assurance-manager/2babcd7c97515f768ca5295ba1f9d249","title":"Quality Assurance Manager","hash":"2babcd7c97515f768ca5295ba1f9d249","postingUrl":"https://ca.indeed.com/job/quality-assurance-manager-f721201e3b282c07"},{"employmentType":"Full-time, Permanent","postedOn":"9 days ago","description":"<div><div><div><b>Quality Assurance Associate</b></div><div><b>Introduction</b></div><div>We are looking for a full-time Junior QA Associate to add to our growing cannabis manufacturing company located in St Thomas Ontario. The junior QA will be responsible for managing documentation, coordinating activities with production teams, keeping track of production inventory.</div><div>The incumbent will report to the VP of Quality Assurance and Regulatory Affairs and will be responsible for supporting the quality operations including training, auditing, document control, record keeping, and ensuring compliance with all applicable regulations.</div><div><b>Main Responsibilities</b></div><div></div><ul><li><br />Ensure that all staff are following the approved SOPs, Good Production Practices (GPP), Good Documentation Practices (GDP).</li><li>Ensure production teams are following the established procedures and policies for production of cannabis products.</li><li>Assist in drafting and implementing new SOPs to ensure continuous compliance.</li><li>Keeping track of production and shipping documents to ensure that inventory on hand is up to date.</li><li>Review production batch records (PBRs) for accuracy and completeness.</li><li>Assist QA lead in investigating complaints, completion of deviation and CAPA reports.</li><li>Coordinate with shipping and receiving in charge for tracking the cannabis, raw material, and production supplies.</li><li>Perform daily inspections of production areas including sanitation checks, scales calibration, packaging monitoring, product labels control etc.</li><li>Other jobs as assigned.</li></ul><div><b>Skills</b></div><ul><li>Previous work experience in a Cannabis, food, agriculture, research, or pharmaceutical industry.</li><li>Strong computer skills.</li><li>Excellent written and verbal communication skills.</li><li>Ability to multitask, strong attention to detail, and a positive attitude.</li><li>Experience working in a fast pace environment and adapt to an evolving environment.</li><li>Understanding of Cannabis regulations, GPP, and GDP.</li></ul><div><b>Job Types: Full-time, Permanent</b></div><div></div><ul><li><br />8 hour shift</li></ul><div><b>Education and Experience:</b></div><div></div><ul><li><br />Bachelor's Degree or equivalent qualification.</li><li>Security clearance from Health Canada (preferred).</li><li>Quality Assurance experience at least 1 year.</li></ul></div><div></div></div>","company":{"companyType":"Private/Growth","name":"Sensi Brands","logoUrl":"/logos/sensi-brands-cbc7e6f22068c92c3ba099be4f852aea.png"},"location":{"country":"Canada","address":"St. Thomas, ON","city":"St. Thomas","stateProvince":"ON"},"frontendLink":"/job-posting/sensi-brands/quality-assurance-associate/802c44df4e4c363ff2dbb68bd177ac69","title":"Quality Assurance Associate","hash":"802c44df4e4c363ff2dbb68bd177ac69","postingUrl":"https://ca.indeed.com/job/quality-assurance-associate-e859edeaba36820f"},{"employmentType":"Full-time, Permanent","postedOn":"10 days ago","description":"<div><p><i>Quality Control Technician</i><br />We are looking for a well-organized, detail-oriented individual to join our quality team. This individual will work in collaboration with all of the departments to promote a culture of continuous improvement.</p><p>Responsibilities:</p><ul><li>Perform in-process control monitoring such as swabbing equipment and rooms for micro contamination, water testing, air quality testing, environmental control verification, equipment calibration, pest control</li><li>Track and analyse all test results to determine process effectiveness and optimization</li><li>Inspection of in process and finished product</li><li>Preparation of lot release reports</li><li>Preparation of cannabis samples to be transferred to approved 3rd party testing laboratories</li><li>Identify non-conformities, determine appropriate corrective and preventive action</li><li>Assist with all laboratory tasks, laboratory equipment management, method validations, microbiology, cannabinoid potency, moisture analysis, foreign material inspection</li><li>Assist in authoring and updating Standard Operating Procedures to support Good Manufacturing Practices</li><li>Ensure all documentation and processes are approved by the Quality Assurance Person</li><li>Assist with quality investigations when required</li><li>Maintain understanding of all procedures and applicable regulations</li><li>Support Health Canada Inspections</li><li>Assist in preparation and management of future Extraction Division</li><li>Other duties as assigned</li></ul><p>Education:</p><ul><li>Minimum College diploma/ Bachelor’s degree or equivalent in related scientific field with regulatory discipline required</li><li>1-2 years of education and/or experience in microbiology/chemistry preferred</li></ul><p>Other:</p><ul><li>Understanding of sampling protocols, sampling plans, test methodology, test method limitation, validation, and risk assessment analysis an asset</li><li>QC experience in a GMP-focused quality related position or experience in cannabis industry environment is an asset</li><li>This is a full time position</li><li>Will be required to complete security clearance/ police check</li></ul><p>Job Types: Full-time, Permanent</p><p>Salary: $18.00-$22.00 per hour</p><p>Benefits:</p><ul><li>Casual dress</li><li>Dental care</li><li>Extended health care</li><li>Life insurance</li><li>On-site parking</li><li>Vision care</li></ul><p>Schedule:</p><ul><li>8 hour shift</li><li>Day shift</li><li>Holidays</li><li>Monday to Friday</li><li>Overtime</li></ul><p>COVID-19 considerations:<br />Daily screening and temperature check upon entering facility. Mask, Face Shield, scrubs and gloves required. Social distancing and cohorts in place. Frequent cleaning and sanitizing of common areas.</p><p>Work remotely:</p><ul><li>No</li></ul></div>","company":{"companyType":"Private/Growth","name":"Muskoka Grown","logoUrl":"/logos/muskoka-grown-7cb5a54b423f6197f4ba70709ad76a65.jpeg"},"location":{"country":"Canada","address":"Bracebridge, ON","city":"Bracebridge","stateProvince":"ON"},"frontendLink":"/job-posting/muskoka-grown/quality-control-technician/873b74f0e9bb06d4809f6399af10f762","title":"Quality Control Technician","hash":"873b74f0e9bb06d4809f6399af10f762","postingUrl":"https://ca.indeed.com/job/quality-control-technician-84c19335448c1e3c"},{"employmentType":"Full-time, Permanent","postedOn":"10 days ago","description":"<div><p><b>About AtlantiCann Medical</b></p><p>AtlantiCann Medical is majority owned by the Mi’kmaq First Nations of Nova Scotia.</p><p>We are proud to be producing quality cannabis in Mi’kma’ki, the ancestral and unceded territory of the Mi’kmaq People. The 8-point star, a symbol very important to the Mi’kmaq community, often presents with 4 colours signifying unity between the four races of people as well as the 4 directions (North, South, East and West), emphasizing balance within oneself and mother earth.</p><p>We are proud to embrace these values and provide Mi’Kmaq product to NS and across the nation.</p><p>We are an equal opportunity employer and adhere to fair employment practices.</p><p>As a Quality Assurance (QA) Technician of a Health Canada Licensed Producer of Cannabis, you will be responsible for quality monitoring, documentation, records handling, and quality control in compliance with Health Canada’s Cannabis Regulations and the European Union GMP Regulations, while taking corrective and preventative measures if necessary.</p><p><b>Roles Responsibilities</b></p><ul><li>Staying current with Health Canada regulations.</li><li>Staying current with European GMP Regulations</li><li>Keeping all records up to date and compliant to regulatory standards in preparation for Health Canada, and EU-GMP audits.</li><li>Working with the Quality Assurance Technician to ensure proper documentation.</li><li>Inventory reporting to Health Canada and Canada Revenue Agency.</li><li>Ensuring all processing activities are completed as per Standard Operating Procedures (SOPs).</li><li>Understanding, implementing, and training on Good Production Practices (GPP).</li><li>In-process quality monitoring and testing.</li><li>Draft, revise, and review SOPs.</li><li>Train staff on SOPs and ensure ongoing compliance.</li><li>Review batch records and lab certificate of analysis and ensuring that all cannabis is approved prior to being made available for sale.</li><li>Sanitation program inspection and verification.</li><li>Record keeping and documentation.</li><li>Responsible for investigating every complaint received in respect of the quality of the cannabis and taking any measures to mitigate risk.</li><li>Development and maintenance of a recall program</li><li>Responsible for approving the preventive control plan for activities conducted with cannabis extract or edible cannabis</li><li>Responsible for approval of methods and procedures related to GPP</li><li>Preparing representative batch samples for lab testing and retention.</li><li>Configuring and monitoring seed-to-sale software (Ample Organics).</li><li>Reporting to senior management.</li><li>Identify and investigate deviations and perform corrective and preventative actions.</li></ul><p><b>Required Qualification</b></p><p><b>Formal Education or Equivalent: </b></p><ul><li>Science degree or equivalent</li><li>Quality Assurance Certificate an asset</li><li>The technical knowledge, experience, and training to fulfill the responsibilities as required by Health Canada Cannabis Regulations</li><li>Previous quality assurance experience in cannabis, pharmaceuticals, medical or food production required.</li><li>HACCP training/certificate is an asset.</li></ul><p><b>Years of Experience: </b></p><ul><li>2-5 years in a quality assurance role at a licensed cannabis producer is an asset.</li></ul><p><b>Competencies, Specialized Skills or Knowledge unique to this role: </b></p><ul><li>Previous quality assurance experience in cannabis is an asset.</li><li>Security Clearance will be required for this position. Previous security cleared status is an asset.</li><li>Must be qualified to be the Alternate Quality Assurance Person under Health Canada requirements.</li></ul><p><b>Performance Metrics</b> ·</p><ul><li><i>Professionalism</i>: Meeting compliance with regulations at all times</li><li><i>Communication: </i>Lead HC inspections with efficiency and politeness.</li><li><i>Accountability: </i>Identifying and taking preventive measures in response.</li><li><i>Learning &amp; Development: </i>Training new hires on SOP’s and re-training expectations.</li><li><i>Flexibility: </i>Keeping up to date with HC regulations and ensuring SOP meet the requirements.</li><li><i>Efficiency: </i>Reviewing and executing records upon completion.</li><li><i>Leadership: </i>Coaching staff on Health Canada Compliance.</li></ul><p><b>Physical requirements</b></p><ul><li>The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.</li><li>Ability to lift, push, and pull 50 pounds</li><li>Ability to sit, squat, bend, and kneel repetitively throughout an 8 or 10-hour day</li><li>Ability to stand and walk for extended periods of time</li><li>Ability to visually identify plant health issues, safety hazards, and signage</li><li>§ Ability to use a ladder up to 12-20 feet high</li></ul><p><b>Expected Hours of Work; </b>This is a full-time position that requires but is not limited to, 40 hours per week. Operational hours are dependent on the client and facility operations. This position may be required to work weekends and holidays.</p><p>The Quality Assurance Technician will report to the Quality Assurance Manager.</p><p>Have reliable transportation to and from the facility.</p><p><b>Environmental Conditions</b></p><ul><li>The QA Technician may be exposed to pollen, allergens, and chemical pesticides at the facility. As well as fumes, dust, odors, extreme heat temperatures, heights, indoor AC, no AC, motion, noise, protective gear, vibrations, and water.</li></ul><p>Job Types: Full-time, Permanent</p><p>Benefits:</p><ul><li>Casual dress</li><li>Dental care</li><li>Employee assistance program</li><li>Extended health care</li><li>Life insurance</li><li>On-site parking</li><li>Vision care</li></ul><p>Schedule:</p><ul><li>10 hour shift</li><li>8 hour shift</li><li>Day shift</li><li>Holidays</li><li>Monday to Friday</li><li>On call</li><li>Overtime</li><li>Weekends</li></ul><p>Work remotely:</p><ul><li>No</li></ul></div>","company":{"name":"AtlantiCann Medical Inc"},"location":{"country":"Canada","address":"Lower Sackville, NS","city":"Lower Sackville","stateProvince":"NS"},"frontendLink":"/job-posting/atlanticann-medical-inc/quality-assurance-technician/63fe4096fbcf58245c4054870e794769","title":"Quality Assurance Technician","hash":"63fe4096fbcf58245c4054870e794769","postingUrl":"https://ca.indeed.com/job/quality-assurance-technician-8e5fa67d73c976b9"},{"employmentType":"Full-time","postedOn":"11 days ago","description":"<div><p>Quality Control Technicians are responsible for the efficiency and quality of cannabis by trimming, manicuring and preparing product for sale. We are currently seeking motivated, dependable people to fill entry level positions into the medical cannabis industry. Must have reliable transportation. Must be able to stand for long periods of time. Hiring Immediately. No experience required.</p><p>Duties and Responsibilities:</p><p>-Responsible for trimming (minimum of 1/2 pound per hour) and manicuring cannabis in a timely, efficient manner to prepare product for sale.</p><p>-Working respectfully and collectively with other Quality Control team members</p><p>-Follow all safety regulations set by team leaders</p><p>-Ensure consistent quality</p><p>-Ensure an overall positive, safe and clean environment</p><p>Qualifications:</p><p>-Must be able to pass state and federal background checks</p><p>-Experience and knowledge in manufacturing / laborer industry preferred but not required</p><p>-Ability to work in a fast paced environment</p><p>-Ability to handle high stress situations</p><p>-Self Motivated</p><p>-Ability to multi-task</p><p>-Must be at least 21 years of age and authorized to work in the US.</p><p>-Must be willing to work 7 days a week if necessary, and to be flexible with schedule.</p><p>-Ability to work 4 10 hour shifts</p><p>-Exposure to fertilizer, dusts, odors, allergens, pollen, and other environmental variables.</p><p>Education:</p><p>-Minimum High School or G.E.D. equivalent required</p><p>Benefits:</p><ul><li>Private medical/dental insurance</li><li>Life insurance</li></ul><p>Job Type: Full-time</p><p>Pay: $14.00 - $16.00 per hour</p><p>COVID-19 considerations:<br />Follows all COVID-19 protocol.</p><p>Edit job<br />Status: Open<br />View public job page</p><p>Details<br />Created: January 5, 2021<br />Views: 1,547<br />Curated Candidates: 180 total<br />Add a candidate<br />Find candidates</p><p>Budget<br />Job Budget: Not sponsored<br />Sponsor job</p><p>Job Type: Full-time</p><p>Pay: $14.00 - $16.00 per hour</p><p>Benefits:</p><ul><li>Dental insurance</li><li>Health insurance</li><li>Paid time off</li><li>Vision insurance</li></ul><p>Schedule:</p><ul><li>8 hour shift</li></ul><p>COVID-19 considerations:<br />We adhere to all COVID-19 protocols and precautions.</p><p>Application Question(s):</p><ul><li>Are you at least 21 years of age and authorized to work in the US?</li></ul><p>Education:</p><ul><li>High school or equivalent (Preferred)</li></ul><p>Experience:</p><ul><li>Manufacturing: 1 year (Preferred)</li></ul><p>Work Location:</p><ul><li>One location</li></ul><p>Work Remotely:</p><ul><li>No</li></ul></div>","company":{"companyType":"Private/Established","name":"NSMC"},"location":{"country":"United States","address":"White Hall, AR 71602","city":"White Hall","stateProvince":"AR"},"frontendLink":"/job-posting/nsmc/quality-control-technician/1ffe5ac72987e4252f45082685422b80","title":"Quality Control Technician","hash":"1ffe5ac72987e4252f45082685422b80","postingUrl":"https://www.indeed.com/job/quality-control-technician-95ac25f681fe3af9"},{"employmentType":"Full-time, Permanent","postedOn":"11 days ago","description":"<div><p><i>Quality Assurance/Control Supervisor </i><br />Under the direction of the Quality Assurance Manager, the Quality Assurance/Control Supervisor is primarily responsible for the monitoring and quality control of cannabis production and processing within the facility. The role will also be responsible for ensuring compliance with the Cannabis Act and Good Production Practices (GPP). The Quality Assurance/Control Supervisor will be able to communicate with management and production team effectively. They will be energetic and a team player by excellence.</p><p><b>Job Duties: </b></p><ul><li>Ensure that Quality Assurance and Production Standard Operating Procedures are strictly followed and enforced.</li><li>Continuous SOP revisions, creation of new Standard Operating Procedure’s and protocols through the internal Quality Management Software.</li><li>Supporting in implementation and training of current SOP’s.</li><li>Update, develop and implement logs for Quality Assurance Operations.</li><li>Ensure compliance with Cannabis Act and Cannabis Regulations.</li><li>Familiar with Cannabis Regulations, Controlled Substances Act. Pest Control Act, Food and Drug Act and Ontario Health and Safety Act.</li><li>Collaborate with other departments to ensure compliance with standard operating procedures.</li><li>Implement GPP within the production environment, develop and implement quality documents.</li><li>Perform in-process QA inspections and ensure that all activities within production area are executed as per defined SOPs.</li><li>Conduct QC internal tests as ATP Swabs Testing, Moisture Content of in process/final product and create reports in compliance with companies’ policies, practices, and procedures.</li><li>Conduct inspection and approval of in-coming materials for production and ensure they are by approved by Quality before usage.</li><li>Perform product sampling and coordinate product testing with the approved testing lab.</li><li>Assist in development of Corrective and Preventative Actions as per production process.</li><li>Perform any other tasks assigned by the management.</li><li>Familiar with Quality Management Software-Microsoft Enterprise Cloud.</li><li>Develop an internal calibration program of equipment in Good Production Practices areas and maintain external calibration data and documentation.</li><li>Develop and assist in internal auditing/inspection program.</li></ul><p><b>Requirements: </b></p><ul><li>1-5 years of work experience in a quality assurance role in pharmaceutical, food, cosmetics or related industry.</li><li>Post-secondary degree or diploma in biological science (chemistry, plant biology, pharmacology).</li><li>1+ years working in the cannabis industry.</li><li>Cannabis Act and other cannabis regulations knowledge is an asset.</li><li>Experience with an organization regulated by Health Canada or experience in a similarly regulated environment (GPP, GMP, GAP).</li><li>Ability to follow strict operating procedures.</li><li>Ability to work individually as well as part of a team.</li><li>Ability to adapt to new technologies.</li><li>Dedication to safety measures and best practices.</li><li>Ability to prioritize and manage conflicting demands.</li><li><b>Must have, or be able to obtain a HEALTH CANADA Security Clearance. Those with current security clearance will be given priority for the role.</b></li></ul><p><b>Job Conditions: </b></p><ul><li>Will be in contact with Cannabis and its components/derivatives.</li><li>Use of required personal protective equipment.</li></ul><p>Job Types: Full-time, Permanent</p><p>Salary: $40,000.00-$60,000.00 per year</p><p>Benefits:</p><ul><li>Casual dress</li><li>Dental care</li><li>Disability insurance</li><li>Extended health care</li><li>Life insurance</li><li>On-site parking</li><li>Vision care</li></ul><p>Schedule:</p><ul><li>8 hour shift</li><li>Day shift</li><li>Monday to Friday</li><li>On call</li><li>Weekends</li></ul><p>Education:</p><ul><li>Bachelor's Degree (required)</li></ul><p>Experience:</p><ul><li>Quality Assurance: 1 year (required)</li></ul><p>Work remotely:</p><ul><li>No</li></ul></div>","company":{"companyType":"Private","name":"THPC"},"location":{"country":"Canada","address":"Brantford, ON","city":"Brantford","stateProvince":"ON"},"frontendLink":"/job-posting/thpc/quality-control-supervisor/55291565431a8013b419f17c21067a3f","title":"Quality Control Supervisor","hash":"55291565431a8013b419f17c21067a3f","postingUrl":"https://ca.indeed.com/job/quality-control-supervisor-4b07a7f3d3811245"},{"employmentType":"Full-time","postedOn":"11 days ago","description":"<div><p>Reporting to the CEO and other senior-level management, the Quality Assurance Person (QAP) is the Quality Assurance Manager within the licensed site. The QAP is responsible for the verification and validation of quality assurance, ensuring that cannabis products produced meet the organization’s objectives for quality, safety, regulatory, and customer expectations in accordance with the Cannabis Act and relevant regulations.</p><p>The QAP will advise on, establish and monitor quality management systems and coordinate activities to meet production process and product quality standards for the outdoor cultivation and processing facility.</p><p>This role will require being onsite in Whitehorse, Seasonally (May-November) with year-round QAP responsibility. Relocation will be supported for this position.</p><p><b>Responsibilities:</b></p><p>• Manage the licensed site’s Quality Assurance Department and lead in developing, reviewing, and maintaining SOPs &amp; quality management programs and projects to ensure compliance under the Cannabis Act/Regulations. Work cross-departmentally to implement SOPs (i.e. operations, regulatory, security).</p><p>• Develop training programs around SOPs pertaining to GPP and record-keeping compliance.</p><p>• Create quality control programs/systems for cannabis storage.</p><p>• Develop programs around GPP &amp; record-keeping methods for sanitation of premises, equipment, cleanliness, hygienic behavior of personnel, and facility maintenance.</p><p>• Establish and maintain record-keeping systems and ensure employee adherence to proper documentation practices.</p><p>• Conduct testing on each lot or batch of cannabis prior to release for sale; ensure testing is conducted using validated methods, investigating deviations and out-of-spec results.</p><p>• Develop and perform internal audits regularly to determine quality assurance compliance according to Cannabis Regulations.</p><p>• Perform analysis of reports and production data to identify trends and recommend updates or changes to quality standards and procedures when necessary.</p><p>• Maintain current knowledge of best practices for the provisions of the Cannabis Act and Cannabis Regulations that apply to the license holder.</p><p><b>Required Responsibilities as per Cannabis Regulations:</b></p><p>• Function as QAP to support in all matters relating to Good Production Practices (GPP) and record-keeping compliance during Health Canada inspections.</p><p>• Review and approve methods and procedures pertaining to Cannabis Regulations within the licensed site.</p><p>• Investigate complaints regarding the quality of cannabis production and ensure immediate corrective action when necessary; take corrective and preventative measures.</p><p>• Ensure cannabis quality meets standards prior to release for sale.</p><p>• Submit, secure and maintain a valid security clearance.</p><p><b>Qualifications:</b></p><p>• Degree in Chemistry, Biology, Pharmacology or Food Science, obtained or recognized by a Canadian university.</p><p>• 5+ years’ senior management experience in Quality Assurance/Control in a production environment.</p><p>• Valid HC security clearance (or ability to obtain one).</p><p>• Solid ERP, eQMS, CTLS reporting experience.</p><p>• Proven knowledge and experience in the stated responsibilities of the position (i.e. Food, Pharma, NHP).</p><p>• Previous experience as a stand-alone QA/QC resource having direct responsibility for determining strategic objectives to meet quality with given resources and carry out tactical execution.</p><p>• Preferred experience with cGMP, GAP, GLP, HACCP, ISO, and FDA</p></div>","company":{"companyType":"Private/Startup","name":"Cannabis At Work","logoUrl":"/logos/cannabis-at-work-8ae63b190226a7031617f4393f916a20.jpeg"},"location":{"country":"Canada","address":"Whitehorse, YT","city":"Whitehorse","stateProvince":"YT"},"frontendLink":"/job-posting/cannabis-at-work/quality-assurance-person/e9aa83314b15b327959f16e08d2a8c07","title":"Quality Assurance Person","hash":"e9aa83314b15b327959f16e08d2a8c07","postingUrl":"https://ca.linkedin.com/jobs/view/quality-assurance-person-at-cannabis-at-work-2519093629"},{"postedOn":"12 days ago","description":"<div><div><p><b>About </b><b>Charlotte's Web:</b></p><p>Charlotte's Web products are made from our world-renowned hemp genetics grown 100% in the USA.<br />Founded by the Stanley Brothers of Colorado, Charlottes Web leads the industry in quality, safety, consistency and social responsibility to improve thousands of lives daily through the use of Charlotte's Web.<br />At Charlottes Web, we are driven by principles that extend far beyond the bottom line. It is our goal to provide products of the highest possible quality, while contributing to the sustainability of the communities we have the privilege of serving.</p><p></p><p><b>Position Summary:</b></p><p>The primary responsibility of this position is to execute against the procedures for the manufacture, storage, and distribution of dietary supplements. This position requires utilization of the Code of Federal Regulations (21 CFR Part 111), including but not limited to control of raw materials, components, intermediates and final products.</p><p><b><br />Essential Duties and Responsibilities:</b></p><ul><li>Own and perform raw material quality disposition</li><li>Provide a broad range of quality oversight for the warehouse and raw materials program</li><li>Perform compliance review on the following records: batch record (includes on-the-floor review of records); release data</li><li>Determine raw material disposition</li><li>Initiate and own Deviations, CAPAs, and change controls as appropriate</li><li>Work directly with manufacturing, the laboratory and other departments responsible for GMP activities to resolve deviations and other compliance issues in a timely manner</li><li>Perform warehouse walk-through on a regular basis to maintain area in cGMP compliance state</li><li>Support internal audits of departments involved in GMP activities</li><li>Assist in other Quality Assurance activities as needed, i.e. Batch Record Review, Equipment Log Review</li><li>Support client and regulatory audits</li><li>React to change productivity and handle other essential tasks</li></ul><p></p><p><b>Qualifications:</b></p><ul><li>Bachelors Degree in Engineering (Biomedical, Mechanical, Chemical, or Electrical) or Science (Biology) preferred</li><li>1-2 years experience in a Quality Assurance role for medical device, food, dietary supplement or pharmaceutical manufacturing</li><li>Experience handling Co-Manufacturer compliance required</li><li>Demonstrates excellent organizational and communication skills and proficiency with the MS Office Suite, and statistical software</li><li>Must be able to work independently with minimal supervision</li><li>Able to prioritize projects and manage Quality Assurance resources to meet organizational goals and objectives</li></ul><p></p><p><b>Compensation:</b></p><p>$18.55 - $27.85</p><p></p><p>Charlottes Web provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.</p><p>This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training. Charlottes Web is an At-Will Employer.</p><p>V1.0</p></div></div>","company":{"companyType":"Public/Established","name":"Charlottes Web","logoUrl":"/logos/charlottes-web-hemp-902e2edc0fd77f5d49ab925ac37fc7b6.png"},"location":{"country":"United States","address":"Louisville, CO 80027","city":"Louisville","stateProvince":"CO"},"frontendLink":"/job-posting/charlottes-web/quality-assurance-associate/361470cf76b212ade7d2f47330d60c19","title":"Quality Assurance Associate","hash":"361470cf76b212ade7d2f47330d60c19","postingUrl":"https://www.indeed.com/job/quality-assurance-associate-2f351a5cd3d1a645"}]