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Quality Manager

Cresco Labs Indiantown, FL, USA Full-time
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COMPANY OVERVIEW

Recently named one of Entrepreneur magazine’s Top 100 Cannabis Leaders, Cresco Labs is one of the largest vertically-integrated multi-state cannabis operators in the United States. Cresco is built to become the most important company in the cannabis industry by combining the most strategic geographic footprint with one of the leading distribution platforms in North America. Employing a consumer-packaged goods (“CPG”) approach to cannabis, Cresco’s house of brands is designed to meet the needs of all consumer segments and includes some of the most recognized and trusted national brands including Cresco, Remedi and Mindy’s, a line of edibles created by James Beard Award-winning chef Mindy Segal. Sunnyside*, Cresco’s national dispensary brand is a wellness-focused retailer designed to build trust, education and convenience for both existing and new cannabis consumers. Recognizing that the cannabis industry is poised to become one of the leading job creators in the country, Cresco has launched the industry’s first national comprehensive Social Equity and Educational Development (SEED) initiative designed to ensure that all members of society have the skills, knowledge and opportunity to work in and own businesses in the cannabis industry.

MISSION STATEMENT

At Cresco, we aim to lead the nation’s cannabis industry with a focus on regulatory compliance, product consistency, and customer satisfaction. Our operations bring legitimacy to the cannabis industry by acting with the highest level of integrity, strictly adhering to regulations, and promoting the clinical efficacy of cannabis. As Cresco grows, we will operate with the same level of professionalism and precision in each new market we move in to.

JOB SUMMARY

Cresco Labs is seeking a Quality Manager to support our cultivation/manufacturing facility in Indiantown, FL. As a Quality Manager, you will be be part of the site management team, setting the tone and an example for quality at the site. You will be responsible for overseeing quality-related activities at the facility associated with sampling and inspection of in-process and finished products, hold and release, customer complaints, product investigations, and Corrective and Prevention Action (CAPA) plans.

The Quality Manager will be responsible for current Good Manufacturing Practices (cGMP’s) at the facility along with GMP self-inspections. This individual must be diverse in quality functions related to manufacturing, cultivation and supply chain. Product families include flower, cannabis oil, vape pens/cartridges, and concentrates, and edibles. 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 Quality Manager is responsible for ensuring the facility remains compliant under state and local laws and with applicable certifications. The candidate will have the ability to interpret and apply compliance requirements for various departments with previous experience monitoring, investigating, and resolving inventory discrepancies. The ideal candidate must possess strong leadership skills and operational knowledge, be able to manage a team and partner closely with operations leadership, possess strong attention to detail and have experience working within a highly regulated industry. The ideal candidate must be a change agent with strong influencing skills.

CORE JOB DUTIES.

• Oversee the quality team, including performance management, schedule coverage plan, prioritization of resources and workload, headcount numbers, talent development, and budget management.

• Serves as point of escalation for all quality issues and concerns at the site, including leading strategy and execution plan with production investigations, material bracketing, CAPA, etc..

• Provides timely and executive level summaries to senior leadership with critical quality issues, including conducting status meetings, preparing PowerPoint presentation summaries, identifying risk, establishing timelines, etc.

• Performs in-process and finished product sampling, inspection and disposition including hold, rework, and destruction.

• Overall accountability for product discontinuation, quarantine, destruction, rework, withdrawal/recall to operations and quality management.

• Collaborates with operational functions to troubleshoot product defects, provides advice with process improvements to eliminate errors and reduce risk.

• Consolidates technical information from cultivation operations and other departments and prepares written investigation and CAPA reports which may be provided to state regulators.

• Manages and responds to critical consumer complaints or upward trends and works with key stakeholders on solutions.

• Reviews batch manufacturing records, logbooks, test results, and ensures good documentation practices are followed.

• Responsible for release of all batches/lots.

• Discusses issues and concerns directly with other managers so any corrections and improvements can be made in a timely manner

• Ensures equipment and product line clearances before production runs

• Develop and maintain Master Sanitation Schedules.

• Track and evaluate all testing failures.

• Assist with QMS document writing and revisions, including routing and/or approval of change request packages.

• Inspects packaged orders to ensure correct content and quantities, as deemed necessary.

• Inspects retain samples as deemed necessary.

• Manage and track stability sampling and testing.

• Monitors compliance to established Good Manufacturing Practices (GMP’s), Good Agricultural Practices (GAP’s) and GFSI (Global Food Safety Initiative) guidance such as BRC, SQF, and FSSC 22000.

• Performs GMP facility inspections.

• Participates in corporate Quality internal audits as assigned.

• Maintains Cannabis Safety and Quality (CSQ) third party certification of the site.

• Facilitates creation of and/or updates to HACCP Plans and maintains compliance to all Critical Control Points (CCP’s)

• Conducts all duties in compliance with safety rules, applicable SOPs, and other applicable guidelines.

• Conduct inspections and audits with state and local regulatory and law enforcement agencies

• Collect, audit, and file required operational logs from all departments to ensure compliance

• Collect and file all signed transfer manifests

• Regulatory research and summarizations

• Prepare monthly cultivation and inventory inspection reports

• Monitor inventory losses and assist in developing processes and procedures to reduce loss in all departments

• Ensure full inventory is completed in all departments and investigate/ resolve any inventory discrepancies

• 5-10% travel to other facilities and states to help with new market launches, training, etc.

REQUIRED EXPERIENCE, EDUCATION AND SKILLS

• Bachelor’s degree (in Food Science, Agriculture, Biology, Microbiology, or Chemistry preferred)

• 5 years’ experience in a Quality and/or Compliance role

• Must be HACCP Certified

• Must be Certified in Internal Auditing

• Must be PCQI Certified

• Prior experience in highly regulated industry: healthcare, medical devices, pharmaceutical, consumer packaged goods (food), cannabis, tobacco, dietary supplements, cosmetics, OTC, or personal Care

• Highly desirable: FDA, HACCP, GFSI (Global Food Safety Initiative) such as BRC, SQF, and FSSC 22000

• Prior experience with product sampling, inspection procedures, customer complaints, product investigations, and CAPA

• Prior experience in regulatory agency inspections/audits and correspondence.

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

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

• Strong written and verbal communication skills, including writing executive summaries and communicating with senior level operations, quality management team, and regulatory agencies

• Must be detail-oriented

• Strong analytical skills, including working knowledge of microbiology, chemistry and technical data

• 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":"21 days ago","description":"<div><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 a Quality Manager to support our cultivation/manufacturing facility in Indiantown, FL. As a Quality Manager, you will be be part of the site management team, setting the tone and an example for quality at the site. You will be responsible for overseeing quality-related activities at the facility associated with sampling and inspection of in-process and finished products, hold and release, customer complaints, product investigations, and Corrective and Prevention Action (CAPA) plans.</p><p>The Quality Manager will be responsible for current Good Manufacturing Practices (cGMP’s) at the facility along with GMP self-inspections. This individual must be diverse in quality functions related to manufacturing, cultivation and supply chain. Product families include flower, cannabis oil, vape pens/cartridges, and concentrates, and edibles. 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 Quality Manager is responsible for ensuring the facility remains compliant under state and local laws and with applicable certifications. The candidate will have the ability to interpret and apply compliance requirements for various departments with previous experience monitoring, investigating, and resolving inventory discrepancies. The ideal candidate must possess strong leadership skills and operational knowledge, be able to manage a team and partner closely with operations leadership, possess strong attention to detail and have experience working within a highly regulated industry. The ideal candidate must be a change agent with strong influencing skills.</p><p>CORE JOB DUTIES.</p><p>• Oversee the quality team, including performance management, schedule coverage plan, prioritization of resources and workload, headcount numbers, talent development, and budget management.</p><p>• Serves as point of escalation for all quality issues and concerns at the site, including leading strategy and execution plan with production investigations, material bracketing, CAPA, etc..</p><p>• Provides timely and executive level summaries to senior leadership with critical quality issues, including conducting status meetings, preparing PowerPoint presentation summaries, identifying risk, establishing timelines, etc.</p><p>• Performs in-process and finished product sampling, inspection and disposition including hold, rework, and destruction.</p><p>• Overall accountability for product discontinuation, quarantine, destruction, rework, withdrawal/recall to operations and quality management.</p><p>• Collaborates with operational functions to troubleshoot product defects, provides advice with process improvements to eliminate errors and reduce risk.</p><p>• Consolidates technical information from cultivation operations and other departments and prepares written investigation and CAPA reports which may be provided to state regulators.</p><p>• Manages and responds to critical consumer complaints or upward trends and works with key stakeholders on solutions.</p><p>• Reviews batch manufacturing records, logbooks, test results, and ensures good documentation practices are followed.</p><p>• Responsible for release of all batches/lots.</p><p>• Discusses issues and concerns directly with other managers so any corrections and improvements can be made in a timely manner</p><p>• Ensures equipment and product line clearances before production runs</p><p>• Develop and maintain Master Sanitation Schedules.</p><p>• Track and evaluate all testing failures.</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 as deemed necessary.</p><p>• Manage and track stability sampling and testing.</p><p>• Monitors compliance to established Good Manufacturing Practices (GMP’s), Good Agricultural Practices (GAP’s) and GFSI (Global Food Safety Initiative) guidance such as BRC, SQF, and FSSC 22000.</p><p>• Performs GMP facility inspections.</p><p>• Participates in corporate Quality internal audits as assigned.</p><p>• Maintains Cannabis Safety and Quality (CSQ) third party certification of the site.</p><p>• Facilitates creation of and/or updates to HACCP Plans and maintains compliance to all Critical Control Points (CCP’s)</p><p>• Conducts all duties in compliance with safety rules, applicable SOPs, and other applicable guidelines.</p><p>• Conduct inspections and audits with state and local regulatory and law enforcement agencies</p><p>• Collect, audit, and file required operational logs from all departments to ensure compliance</p><p>• Collect and file all signed transfer manifests</p><p>• Regulatory research and summarizations</p><p>• Prepare monthly cultivation and inventory inspection reports</p><p>• Monitor inventory losses and assist in developing processes and procedures to reduce loss in all departments</p><p>• Ensure full inventory is completed in all departments and investigate/ resolve any inventory discrepancies</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>• Bachelor’s degree (in Food Science, Agriculture, Biology, Microbiology, or Chemistry preferred)</p><p>• 5 years’ experience in a Quality and/or Compliance role</p><p>• Must be HACCP Certified</p><p>• Must be Certified in Internal Auditing</p><p>• Must be PCQI Certified</p><p>• Prior experience in highly regulated industry: healthcare, medical devices, pharmaceutical, consumer packaged goods (food), cannabis, tobacco, dietary supplements, cosmetics, OTC, or personal Care</p><p>• Highly desirable: FDA, HACCP, GFSI (Global Food Safety Initiative) such as BRC, SQF, and FSSC 22000</p><p>• Prior experience with product sampling, inspection procedures, customer complaints, product investigations, and CAPA</p><p>• Prior experience in regulatory agency inspections/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>• Must be detail-oriented</p><p>• Strong analytical skills, including working knowledge of microbiology, chemistry and technical data</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":"Indiantown, FL, USA","city":"Indiantown","stateProvince":"FL"},"frontendLink":"/job-posting/cresco-labs/quality-manager/640c31777cee1c81509b79c9f8c47057","title":"Quality Manager","hash":"640c31777cee1c81509b79c9f8c47057","postingUrl":"https://www.salary.com/job/cresco-labs/quality-manager/8c11a7b7-4bdb-4049-8120-dd92d177950f"},{"employmentType":"Full-time","postedOn":"22 days ago","description":"<div><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 a Quality Manager to support our cultivation/manufacturing facility in Indiantown, FL. As a Quality Manager, you will be be part of the site management team, setting the tone and an example for quality at the site. You will be responsible for overseeing quality-related activities at the facility associated with sampling and inspection of in-process and finished products, hold and release, customer complaints, product investigations, and Corrective and Prevention Action (CAPA) plans.</p><p>The Quality Manager will be responsible for current Good Manufacturing Practices (cGMP's) at the facility along with GMP self-inspections. This individual must be diverse in quality functions related to manufacturing, cultivation and supply chain. Product families include flower, cannabis oil, vape pens/cartridges, and concentrates, and edibles. 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 Quality Manager is responsible for ensuring the facility remains compliant under state and local laws and with applicable certifications. The candidate will have the ability to interpret and apply compliance requirements for various departments with previous experience monitoring, investigating, and resolving inventory discrepancies. The ideal candidate must possess strong leadership skills and operational knowledge, be able to manage a team and partner closely with operations leadership, possess strong attention to detail and have experience working within a highly regulated industry. The ideal candidate must be a change agent with strong influencing skills.</p><p>CORE JOB DUTIES.</p><p>• Oversee the quality team, including performance management, schedule coverage plan, prioritization of resources and workload, headcount numbers, talent development, and budget management.</p><p>• Serves as point of escalation for all quality issues and concerns at the site, including leading strategy and execution plan with production investigations, material bracketing, CAPA, etc..</p><p>• Provides timely and executive level summaries to senior leadership with critical quality issues, including conducting status meetings, preparing PowerPoint presentation summaries, identifying risk, establishing timelines, etc.</p><p>• Performs in-process and finished product sampling, inspection and disposition including hold, rework, and destruction.</p><p>• Overall accountability for product discontinuation, quarantine, destruction, rework, withdrawal/recall to operations and quality management.</p><p>• Collaborates with operational functions to troubleshoot product defects, provides advice with process improvements to eliminate errors and reduce risk.</p><p>• Consolidates technical information from cultivation operations and other departments and prepares written investigation and CAPA reports which may be provided to state regulators.</p><p>• Manages and responds to critical consumer complaints or upward trends and works with key stakeholders on solutions.</p><p>• Reviews batch manufacturing records, logbooks, test results, and ensures good documentation practices are followed.</p><p>• Responsible for release of all batches/lots.</p><p>• Discusses issues and concerns directly with other managers so any corrections and improvements can be made in a timely manner</p><p>• Ensures equipment and product line clearances before production runs</p><p>• Develop and maintain Master Sanitation Schedules.</p><p>• Track and evaluate all testing failures.</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 as deemed necessary.</p><p>• Manage and track stability sampling and testing.</p><p>• Monitors compliance to established Good Manufacturing Practices (GMP's), Good Agricultural Practices (GAP's) and GFSI (Global Food Safety Initiative) guidance such as BRC, SQF, and FSSC 22000.</p><p>• Performs GMP facility inspections.</p><p>• Participates in corporate Quality internal audits as assigned.</p><p>• Maintains Cannabis Safety and Quality (CSQ) third party certification of the site.</p><p>• Facilitates creation of and/or updates to HACCP Plans and maintains compliance to all Critical Control Points (CCP's)</p><p>• Conducts all duties in compliance with safety rules, applicable SOPs, and other applicable guidelines.</p><p>• Conduct inspections and audits with state and local regulatory and law enforcement agencies</p><p>• Collect, audit, and file required operational logs from all departments to ensure compliance</p><p>• Collect and file all signed transfer manifests</p><p>• Regulatory research and summarizations</p><p>• Prepare monthly cultivation and inventory inspection reports</p><p>• Monitor inventory losses and assist in developing processes and procedures to reduce loss in all departments</p><p>• Ensure full inventory is completed in all departments and investigate/ resolve any inventory discrepancies</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>• Bachelor's degree (in Food Science, Agriculture, Biology, Microbiology, or Chemistry preferred)</p><p>• 5+ years' experience in a Quality and/or Compliance role</p><p>• Must be HACCP Certified</p><p>• Must be Certified in Internal Auditing</p><p>• Must be PCQI Certified</p><p>• Prior experience in highly regulated industry: healthcare, medical devices, pharmaceutical, consumer packaged goods (food), cannabis, tobacco, dietary supplements, cosmetics, OTC, or personal Care</p><p>• Highly desirable: FDA, HACCP, GFSI (Global Food Safety Initiative) such as BRC, SQF, and FSSC 22000</p><p>• Prior experience with product sampling, inspection procedures, customer complaints, product investigations, and CAPA</p><p>• Prior experience in regulatory agency inspections/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>• Must be detail-oriented</p><p>• Strong analytical skills, including working knowledge of microbiology, chemistry and technical data</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":"Stuart, FL, USA","city":"Stuart","stateProvince":"FL"},"frontendLink":"/job-posting/cresco-labs/quality-manager/db246675bcb879cd8bb9af5f6a678370","title":"Quality Manager","hash":"db246675bcb879cd8bb9af5f6a678370","postingUrl":"https://www.themuse.com/jobs/crescolabs/quality-manager-18c375"},{"employmentType":"Full-time","postedOn":"21 days ago","description":"<div><p>Operational Quality Manager Job at Tidal Health Solutions Ltd. – Saint Stephen, NB</p><p><b>Position Summary:</b></p><p>The Operational Quality Manager is primarily responsible for ensuring the quality and efficacy of Tidal Operations under the Cannabis Act. The incumbent will work closely with the Director of Regulatory Compliance to ensure Department meets and exceeds quality requirements in production of Cannabis 2.0 products.</p><p><b>Responsibilities:</b></p><p>• Supervise the Quality Control (QC) team.</p><p>• Develop, implement and maintain a GMP Plan.</p><p>• Develop, implement and oversee projects to increase production efficiency while being cognizant to simultaneously improve Tidals’ organization structure.</p><p>• Oversee master batch record, certificates of analysis and issuance of certificates of conformance for all approved products including review of results and any necessary actions for deviations and change controls.</p><p>• Lead CAPA program to ensure appropriate response to deviation, non-conformance or audit deficiencies.</p><p>• Develop stability protocols and analyze results.</p><p>• Support Health Canada and CRA audits as necessary.</p><p>• Inventory management of cannabis products.</p><p>• Develop and implement a lot traceability program from raw materials to finished goods.</p><p>• Review all purchase order requests from Quality team for approval.</p><p>• Complete post approval finished goods specifications as required.</p><p>• Manage document control program including document creation, review and publishing</p><p>• Enforce Good Document Practices on all applicable documents.</p><p>In conjunction with Director, Regulatory Compliance</p><p>• Final batch review and release.</p><p>• Define and execute short and long-term strategic initiatives to ensure quality and regulatory compliance.</p><p>• Oversee the development, implementation and management of quality programs and policies, including adherence to the Cannabis Act, CRA and regulatory requirements.</p><p>• Supervise and develop the Quality team to identify and achieve optimum performance, best practices, technical capabilities, career development and personal growth.</p><p>• Review investigations and reports for quality related incidents (customer complaints, mock recalls, foreign materials, etc.)</p><p>• Liaise with Joint Health &amp; Safety Committee to ensure compliance with Occupational Health and Safety Act in all Tidal activities</p><p><b>Qualifications:</b></p><p>• Bachelor’s Degree in biological sciences or related field of study.</p><p>• Relevant industry certification (HACCP, WHIMIS, SQF, etc.)</p><p>• Audit and recall experience.</p><p>• A minimum of 3 years’ experience in pharmaceutical or food manufacturing as a QA manager.</p><p>• Thorough understanding of the Cannabis Act and other relevant regulations. Must currently hold or qualify to obtain the level of security clearance per Health Canada regulations.</p><p>• Our ideal candidate is an experienced team leader with a positive attitude, strong analytical abilities, high attention to detail and high accuracy in record keeping, as well as a vision for the future of Tidal.</p><p>Application deadline: 2021-09-27</p><p>Expected start date: 2021-10-18</p><p>Job Types: Full-time, Permanent</p><p><b>Benefits:</b></p><p>• Dental care</p><p>• Disability insurance</p><p>• Extended health care</p><p>• Life insurance</p><p>• Store discount</p><p>• Vision care</p><p><b>Schedule:</b></p><p>• 8 hour shift</p><p>• Monday to Friday</p><p><b>COVID-19 considerations:</b></p><p>Tidal Health Solutions follows all Public Health guidelines in reference to COVID19.</p><p><b>Work remotely:</b></p><p>About the Company</p><p>Company: Tidal Health Solutions Ltd. –</p><p>Company Location: Saint Stephen, NB</p><p>Estimated Salary</p></div>","company":{"website":"tidalhealth.ca","companyType":"Private/Growth","name":"Tidal Health Solutions Ltd.","logoUrl":"/logos/tidal-health-solutions-ltd-54b2c39bf898a132bb122e791a36a861.jpeg"},"location":{"country":"Canada","address":"Saint Stephen, NB","city":"Saint Stephen","stateProvince":"NB"},"frontendLink":"/job-posting/tidal-health-solutions-ltd/operational-quality-manager/d5cc6300675f6a536fe92a31adc1f17c","title":"Operational Quality Manager","hash":"d5cc6300675f6a536fe92a31adc1f17c","postingUrl":"https://qajobshub.com/job/operational-quality-manager-3/"},{"postedOn":"4 days ago","description":"<div><div><b>PHM Brands</b><br /><br /><b>TITLE:</b> Quality Assurance Manager<br /><br /><b>LOCATION:</b> Champaign, IL<br /><br /><b>DATE POSTED:</b> 9/13/2021<br /><br /><b>SALARY:</b> Based on Experience<br /><br /><b>DESCRIPTION:</b> The Quality Assurance Manager is responsible for providing leadership to the quality assurance team and manages all food/product safety, quality programs, and laboratory activities of the facility. Manage and oversee the entire plant's food safety and quality control functions consistent with FSMA requirements, GFSI standards, Food Safety principles, allergen controls and GMP practices. Review raw material and finished products for compliance to regulation and specification. Active leader in ensuring all aspects of the plant' s Food Safety programs and Regulatory Compliance are maintained to the highest standards. Participate in ongoing review and evaluation of the plant' s GFSI program as a GFSI Leader and assist in employee training of GFSI principles and pre-requisite programs. Manage and oversee daily laboratory functions, Sanitation and Pest Control activities. The Quality Assurance Manager will be based out of Monticello, IL.<br /><br /><b>QUALIFICATIONS:</b><br /><ul><li>Bachelor's Degree in Food Science or equivalent experience, food process engineering, or appropriate biological sciences. Certified in a GFSI Scheme a plus.</li><li>Three to five (3-5) years of professional work-related experience in quality assurance and or quality control and food safety out of the food industry.</li><li>Previous experience in the CBD industry preferred, but not required.</li><li>Preventative Controls for Food Safety Qualified Individual (PCQI Certified).</li><li>Three years to five years' experience with HACCP / Quality Assurance Programs.</li><li>Ability to manage an hourly staff and interface with various levels of Management.</li><li>Ability to read, analyze, and interpret general food industry periodicals, professional journals and government regulations.</li><li>Ability to produce reports, business correspondence and procedure Read, write, and speak English fluently.</li><li>Intermediate or above knowledge of Microsoft Word, Excel, and PowerPoint software programs. Proficient in use of various \"mainframe\" data management systems and</li><li>Ability to resolve practical problems and deal with a variety of variables.</li><li>Ability to interpret a variety of instructions furnished in written, oral, diagram or schedule</li><li>Ability to calculate figures, analyze financial reports, determine processing rates work with percentages and fractional calculations.</li><li>Strong knowledge of Food GMP's, SOP's, HACCP/Food Safety, CBD, Regulatory and Environmental</li><li>Experience with Organic, Kosher, and API (Active Pharmaceutical Ingredient) certification and</li><li>Ability to meet attendance</li><li>Ability to maintain an effective working relationship with all internal and external contacts.</li><li>Understanding of basic principles of the GFSI programs and other food safety policies/procedures.</li><br /><b>PHYSICAL DEMANDS:</b><br /><ul><li>Rotating and oscillating equipment</li><li>Exposure to manufacturing equipment hazards, especially forklifts</li><li>Standing and walking on concrete floor</li><li>Exposure to raw hemp biomass</li><br /><b>BENEFIT SUMMARY:</b><br /><br />Medical, Dental, Vision, Company Paid LI, AD&amp;D, Matching 401K, Employee Assistance Program, Paid Time off<br /><br />PHM Brandsis an equal opportunity employer and considers qualified applicants for employment without regard to sex, race, color, religion, ethnic or national origin, gender, sexual orientation, gender identity or expression, age, pregnancy, leave status, disability, veteran status, genetic information and/or any other characteristic or status protected by national, federal, state, or local law.<br /><br />PM21</ul></ul><p><br />PI147201849</p></div></div>","company":{"companyType":"Private/Established","name":"PHM Brands","logoUrl":"/logos/phm-brands-llc-871151ce94e5c9812b99a6fbd0d48599.png"},"location":{"country":"United States","address":"Champaign, IL 61820","city":"Champaign","stateProvince":"IL"},"frontendLink":"/job-posting/phm-brands/quality-assurance-manager/80dd458f3e7fc0eb4f21b862d3760af8","title":"Quality Assurance Manager","hash":"80dd458f3e7fc0eb4f21b862d3760af8","postingUrl":"https://www.indeed.com/job/quality-assurance-manager-44794ff0b4c24c5e"},{"employmentType":"Full-time","postedOn":"9 days ago","description":"<div><p>Job DescriptionMedical Saints is a licensed cannabis and hemp producer proudly rooted in the province of Ontario. We’re on a mission to become Canada’s most reliable producer of premium cannabis and hemp. We pride ourselves on pharmaceutical-grade reliability, small batch quality and unmatched genetic diversity. Each year, Medical Saints harvests over 100,000 kgs of quality cannabis and hemp using a hybrid approach of high-tech automation and meticulous human care. We have three branches dispersed throughout Ontario.The Niagara branch, located in Beamsville Ontario, is the 350,000 sqft. powerhouse of the Medical Saints operation. Each year, our Niagara Branch will yield 50,000 kgs of sun-grown cannabis. Our greenhouse is automated with cutting-edge technology to guarantee consistency across each and every harvest. Our team maintains an environment for pharma-grade cultivation and meticulously assesses the quality of each harvest. This branch has recently been awarded a cultivation license.Opportunity: - Review and maintain batch records- Perform production in-proces spot checks- Perform weekly compliance checks on facility- Conduct ongoing training on SOPs- Participte in authoring SOPs- Participate in internal and external audits- Participate in CAPA and Deviation investigations and reporting- Gather product and material samples from around facility and coordinate sending samples for testing- Assist with customer complaints and recall program- Take and maintain retention samples- Provide support for cannabis destruction programRequirements: - Experience in Quality Assurance in food, pharma, cannabis or related industry- Post secondary education in a technical field is required (microbiology or chemistry preferred, related science excepted)- Familiarity with Health Canada Cannabis regulations- Experience in implementation of HACCP, ISO, GMP and/or GPP- Detail oriented individual with strong communication and conflict management skills- Strong problem solving and critical thinking skills are an asset- Ability to proficiently use Microsoft office applications- Ability to acquire a valid security clearanceCompany DescriptionMedical Saints is a licensed cannabis and hemp producer proudly rooted in the province of Ontario. We’re on a mission to become Canada’s most reliable producer of premium cannabis and hemp. We pride ourselves on pharmaceutical-grade reliability, small batch quality and unmatched genetic diversity. Each year, Medical Saints harvests over 100,000 kgs of quality cannabis and hemp using a hybrid approach of high-tech automation and meticulous human care. We have three branches dispersed throughout Ontario.The Niagara branch, located in Beamsville Ontario, is the 350,000 sqft. powerhouse of the Medical Saints operation. Each year, our Niagara Branch will yield 50,000 kgs of sun-grown cannabis. Our greenhouse is automated with cutting-edge technology to guarantee consistency across each and every harvest. Our team maintains an environment for pharma-grade cultivation and meticulously assesses the quality of each harvest. This branch has recently been awarded a cultivation license</p></div>","company":{"name":"Medical Saints Ltd"},"location":{"country":"Canada","address":"Canada"},"frontendLink":"/job-posting/medical-saints-ltd/quality-assurance-manager/66573b0d2e40bdd16dcf95691e3876b6","title":"Quality Assurance Manager","hash":"66573b0d2e40bdd16dcf95691e3876b6","postingUrl":"https://ca.trabajo.org/job-649-20210913-582338abb35e4d0b407b9ee668ff017a"},{"employmentType":"Full-time","postedOn":"10 days ago","description":"<div><p><b>Job Description</b></p><p>Medical Saints is a licensed cannabis and hemp producer proudly rooted in the province of Ontario. We’re on a mission to become Canada’s most reliable producer of premium cannabis and hemp. We pride ourselves on pharmaceutical-grade reliability, small batch quality and unmatched genetic diversity. Each year, Medical Saints harvests over 100,000 kgs of quality cannabis and hemp using a hybrid approach of high-tech automation and meticulous human care. We have three branches dispersed throughout Ontario.</p><p>The Niagara branch, located in Beamsville Ontario, is the 350,000 sqft. powerhouse of the Medical Saints operation. Each year, our Niagara Branch will yield 50,000 kgs of sun-grown cannabis. Our greenhouse is automated with cutting-edge technology to guarantee consistency across each and every harvest. Our team maintains an environment for pharma-grade cultivation and meticulously assesses the quality of each harvest. This branch has recently been awarded a cultivation license.</p><p><b>Opportunity:</b></p><p>- Review and maintain batch records</p><p>- Perform production in-proces spot checks</p><p>- Perform weekly compliance checks on facility</p><p>- Conduct ongoing training on SOPs</p><p>- Participte in authoring SOPs</p><p>- Participate in internal and external audits</p><p>- Participate in CAPA and Deviation investigations and reporting</p><p>- Gather product and material samples from around facility and coordinate sending samples for testing</p><p>- Assist with customer complaints and recall program</p><p>- Take and maintain retention samples</p><p>- Provide support for cannabis destruction program</p><p><b>Requirements:</b></p><p>- Experience in Quality Assurance in food, pharma, cannabis or related industry</p><p>- Post secondary education in a technical field is required (microbiology or chemistry preferred, related science excepted)</p><p>- Familiarity with Health Canada Cannabis regulations</p><p>- Experience in implementation of HACCP, ISO, GMP and/or GPP</p><p>- Detail oriented individual with strong communication and conflict management skills</p><p>- Strong problem solving and critical thinking skills are an asset</p><p>- Ability to proficiently use Microsoft office applications</p><p>- Ability to acquire a valid security clearance</p><p>Company Description</p><p>Medical Saints is a licensed cannabis and hemp producer proudly rooted in the province of Ontario. We’re on a mission to become Canada’s most reliable producer of premium cannabis and hemp. We pride ourselves on pharmaceutical-grade reliability, small batch quality and unmatched genetic diversity. Each year, Medical Saints harvests over 100,000 kgs of quality cannabis and hemp using a hybrid approach of high-tech automation and meticulous human care. We have three branches dispersed throughout Ontario.</p><p>The Niagara branch, located in Beamsville Ontario, is the 350,000 sqft. powerhouse of the Medical Saints operation. Each year, our Niagara Branch will yield 50,000 kgs of sun-grown cannabis. Our greenhouse is automated with cutting-edge technology to guarantee consistency across each and every harvest. Our team maintains an environment for pharma-grade cultivation and meticulously assesses the quality of each harvest. This branch has recently been awarded a cultivation license</p></div>","company":{"name":"Medical Saints Ltd"},"location":{"country":"Canada","address":"Beamsville, ON","city":"Beamsville","stateProvince":"ON"},"frontendLink":"/job-posting/medical-saints-ltd/quality-assurance-manager/8e597791cb9065af17d0964fbb9e85b4","title":"Quality Assurance Manager","hash":"8e597791cb9065af17d0964fbb9e85b4","postingUrl":"https://en-ca.whatjobs.com/jobs/Quality-Assurance-Associate/Beamsville/14020834"},{"employmentType":"Full-time","postedOn":"14 days ago","description":"<div><p><b>Overview</b></p><p>Reporting to the Manager, Quality Assurance, the Quality Assurance Manager will assist in developing and maintaining the Quality Management System to support the organization’s business operations and manufacturing process in compliance with the Cannabis Act. The QA Manager will work in a fast-paced and growth-</p><p>oriented environment and be able to adapt to changing business needs while performing a variety of tasks.</p><p>What can you expect to do</p><p>• Development, implementation, enforcement and continuous monitoring of the quality assurance systems and KPI’s in strict compliance with the Cannabis Act and internal procedures.</p><p>• Coordinate and investigate all quality issues such as Out Of Specification (OOS), complaints, deviations, returns and</p><p>• Initiate, implement and close corrective and preventive actions in a timely</p><p>• Attend and coordinate regular and targeted Health Canada inspections, as well as other external audits and internal</p><p>• Ensure proper control, release and transfer of incoming and outgoing materials for production and sale in a timely</p><p>• Perform in-house testing and sampling as required and coordinate external testing of materials/products as per approved</p><p>• Oversee and verify that the various processes and records are completed as specified to be fully compliant, g. sanitation program, waste destruction, room/equipment inspection etc.</p><p>• Develop, review and maintain Standard Operating Procedures (SOPs).</p><p>• Train staff in SOPs to ensure the effective implementation of quality policies and procedures and oversee the training</p><p>• Propose and implement new initiatives for continuous improvement of the quality system, provide support and guidance for new</p><p>• Coordinate and approve qualification / validation</p><p>• Hire staff, establish objectives, monitor staff performance and support their development</p><p>• Other duties as</p><p>What we are looking for</p><p>• Bachelor's degree in Chemistry, Microbiology or equivalent experience in a related field and minimum 5 years’ relevant experience within a highly regulated industry (pharmaceutical, biotech or cannabis).</p><p>• Experience in cannabis sector and knowledge of the Cannabis Act is a definite</p><p>• Experience in drafting standard operating procedures, validation reports, reviewing manufacturing and quality</p><p>• Ability to gather, summarize, and interpret complex analytical and quality</p><p>• Strong root cause analysis and investigative</p><p>• Detail oriented with strong organizational</p><p>• Ability to work independently, adapt rapidly to changing</p><p>• Able to manage and coordinate multiple projects</p><p>• Ability to collaborate productively and efficiently with multiple internal and external</p><p>• Strong management and leadership skills along with strategic thinking and decision-making ability and a proven track record of regulatory</p></div>","company":{"website":"auxly.com","companyType":"Private/Growth","name":"Auxly Cannabis Group","logoUrl":"/logos/auxly-cannabis-group-inc-56917990efed42457bbac5214a4a8b4d.jpeg"},"location":{"country":"Canada","address":"Carleton Place, ON","city":"Carleton Place","stateProvince":"ON"},"frontendLink":"/job-posting/auxly-cannabis-group/quality-assurance-manager/71096fa117e5cdb0d2e814872377ea6a","title":"Quality Assurance Manager","hash":"71096fa117e5cdb0d2e814872377ea6a","postingUrl":"https://www.theladders.com/job/quality-assurance-manager-auxly-cannabis-group-carleton-place-on_48115391"},{"employmentType":"Full-time","postedOn":"20 days ago","description":"<div><p>Full-time 3 hours ago Full Job Description The Quality Assurance Manager will maintain the quality standards set by gLeaf as well as oversee regulatory standards set by each facility's governing body. Essential Duties and Responsibilities: Run and manage a QA lab that is responsible for internal testing of microbial, pesticide, or any other form of contamination in our biomass and finished products. o PCR, Plating, HPLC, etc. Run and manage equipment that tracks biomass and finished product cannabinoid potency and terpene content. Maintain plant genetics in a deep tissue culture lab under the direction of DOO and DOC. Work with director and manager level production operations personnel to develop and maintain GMP standards and practices. Routinely test and calibrate production machines and equipment. Assist in the R&amp;D of grow and extraction practices. Work with compliance and safety personnel to ensure safe and compliant handling of all potentially hazardous material in production facilities. Education: High School Diploma or General Education Degree (GED) required. Experience: 2 years of grow and extraction experience 1 year of compliance and safety related experience Skills: Strong ability to lead and motivate employees Strong attention to detail Ability to clean and stabilize genetics Strong organization skills Strong knowledge of state regulations and compliance practices Ability to handle potentially hazardous material Physical Requirements: Must be able to lift 25 pounds Must be able to stand for long periods of time Must be able to perform data entry for extended periods of time Green Leaf (gLeaf) is a multi-state, vertically integrated operation, leading the cannabis industry in the production and sales of high quality medicine. We currently have an exciting opportunity for a talented and passionate Quality Assurance Manager to join our team! The current opening is for our Saxton Cultivation Facility but can be available at our Richmond, VA or Frederick, MD locations. Salary will commensurate with candidate experience. Location: 135 Horton Drive, Saxton, PA 16678 Job Type: Full-time</p></div>","company":{"companyType":"Growth","name":"Green Leaf Medicals, LLC"},"location":{"country":"United States","address":"Saxton, PA, USA","city":"Saxton","stateProvince":"PA"},"frontendLink":"/job-posting/green-leaf-medicals-llc/quality-assurance-manager/4cbbc075e0b211ed2da3d36aa4cb284a","title":"Quality Assurance Manager","hash":"4cbbc075e0b211ed2da3d36aa4cb284a","postingUrl":"https://saxton-pa.geebo.com/jobs-online/view/id/911970773-quality-assurance-manager-/"},{"employmentType":"Full-time","postedOn":"20 days ago","description":"<div><p>GVB Biopharma is a vertically integrated, global leader in the ever-growing hemp industry. GVB operates two state-of-the-art facilities: a 30,000-square-foot food-grade hemp processing facility in Central Oregon and a 40,000-square-foot white-label consumer product manufacturing facility in Las Vegas, Nevada. GVB also has sales and general administrative offices in California and Colorado.</p><p>Job Summary: This position requires the ability to lead and train Quality professionals in the appropriate application of standards including ISO 9001:2015 and cGMP and support both internal and external customers.<br />Primary responsibilities include:</p><ul><li>Leads in the development of a climate of quality and safety, seeking continuous improvement, providing sound vision and guidance in the application of Quality standards</li><li>Administrate and manage the Quality Management System, driving to completion events such as corrective actions, change control, deviations, nonconforming product, and audit reports</li><li>Aid in determining root cause for nonconforming events and evaluate corrective and preventive actions for lifecycle effectiveness</li><li>Author or approve key Quality System documents</li><li>Author, approve and defend as applicable corrective actions</li><li>Effectiveness monitoring of site Quality Systems, presenting during the management review cycle</li><li>Assist and support Audit Program to evaluate compliance requirements and identify areas requiring corrective action or opportunities for improvement</li><li>Assure timely completion of corrective and preventive actions</li><li>Maintain and support procedures to ensure the compliance of all products and packaging</li><li>Support supplier approval program, setting requirements for raw material and component products and tracking supplier compliance</li><li>Oversee product development procedures to identify deviations from quality standards</li><li>Product stability study coordination</li><li>Supervise direct reports, providing guidance and feedback</li><li>Execute and manage processes to ensure effective documentation control</li><li>Recall and mock recall coordination</li></ul><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></ul><p>Supplemental Pay:</p><ul><li>Bonus pay</li></ul><p>COVID-19 considerations:<br />GVB has measures and regulations in place to ensure the health and wellbeing of our employees. We have established social distancing and mask requirements and have been following all state and local regulations.</p><ul><li>Bachelor’s degree in chemistry, biology, or related field with seven years of professional experience in the pharmaceutical, dietary supplement, or food industry, preferably with five years in a Quality role</li><li>Supervisory or management experience</li><li>ASQ certified CMQ/OE, CQE, CQA, or CFSQA</li><li>Proficient skills in, G Suite, Video Conferencing, Excel, and Word</li><li>Strong organizational skills and the ability to work effectively with a team</li></ul><p>Location: 212 NORTH STREET, Grass Valley, OR 97029</p><p>Job Type: Full-time</p></div>","company":{"companyType":"Private/Startup","name":"Evergreen State Holdings Llc","logoUrl":"/logos/evergreen-state-holdings-llc-472c5fa08bad68be7418ef3aeb015236.png"},"location":{"country":"United States","address":"Grass Valley, OR 97029","city":"Grass Valley","stateProvince":"OR"},"frontendLink":"/job-posting/evergreen-state-holdings-llc/quality-assurance-manager/cdf92d9de1128e2944558a00ef5fce30","title":"Quality Assurance Manager","hash":"cdf92d9de1128e2944558a00ef5fce30","postingUrl":"https://www.indeed.com/job/quality-assurance-manager-78d96452f4c5041e"},{"employmentType":"Full-time","postedOn":"22 days ago","description":"<div><p>AWH is a vertically integrated cannabis cultivator, processor and dispensary operator with assets in Illinois, Massachusetts Michigan and Ohio. We seek to foster a robust and inclusive cannabis organization through providing a premium, unmatched customer-focused retail experience and producing quality and mindfully created cannabis products. Our goal is to build a world class team that will continue our mission of helping to shape the future of cannabis and bettering our customers life with cannabis. How will we achieve this? By offering unrivaled quality, consistency and meticulously curated products that satisfy our customers unique, individual needs.</p><p>When it comes to customer service experience, our dispensaries will set a new standard of excellence, emphasizing health and wellness. As a team that is committed to our values, our people and our communities; we are looking for people who are inspired by our vision and stay dedicated to our mission as we scale continuously.</p><p>Why AWH?</p><p>Our people are our greatest asset. Our teams are comprised of a group of skilled and passionate professionals and partners from a diverse range of fields. We believe in not only building a diverse team but creating a space where ALL feel welcome and training our leaders to not only be inclusive themselves but to inspire their teams to be the same. We provide equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, gender, gender identity, national origin, age or disability. We believe in providing competitive compensation, quality benefits and a work environment that fosters creativity, hard work and leverage every one of our employees' unique skills while giving them what it takes to advance those said skills and learn new ones. We sweat the details to ensure our teams are confident and excited to provide best in class service to our customers and communities we serve.</p><p>The Quality Assurance Manager is responsible for monitoring and evaluating internal production processes, overseeing quality-related activities at the facility associated with sampling and inspection of in-process and finished products, customer complaints, product investigations, and Corrective and Prevention Action (CAPA) plans. The Quality Assurance Manager 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. The Quality Assurance Manager reports directly to the site leader.</p><p><b>Essential Duties and Responsibilities</b></p><p>• Monitoring and evaluating internal production processes.</p><p>• Responsible for developing product quality safety and sanitation programs for the cultivation site.</p><p>• Build a documented consumer complaint process complete with trending, weekly reviews and trend reduction.</p><p>• Create guidance in regulations consistent with FSMA, CGMP and food CFR requirements.</p><p>• Assurance of sound raw and FG traceability program.</p><p>• Development of Master Sanitation program.</p><p>• Implementation of thorough line quality measurement systems.</p><p>• Documentation and control of all processes.</p><p>• Lead a strong pest control program.</p><p>• Developing quality control processes and design product specifications.</p><p>• Supervising staff and monitoring production standards.</p><p>• Examining the quality of raw/pack materials that are used in production.</p><p>• Evaluating the final output of products to determine their quality.</p><p>• Producing statistical reports on quality standards.</p><p>• Rejecting products that fail quality standards.</p><p>• Implement HACCP program all within the food work streams.</p><p>Supervisory Responsibilities</p><p>• This position has no supervisory responsibilities at this time but will require engagement and accountability by managers involved in the daily operations of the facility.</p><p><b>Competencies</b></p><p>• Treat people with respect, keeps commitments, inspires the trust of others, works with integrity and ethically, upholds organizational values.</p><p>• Is consistently at work and on time, ensures work responsibilities are covered when absent, arrives at meetings and appointments on time.</p><p>• Observes and adheres to regulatory, safety and security procedures.</p><p>• Ability to maintain a 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-driven environment while successfully managing multiple tasks.</p><p>Requirements and Qualifications</p><p>• 2 year degree in Business Administration, or relevant field. 4 year degree preferred.</p><p>• Quality Control Certification preferred.</p><p>• Minimum 3 – 5 years as a Site Quality Manager; strong food experience is a plus</p><p>• Ability to build and manage external auditing such as SQF or BRC initiatives.</p><p>• Lean manufacturing experience and HACCP certified a plus.</p><p>• Advanced CAPA, RCA, and strategic planning experience</p><p>• Advanced experience conducting audits, data analysis and reporting statistics.</p><p>• Highly computer literate and proficient in MS Office including Excel, PowerPoint, Word and data analytics.</p><p>• Excellent critical thinking and problem-solving skills.</p><p>• Excellent interpersonal and communication skills including speaking and writing.</p><p>• Proven track record in people leadership (supporting, developing, engaging) with demonstrated teambuilding and collaboration skills.</p><p>• Must​ ​be​ ​a​t least ​21​ ​years​ ​of​ ​age.</p><p>• Must​ ​pass​ ​any​ ​and​ ​all​ ​required​ ​background​ ​checks.</p><p>• Must​ ​be​ ​and​ ​remain​ ​compliant​ ​with​ ​any​ ​and​ ​all​ ​regulatory requirements​ ​for​ ​working​ ​in​ ​the cannabis industry.</p><p>• Must​ be able to ​obtain​ ​and​ ​retain​ ​a​ ​Registered Agent Card issued by the MA Cannabis Control Commission.</p><p>• Must have excellent organization and time management skills.</p><p>• Must be focused, pay close attention to detail and accuracy of data recorded.</p><p>• Must be able to internalize training and ​follow instructions consistently.</p><p>• Must be able to work effectively as part of a team and grow with the company</p><p><b>Work Environment</b></p><p>This position performs duties in an agricultural/manufacturing environment</p></div>","company":{"website":"awholdings.com","name":"Ascend Wellness"},"location":{"country":"United States","address":"Lansing, MI, USA","city":"Lansing","stateProvince":"MI"},"frontendLink":"/job-posting/ascend-wellness/quality-assurance-manager/6fdecb7315ce03e80979620fcf9fc2eb","title":"Quality Assurance Manager","hash":"6fdecb7315ce03e80979620fcf9fc2eb","postingUrl":"https://www.theladders.com/job/quality-assurance-manager-ascendwellness-lansing-mi_47988890"},{"postedOn":"17 days ago","description":"<div>AQAP Job Description<br /><br />The Alternate Quality Assurance Person is a security cleared position that is responsible for the managing of all quality assurance processes for the cultivation site ( indoor and outdoor) . This is a full time on site position for a License Holder in Sudbury.<br /><br />This role is responsible for ensuring that all Quality processes are maintained at the highest level, that we are following our Standard Operating Procedures (SOPs) and meeting company expectations.<br /><br />Job Duties<br /><ul><li>Provides leadership and expertise for total quality management</li><li>Create an auditing system that ensures SOPs are strictly followed</li><li>Train staff in SOPs to ensure the correct implementation in operations and regulatory compliance</li><li>Perform relevant cannabis product tests and ensure that products are not released for sale until their quality has been determined to meet their specific qualifications.</li><li>Understand and implement all necessary Quality Assurance Systems</li><li>Establish quality management systems and risk management within cannabis companies for better performance</li><li>Design self-inspection and regulatory inspection methods for cannabis operation</li><li>Review and approve Certificate of Analysis</li><li>Develop cannabis technical procedures</li><li>Provide leadership on QA and QMS systems and all regulatory requirements protocols</li><li>Perform internal Quality Assurance (QA) audits that are compliant with corporate policies, practices and procedures</li><li>Maintain QA control documentation</li><li>Identify relevant QA training needs and opportunities</li><li>Conduct tests and create reports in compliance with policies and SOPs</li><li>Conduct risk analysis, verification, validation activities, and formal design reviews as needed</li><li>Ensure that refuse and cannabis products are managed or destroyed in accordance with the Cannabis Act</li><li>Complete inspection reports on production equipment, sanitation practices, and production areas</li><li>Review complaints and follow up with appropriate departments</li><li>Create NCR reports, deviations reports and recall simulation reports</li><li>Recommend corrective action where needed</li><li>Other duties as required</li></ul>Requirements<br /><ul><li>Minimum Bachelor’s Degree in Biological Sciences/Pharmacy/Food or post-secondary diploma in a Science-related technical discipline</li><li>Security clearance is a requirement</li><li>Minimum of 2+ years experience as a AQAP</li><li>Must possess a passion for cannabis industry in general, while providing excellent regulatory advice in line with the current regulations</li><li>Experience with Ample Organics Seed to Sale Software is an asset</li><li>Proficient in MS Office Suite software (Excel, Outlook, Word, SharePoint) and ability to adapt to new technology</li><li>Strong understanding of Cannabis Act and Regulations, and ability to apply the same designing and updating of polices and procedures</li></ul></div>","company":{"companyType":"Private/Startup","name":"Seale and Garland Consulting Inc.","logoUrl":"/logos/seale-and-garland-consulting-inc-1a43537258d7c2221de6ae1aca668bd7.jpeg"},"location":{"country":"Canada","address":"Greater Sudbury, ON","city":"Greater Sudbury","stateProvince":"ON"},"frontendLink":"/job-posting/seale-and-garland-consulting-inc/alternate-quality-assurance-manager/0ef39f007d34c52708d4b4fd57aa244e","title":"Alternate Quality Assurance Manager","hash":"0ef39f007d34c52708d4b4fd57aa244e","postingUrl":"https://ca.indeed.com/job/alternate-quality-assurance-manager-ea96b6d737178abb"},{"employmentType":"Full-time","postedOn":"25 days ago","description":"<div><p>GVB Biopharma is an industry-leading, vertically integrated global leader in the ever-growing hemp industry. We prioritize cannabinoid research, industry innovation, and traceable quality control. GVB operates two state-of-the-art facilities: a 30,000-square-foot food-grade hemp processing facility in Central Oregon and a 40,000-square-foot white-label consumer product manufacturing facility in Las Vegas.</p><p>JOB SUMMARY:<br />This position requires the ability to lead and train Quality professionals in the<br />appropriate application of standards including ISO 9001:2015 and cGMP and support both internal and external customers.</p><p>ESSENTIAL DUTIES AND RESPONSIBILITIES.</p><p>*Other assignments, projects, and duties may be required:</p><p>Primary responsibilities include:</p><ul><li>Leads in the development of a climate of quality and safety, seeking continuous</li></ul><p>improvement, providing sound vision and guidance in the application of Quality standards</p><ul><li>Administrate and manage the Quality Management System, driving to completion events such as corrective actions, change control, deviations, nonconforming product, and audit reports</li><li>Aid in determining root cause for nonconforming events and evaluate corrective and preventive actions for lifecycle effectiveness</li><li>Author or approve key Quality System documents</li><li>Author, approve and defend as applicable corrective actions</li><li>Effectiveness monitoring of site Quality Systems, presenting during the management review cycle</li><li>Assist and support Audit Program to evaluate compliance requirements and identify areas requiring corrective action or opportunities for improvement</li><li>Assure timely completion of corrective and preventive actions</li><li>Maintain and support procedures to ensure the compliance of all products and packaging</li><li>Support supplier approval program, setting requirements for raw material and component products and tracking supplier compliance</li><li>Oversee product development procedures to identify deviations from quality standards</li><li>Product stability study coordination</li><li>Supervise direct reports, providing guidance and feedback</li><li>Execute and manage processes to ensure effective documentation control</li><li>Recall and mock recall coordination</li></ul><p>PREFERRED QUALIFICATIONS:</p><ul><li>Bachelor’s degree in chemistry, biology, or related field with seven years of professional experience in the pharmaceutical, dietary supplement, or food industry, preferably with five years in a Quality role</li><li>Supervisory or management experience</li><li>ASQ certified CMQ/OE, CQE, CQA, or CFSQA</li><li>Proficient skills in, G Suite, Video Conferencing, Excel, and Word</li><li>Strong organizational skills and the ability to work effectively with a team</li></ul><p>Job Type: Full-time</p><p>Pay: $75,000.00 - $85,000.00 per year</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></ul><p>Supplemental Pay:</p><ul><li>Bonus pay</li></ul><p>COVID-19 considerations:<br />GVB has measures and regulations in place to ensure the health and wellbeing of our employees. We have established social distancing and mask requirements and have been following all state and local regulations.</p><p>Application Question(s):</p><ul><li>Please list any relevant certifications as required by the Job Description.</li><li>Our facility is located in Grass Valley, OR. Are you willing and or able to commute/relocate to Grass Valley?</li></ul><p>Education:</p><ul><li>Bachelor's (Preferred)</li></ul><p>Experience:</p><ul><li>Quality Assurance: 5 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":"GVB Biopharma","logoUrl":"/logos/gvb-biopharma-ec55e466c36a12bccf78758e67009397.jpeg"},"location":{"country":"United States","address":"Oregon","stateProvince":"OR"},"frontendLink":"/job-posting/gvb-biopharma/quality-assurance-manager/16cdfbcb536fa21fcb7a402c28418bec","title":"Quality Assurance Manager","hash":"16cdfbcb536fa21fcb7a402c28418bec","postingUrl":"https://www.indeed.com/job/quality-assurance-manager-e86ce8785fd64f53"},{"employmentType":"Full-time","postedOn":"25 days ago","description":"<div><p>GVB Biopharma is an industry-leading, vertically integrated global leader in the ever-growing hemp industry. We prioritize cannabinoid research, industry innovation, and traceable quality control. GVB operates two state-of-the-art facilities: a 30,000-square-foot food-grade hemp processing facility in Central Oregon and a 40,000-square-foot white-label consumer product manufacturing facility in Las Vegas.</p><p>JOB SUMMARY:<br />This position requires the ability to lead and train Quality professionals in the<br />appropriate application of standards including ISO 9001:2015 and cGMP and support both internal and external customers.</p><p>ESSENTIAL DUTIES AND RESPONSIBILITIES.</p><p>*Other assignments, projects, and duties may be required:</p><p>Primary responsibilities include:</p><ul><li>Leads in the development of a climate of quality and safety, seeking continuous</li></ul><p>improvement, providing sound vision and guidance in the application of Quality standards</p><ul><li>Administrate and manage the Quality Management System, driving to completion events such as corrective actions, change control, deviations, nonconforming product, and audit reports</li><li>Aid in determining root cause for nonconforming events and evaluate corrective and preventive actions for lifecycle effectiveness</li><li>Author or approve key Quality System documents</li><li>Author, approve and defend as applicable corrective actions</li><li>Effectiveness monitoring of site Quality Systems, presenting during the management review cycle</li><li>Assist and support Audit Program to evaluate compliance requirements and identify areas requiring corrective action or opportunities for improvement</li><li>Assure timely completion of corrective and preventive actions</li><li>Maintain and support procedures to ensure the compliance of all products and packaging</li><li>Support supplier approval program, setting requirements for raw material and component products and tracking supplier compliance</li><li>Oversee product development procedures to identify deviations from quality standards</li><li>Product stability study coordination</li><li>Supervise direct reports, providing guidance and feedback</li><li>Execute and manage processes to ensure effective documentation control</li><li>Recall and mock recall coordination</li></ul><p>PREFERRED QUALIFICATIONS:</p><ul><li>Bachelor’s degree in chemistry, biology, or related field with seven years of professional experience in the pharmaceutical, dietary supplement, or food industry, preferably with five years in a Quality role</li><li>Supervisory or management experience</li><li>ASQ certified CMQ/OE, CQE, CQA, or CFSQA</li><li>Proficient skills in, G Suite, Video Conferencing, Excel, and Word</li><li>Strong organizational skills and the ability to work effectively with a team</li></ul><p>Job Type: Full-time</p><p>Pay: $75,000.00 - $85,000.00 per year</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></ul><p>Supplemental Pay:</p><ul><li>Bonus pay</li></ul><p>COVID-19 considerations:<br />GVB has measures and regulations in place to ensure the health and wellbeing of our employees. We have established social distancing and mask requirements and have been following all state and local regulations.</p><p>Application Question(s):</p><ul><li>Please list any relevant certifications as required by the Job Description.</li><li>Our facility is located in Grass Valley, OR. Are you willing and or able to commute/relocate to Grass Valley?</li></ul><p>Education:</p><ul><li>Bachelor's (Preferred)</li></ul><p>Experience:</p><ul><li>Quality Assurance: 5 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":"GVB Biopharma","logoUrl":"/logos/gvb-biopharma-ec55e466c36a12bccf78758e67009397.jpeg"},"location":{"country":"United States","address":"Portland, OR","city":"Portland","stateProvince":"OR"},"frontendLink":"/job-posting/gvb-biopharma/quality-assurance-manager/902d570c19e691bea0be0768be8453d0","title":"Quality Assurance Manager","hash":"902d570c19e691bea0be0768be8453d0","postingUrl":"https://www.indeed.com/job/quality-assurance-manager-7d19c6939f3de350"},{"employmentType":"Full-time","postedOn":"25 days ago","description":"<div><p>GVB Biopharma is an industry-leading, vertically integrated global leader in the ever-growing hemp industry. We prioritize cannabinoid research, industry innovation, and traceable quality control. GVB operates two state-of-the-art facilities: a 30,000-square-foot food-grade hemp processing facility in Central Oregon and a 40,000-square-foot white-label consumer product manufacturing facility in Las Vegas.</p><p>JOB SUMMARY:<br />This position requires the ability to lead and train Quality professionals in the<br />appropriate application of standards including ISO 9001:2015 and cGMP and support both internal and external customers.</p><p>ESSENTIAL DUTIES AND RESPONSIBILITIES.</p><p>*Other assignments, projects, and duties may be required:</p><p>Primary responsibilities include:</p><ul><li>Leads in the development of a climate of quality and safety, seeking continuous</li></ul><p>improvement, providing sound vision and guidance in the application of Quality standards</p><ul><li>Administrate and manage the Quality Management System, driving to completion events such as corrective actions, change control, deviations, nonconforming product, and audit reports</li><li>Aid in determining root cause for nonconforming events and evaluate corrective and preventive actions for lifecycle effectiveness</li><li>Author or approve key Quality System documents</li><li>Author, approve and defend as applicable corrective actions</li><li>Effectiveness monitoring of site Quality Systems, presenting during the management review cycle</li><li>Assist and support Audit Program to evaluate compliance requirements and identify areas requiring corrective action or opportunities for improvement</li><li>Assure timely completion of corrective and preventive actions</li><li>Maintain and support procedures to ensure the compliance of all products and packaging</li><li>Support supplier approval program, setting requirements for raw material and component products and tracking supplier compliance</li><li>Oversee product development procedures to identify deviations from quality standards</li><li>Product stability study coordination</li><li>Supervise direct reports, providing guidance and feedback</li><li>Execute and manage processes to ensure effective documentation control</li><li>Recall and mock recall coordination</li></ul><p>PREFERRED QUALIFICATIONS:</p><ul><li>Bachelor’s degree in chemistry, biology, or related field with seven years of professional experience in the pharmaceutical, dietary supplement, or food industry, preferably with five years in a Quality role</li><li>Supervisory or management experience</li><li>ASQ certified CMQ/OE, CQE, CQA, or CFSQA</li><li>Proficient skills in, G Suite, Video Conferencing, Excel, and Word</li><li>Strong organizational skills and the ability to work effectively with a team</li></ul><p>Job Type: Full-time</p><p>Pay: $75,000.00 - $85,000.00 per year</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></ul><p>Supplemental Pay:</p><ul><li>Bonus pay</li></ul><p>COVID-19 considerations:<br />GVB has measures and regulations in place to ensure the health and wellbeing of our employees. We have established social distancing and mask requirements and have been following all state and local regulations.</p><p>Application Question(s):</p><ul><li>Please list any relevant certifications as required by the Job Description.</li><li>Our facility is located in Grass Valley, OR. Are you willing and or able to commute/relocate to Grass Valley?</li></ul><p>Education:</p><ul><li>Bachelor's (Preferred)</li></ul><p>Experience:</p><ul><li>Quality Assurance: 5 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":"GVB Biopharma","logoUrl":"/logos/gvb-biopharma-ec55e466c36a12bccf78758e67009397.jpeg"},"location":{"country":"United States","address":"Grass Valley, OR 97029","city":"Grass Valley","stateProvince":"OR"},"frontendLink":"/job-posting/gvb-biopharma/quality-assurance-manager/507e9b83c367c13076c8f60a2cee62db","title":"Quality Assurance Manager","hash":"507e9b83c367c13076c8f60a2cee62db","postingUrl":"https://www.indeed.com/job/quality-assurance-manager-6a79804237493892"},{"employmentType":"Full-time","postedOn":"25 days ago","description":"<div><p>GVB Biopharma is an industry-leading, vertically integrated global leader in the ever-growing hemp industry. We prioritize cannabinoid research, industry innovation, and traceable quality control. GVB operates two state-of-the-art facilities: a 30,000-square-foot food-grade hemp processing facility in Central Oregon and a 40,000-square-foot white-label consumer product manufacturing facility in Las Vegas.</p><p>JOB SUMMARY:<br />This position requires the ability to lead and train Quality professionals in the<br />appropriate application of standards including ISO 9001:2015 and cGMP and support both internal and external customers.</p><p>ESSENTIAL DUTIES AND RESPONSIBILITIES.</p><p>*Other assignments, projects, and duties may be required:</p><p>Primary responsibilities include:</p><ul><li>Leads in the development of a climate of quality and safety, seeking continuous</li></ul><p>improvement, providing sound vision and guidance in the application of Quality standards</p><ul><li>Administrate and manage the Quality Management System, driving to completion events such as corrective actions, change control, deviations, nonconforming product, and audit reports</li><li>Aid in determining root cause for nonconforming events and evaluate corrective and preventive actions for lifecycle effectiveness</li><li>Author or approve key Quality System documents</li><li>Author, approve and defend as applicable corrective actions</li><li>Effectiveness monitoring of site Quality Systems, presenting during the management review cycle</li><li>Assist and support Audit Program to evaluate compliance requirements and identify areas requiring corrective action or opportunities for improvement</li><li>Assure timely completion of corrective and preventive actions</li><li>Maintain and support procedures to ensure the compliance of all products and packaging</li><li>Support supplier approval program, setting requirements for raw material and component products and tracking supplier compliance</li><li>Oversee product development procedures to identify deviations from quality standards</li><li>Product stability study coordination</li><li>Supervise direct reports, providing guidance and feedback</li><li>Execute and manage processes to ensure effective documentation control</li><li>Recall and mock recall coordination</li></ul><p>PREFERRED QUALIFICATIONS:</p><ul><li>Bachelor’s degree in chemistry, biology, or related field with seven years of professional experience in the pharmaceutical, dietary supplement, or food industry, preferably with five years in a Quality role</li><li>Supervisory or management experience</li><li>ASQ certified CMQ/OE, CQE, CQA, or CFSQA</li><li>Proficient skills in, G Suite, Video Conferencing, Excel, and Word</li><li>Strong organizational skills and the ability to work effectively with a team</li></ul><p>Job Type: Full-time</p><p>Pay: $75,000.00 - $85,000.00 per year</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></ul><p>Supplemental Pay:</p><ul><li>Bonus pay</li></ul><p>COVID-19 considerations:<br />GVB has measures and regulations in place to ensure the health and wellbeing of our employees. We have established social distancing and mask requirements and have been following all state and local regulations.</p><p>Application Question(s):</p><ul><li>Please list any relevant certifications as required by the Job Description.</li><li>Our facility is located in Grass Valley, OR. Are you willing and or able to commute/relocate to Grass Valley?</li></ul><p>Education:</p><ul><li>Bachelor's (Preferred)</li></ul><p>Experience:</p><ul><li>Quality Assurance: 5 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":"GVB Biopharma","logoUrl":"/logos/gvb-biopharma-ec55e466c36a12bccf78758e67009397.jpeg"},"location":{"country":"United States","address":"Biggs Junction, OR","city":"Biggs Junction","stateProvince":"OR"},"frontendLink":"/job-posting/gvb-biopharma/quality-assurance-manager/b5f270262555106e090e4bb7a1b2370d","title":"Quality Assurance Manager","hash":"b5f270262555106e090e4bb7a1b2370d","postingUrl":"https://www.indeed.com/job/quality-assurance-manager-e7c08ce075bd29d2"},{"employmentType":"Full-time","postedOn":"5 days ago","description":"<div><p>We are currently seeking candidates for the position of Quality Assurance Manager - Product Compliance.</p><p>Reporting to the Director of Quality Assurance, the ideal candidate will be a motivated individual with ability to lead a fast-paced team with a sense of urgency. This successful candidate will show strong attention to detail, have excellent organizational skills, and maintain a positive and professional attitude in a fast paced and changing work environment. Our incumbent will manage a team of Compliance individuals to coordinate the review of records and assure product compliance for finished goods and intermediate stages. Being a team player is a definite key for the role of Quality Assurance Manager- Product Compliance as they will work closely with many departments and individuals including Planning, Production, Shipping, Inventory, Operational Excellence, and Regulatory.</p><p><b>Key Responsibilities:</b></p><p>• Carry out management responsibilities in accordance with our best practices policies, procedures, applicable acts, and regulations;</p><p>• Provide coaching, training, and support to employees;</p><p>• Manage a team of QA Controllers, Coordinators and Administration in the execution of duties assigned to the Compliance team, providing training, guidance, and support to the team;</p><p>• Manages adherence to Organigram's product quality and regulatory compliance programs ensuring that the products produced comply with the Cannabis Act, pertinent regulations, and individual customer requirements;</p><p>• Ensures that product flow timelines are met; organization for testing of every lot, analyzing results, assigning appropriate disposition and thorough communication;</p><p>• Acts as a primary product compliance liaison with Health Canada;</p><p>• Approve product quality standards, manage product specifications and customer CoA's;</p><p>• Manage non-conforming product by analyzing root causes and developing corrective actions;</p><p>• Monitor test result data trends; identify and facilitate changes to achieve specifications and targets;</p><p>• Assists with traceability exercises at minimum of twice per year, drives continuous improvement from resulting CAPA's;</p><p>• Manages the Stability Program through organization, coordination and reporting of results;</p><p>• Assist with ongoing development and maintenance of the Quality Management System;</p><p>• Perform internal facility inspections and audits;</p><p>• Provide quality guidance for new product development, product changes, packaging changes, new equipment, and facility design;</p><p>• Product compliance budgeting and invoice review;</p><p>• Other duties as may be assigned.</p><p><b>Qualifications:</b></p><p>• Post-secondary education or equivalent experience in a regulated environment, food manufacturing and/or in a pharmaceutical manufacturing environment;</p><p>• 2-3 years experience in a leadership role;</p><p>• Previous experience in Quality Assurance and development of QMS;</p><p>• Proficient in Word, PowerPoint, Outlook, Excel, inventory management systems;</p><p>• Proven leadership experience and teamwork;</p><p>• Excels in critical thinking for problem solving, and decision-making skills;</p><p>• Displays strong attention to detail;</p><p>• Has a well-established sense of urgency;</p><p>• Strong communication (written and verbal) skills.</p><p>For more information and to apply online, please visit the Careers page of our Website at: https://www.organigram.ca/careers</p><p>While we thank all candidates for their interest, only those selected will be contacted.</p><p>Organigram is an equal opportunity employer</p></div>","company":{"website":"organigram.ca","companyType":"Public/Established","name":"OrganiGram","logoUrl":"/logos/organigram-inc-5d1310a944f393e0ae6a0a47db2f9dfb.png"},"location":{"country":"Canada","address":"Moncton, NB","city":"Moncton","stateProvince":"NB"},"frontendLink":"/job-posting/organigram/quality-assurance-manager-product-compliance-organigram-inc-in/b1a3798bba2b26a43a86278a748e5732","title":"Quality Assurance Manager Product Compliance Organigram Inc In...","hash":"b1a3798bba2b26a43a86278a748e5732","postingUrl":"https://ca.mncjobz.com/jobs/quality-assurance-manager-product-compliance-organigram-inc-in-moncton-nb-yesterday-new-moncton-1187749"},{"employmentType":"Full-time","postedOn":"25 days ago","description":"<div><p>Who We AreCannTrust is an award-winning, federally regulated licensed cannabis producer, with locations in Vaughan and Niagara, Ontario. We are proudly Canadian, operating a portfolio of well-known brands including CannTrust, estora Liiv and Synr.g. At CannTrust, we are committed to providing exceptional customer experience, quality products and consistent, standardized dosing. Our greenhouses produce 95% grade A cannabis flower, which is sold in dried flower, oil and vegan capsule formats. Founded in 2014, our continued success in the medical cannabis market and subsequent expansion into the recreational business, led to us being named Licensed Producer of the Year at the Canadian Cannabis Awards 2018.Join us in our mission to support our customers and empower our patients to improve their quality of life, by enriching the cannabis experience with the best quality products, educational resources and outstanding service.Who You AreThe ideal candidate is an agile, business savvy individual who is committed to getting better everyday. You are a passionate influencer with strong communication skills, who is open to giving and receiving feedback. You are customer-centric with an ability to act as a mentor amongst your peers. Of course, you also deliver consistent results by aligning yourself with CannTrust values.Job Summary The Manager, Quality Assurance- Production under the leadership and guidance of the Senior Director, Quality Assurance, is responsible for quality and compliance support at the production (shop floor) level within the manufacturing, packaging, and warehousing of Cannabis products. Key Responsibilities · Perform Quality Assurance duties and responsibilities as assigned by Senior Director, Quality Assurance and QAP · Assists Senior Director, Quality Assurance and QAP with day-to-day Quality Assurance activities to drive continuous improvement and efficiencies · Assists Senior Director, Quality Assurance and QAP in the investigations and closing of deviations, CAPAs and Change Controls in accordance with GPP and regulatory requirements · Minimize risks and maintain standards of quality and GPP compliance at the production level. · Mentoring within and outside of the department, staff development, monitoring performance of the quality within the department· Manage a team of highly productive QA-Production specialists, all manufacturing shifts and flexible to cover different shifts as required by business need· Structure and organize QA- Production activities to ensure i) alignment of QA- Production resources with the shop floor platforms; ii) coaching within the QA-Production department to drive consistency in approach, manage risks, and maintain the required standard of quality and GPP compliance, iii) daily real time batch record review performed minimizing errors upon final review, iv) coverage for non-routine shifts, v) inspections, sampling ( raw materials, components, cannabis and labels), line clearance, sanitation verification, in process testing, and label control are performed according to CannTrust proceduresEstablishing and maintaining a well-motivated and enthusiastic team with a good working environment· Ensure shop floor investigations are comprehensive, enable determination of root cause, corrective / preventive actions, product impact, and meet closure time requirements both for the investigation and timely lot release· Review and approval of QA-Production and other assigned GPP SOPs and change controls assessments· Collaborate with the shop floor platforms to provide coaching and knowledge transfer to strengthen quality culture and GPP understanding · Setting internal standards for KPIs · Regular meeting of quality department, oversight of major initiatives, maintaining deadlines and accountability · Maintaining in-process Quality coverage · Report on key quality metrics on a weekly, monthly basis and as deemed necessary by Senior Director, Quality Assurance and report and trend reports to identify and mitigate negative trends for actionSupport consistent and appropriate quality decision making on the shop floor to mitigate deviation generation rateSupport inspection/audit readiness at all times and contribute to follow up correspondenceOversight of QA-Production Sage transactions and final disposition of secondary components and product labels.Support execution of continuous improvement activities to meet strategic goals to improve efficiencies and productivity as outlined in yearly objectives. People Leader Job RequirementsHolds others and self-accountable to gaps in performance, is a champion of feedbackActs with Integrity: Demonstrates responsible, ethical, and honest behavior while consistently leading by example; models the CannTrust valuesMotivates team to take timely action, resolves customer escalations in a timely mannerMonitors progress to departmental goals with company strategySets department goals &amp; objectives and supports direct reports with achieving results and development plansEncourages team to be involved in decisions, encourages talent developmentExecutes the performance management cycle activities for the teamStrong communication skills, ability to promote learning and development; can have difficult conversationsComplies with all company policies Education &amp; Experience· B.Sc. in Chemistry, Biochemistry, Biology, Pharmaceutical Sciences, Engineering (or related field).· Minimum 4-6 years’ experience in quality assurance or related area preferably within the Cannabis, pharmaceutical or food industry and minimum of 3-year management experience.· Experience in manufacturing operations and controls, quality systems, document control, batch disposition, regulations, validation, leadership, influencing, and negotiation.· Experience in Quality Systems: Change Control, Deviation, CAPA, Document Control and complaints · Strong quality decision making skills; with an understanding of root cause analysis and ability to lead and support critical investigations · Understanding of equipment, manufacturing processes, maintenance, and quality standards.· Demonstrated and thorough knowledge of GPP relative to Health Canada and other related global regulations.· Knowledge of HACCP or other quality systems.Requirements Excellent written and oral communication skills, fluent in EnglishProficiency in Microsoft Outlook, Word, Excel, PowerPoint Strong problem solving and decision-making skills / tools to resolve issues in a manner that is customer focused; but without compromise to making good quality decisionsAvailable to travel to other company locationsMust pass an RCMP security clearanceDemonstrated strategic, process-driven, analytical, and critical thinking.Strong multitasking, ability to prioritize key workStrong management skills, ability to collaborate, take initiative, and lead othersMotivated &amp; driven individual Physical DemandsWhile performing the responsibilities of the job, the employee is required to lift up to and including 25lbs, sit and/or stand for extended periods of time and reach with arms/hands. Walking, climbing stairs, standing, and moving items is occasionally required. The employee must wear the required PPE to complete their job functions. The company reserves the right to modify PPE requirements based on regulatory, compliance and operational needs.Work EnvironmentWhen employees are required to perform duties within the Manufacturing facilities, they may be exposed to unprocessed cannabis products/supplies. The Manufacturing environment can be temperate, noisy and dusty at times. The employee will be provided with the appropriate (PPE) Personal Protective Equipment, and they must adhere to legal requirements regarding PPE to manage their own personal safety under these conditions. In addition, to ensure compliance and minimize contamination within a controlled environment, the employees may be required to wear latex gloves and cleanroom suit</p></div>","company":{"website":"canntrust.com","companyType":"Public/Established","name":"CannTrust","logoUrl":"/logos/canntrust-d201bb4ca139eb0b36f0ce0af7b71eca.png"},"location":{"country":"Canada","address":"Regional Municipality of York, ON","city":"Regional Municipality Of York","stateProvince":"ON"},"frontendLink":"/job-posting/canntrust/manager-quality-assurance-production/4030047fae6e39be169e5558ff90191b","title":"Manager, Quality Assurance- Production","hash":"4030047fae6e39be169e5558ff90191b","postingUrl":"https://ca.trabajo.org/job-166-20210827-d9603245f1be957448772c6df4fce94b"},{"employmentType":"Full-time","postedOn":"8 days ago","description":"<div><p>Kiva Confections ) is the premier cannabis-infused edibles company in California, the largest cannabis market in the world. Kiva's line includes Kiva Chocolate Bars, Terra Bites, Petra Mints, and Camino Gummies. Our products are crafted from premium ingredients and skillfully combined with California cannabis.</p><p>Since our beginning in 2010, our goal is to create confections that redefine what a cannabis confection ought to be.</p><p>By applying art and science to ensure a deliciously consistent experience every time, we continue to deliver on that mission today.</p><p>We have aggressive growth plans as the legal market, and consumer adoption continues to expand. Key growth initiatives include bold platform innovation, best in class marketing, geographic expansion, strategic partnerships, and more.</p><p>We are resourced for this explosive growth and looking for great people to help take us to the next level.</p><p><b>Job Summary</b></p><p>The Geo FSQA Manager is a vital partner in the daily success of Kiva Confections.</p><p>This role ensures that out of state co-manufacturers comply with all Kiva standards for Food Safety and both product Quality and Compliance, overseeing audits to an established and accepted Food Industry standard.</p><p>This individual oversees quality systems and facilities in partner states, current and future, and will be the liaison between FSQA in California and Quality teams in all other out of state co-manufacturers.</p><p>In collaboration with the Director of FSQA, Sr.</p><p>FSQA Manager and Geo team, the Geo FSQA Manager drives geo partner manufacturing plants to GFSI level audit compliance through training and audits.</p><p>The Geo FSQA Manager will be responsible for making KIVA's core Quality and Food Safety systems applicable to Geo States and implementing the quality management systems in all co-manufacturing facilities in partner states.</p><p>This job is for you if</p><p>• You have extensive knowledge and experience in leading a Food Safety and Quality Assurance program in a food manufacturing plant</p><p>• You understand the importance of versatility and flexibility of Quality without compromising Food Safety.</p><p>• You are a wealth of compliance knowledge, with the ability for coaching and mentoring those around you</p><p>• You love building teams and thrive in a fast-paced, high-growth environment</p><p>• You are a great coach and mentor, teaching with compassion and empathy, but leading with accountability</p><p>• You are results-driven</p><p>• You have experience in GFSI facility audit and inspections</p><p>As the Geo Food Safety Quality Assurance Manager, you'll.</p><p>• Partner with all out of state Kiva GEO Food Safety and Quality program managers to assure compliance and Continuous Improvements.</p><p>• Develop and manage Document Control for partner states.</p><p>• Champion Food Safety and Quality programs and ensure compliance in partner states such as: internal audit, supplier approval, chemical control programs, amongst others, and ensure compliance to all related policies, procedures, and specifications.</p><p>• Schedule, plan, and perform frequent system, site, data audits for all partner state co-manufacturers alongside the Director and Sr. Manager of FSQA. Follow up on any unresolved audit findings.</p><p>• Assure that issues from audits are promptly communicated to the appropriate team members, assist with the development of a corrective action plan and facilitate resolution of all audit findings</p><p>• Proactively identify potential and emerging food safety issues and develop mitigation strategies alongside the Director and Sr. Manager of FSQA.</p><p>• Collaborating with co-manufacturer program managers to provide continuous and rigorous assessment of their Quality Management System including CAPA, internal audits, non conformances, and other processes as necessary to identify and implement improvements.</p><p>• Be a subject matter expert on Internal Audit and CAPA practices.</p><p>• Review all partner states' packaging artwork for compliance and product safety claims.</p><p>• Travel to out of state co-manufacturer facilities</p><p>What we're looking for</p><p>• Bachelor's Degree in Food Science, Science or a related field is required</p><p>• 3-5 years of experience as a FSQA Manager in a food manufacturing facility with experience building and leading teams and building programs in both remote and in-person capacities</p><p>• Cannabis experience is highly preferred, but not mandatory.</p><p>• Salesforce experience is a plus</p><p>• Relevant certifications, training and/or experience: GFSI audit scheme, PCQI, HACCP, etc. are a plus.</p><p>• Ability to prioritize and manage time efficiently</p><p>• Organized and able to handle multiple projects and meet deadlines</p><p>• Self-directed and able to work autonomously</p><p>• Excellent people skills, including listening skills. Team-oriented attitude.</p><p>• Strong verbal and written communication skills.</p><p>Kiva Confections 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>DISCLOSURE TO JOB APPLICANTS PURSUANT TO THE CALIFORNIA CONSUMER PRIVACY ACT (CCPA)</p><p><b>As part of your job application and the Company's evaluation of your candidacy, the Company collects, receives, maintains, and uses the following types of Personal Information about you for the business purposes identified for each category:</b></p><p><b>Category:</b></p><p>Personal Identifiers</p><p><b>Examples:</b></p><p>Name, alias, postal or mailing address, email address, telephone number, social security number, driver's license or state identification card number, passport number</p><p><b>Business Purpose:</b></p><p>• To comply with state and federal law and regulations requiring; employers to maintain certain records;</p><p>• To evaluate your job application and candidacy for employment;</p><p>• To obtain and verify background check and references; and</p><p>• To communicate with you regarding your candidacy for employment.</p><p><b>Category:</b></p><p>Pre-Hire Information</p><p><b>Examples:</b></p><p>Job application, resume, background check results, job interview notes, and candidate evaluation records</p><p><b>Business Purpose:</b></p><p>Same as above</p><p><b>Category:</b></p><p>Employment History</p><p><b>Examples:</b></p><p>Information regarding prior job experience, positions held, names of prior supervisors, reference information, skills and when permitted by applicable law your salary history or expectations</p><p><b>Business Purpose:</b></p><p>Same as above</p><p><b>Category:</b></p><p>Education Information</p><p><b>Examples:</b></p><p>Information from resumes regarding educational history; transcripts or records of degrees, vocational certifications, licenses obtained</p><p><b>Business Purpose:</b></p><p>Same as above</p><p>If you become employed by the Company, the Company will notify you of additional categories of Personal Information that it collects, receives, and maintains for business purposes</p></div>","company":{"companyType":"Private/Established","name":"Kiva Confections","logoUrl":"/logos/kiva-confections-504a60c51f66386caf47736579c8f2e6.jpeg"},"location":{"country":"United States","address":"Oakland, CA, USA","city":"Oakland","stateProvince":"CA"},"frontendLink":"/job-posting/kiva-confections/food-safety-quality-assurance-manager-geo-external-partners/54bd3b44cd12da04686f7391e20cdb4a","title":"Food Safety Quality Assurance Manager - Geo External Partners","hash":"54bd3b44cd12da04686f7391e20cdb4a","postingUrl":"https://us.bebee.com/job/20210914-345e3db4d29ae0ee131acdf186093291"},{"postedOn":"19 days ago","description":"<div><div></div><div><div><p><b>Quality Assurance Manager</b><br /><b>Administrative Officer R24</b><br /></p><p>At the Liquor Distribution Branch (LDB) our vision of ‘Service. Relationships. Results.’ is all about providing a valued service, building strong relationships with our stakeholders, and achieving greater results for the province.</p><p>The LDB is one of two branches of government responsible for the cannabis and liquor industry of B.C. We operate the wholesale distribution of beverage alcohol and non-medical cannabis within the province, as well as the household retail brands of BC Liquor Stores and BC Cannabis Stores.</p><p>We employ nearly 5,000 people in over 200 communities and have hundreds of career opportunities spanning our entire wholesale, retail and corporate operations – from supply chain logistics, to high-tech solutions, and everything in between. The LDB has been named one of BC’s Top Employers 12 times over for offering exceptional places to work, flexible work hours and earned days off, extended health and dental benefits, maternity and parental leave top-up payments, a pension program, in-house professional and leadership development, and subsidies for professional accreditation.</p><p>The LDB Wholesale Operations team is responsible for the registration, procurement, customs clearance, selling and distribution of liquor products for the province of British Columbia. Our stakeholders comprise approximately 800 suppliers, over 1500 retail outlets and 8000 licensed establishments. Working in collaboration with our suppliers and agents, our vision is to provide a reliable and efficient service to support the success of our customers. There are five key divisions within the business; Supply Chain, Pricing, Imports, Customer Service and Distribution. Each of our teams work closely in alignment with each other to provide a seamless customer experience and deliver on our service goals.</p><p>The Quality Assurance (QA) Manager is responsible for all activities related to the evaluations performed on operational policy and procedures through call monitoring, including reviewing and auditing customer interactions (email, telephone, etc.) along with reviewing and investigating customer survey responses for the Wholesale Customer Centre (WCC).</p><p>The QA Manager is responsible for facilitating calibration/group sessions regarding the quality program and identifying areas of service improvements and developing programs that improve the overall quality of the customer’s experience when interacting with the WCC. The QA Manager is responsible for providing feedback to operational teams on the results of the call evaluations, present objective recommendations/suggestions for improvement and identifies potential risks and gaps.</p><p>The QA Manager requires the ability to work in a constructive, non-biased and collaborative manner by establishing positive working relationships, partnering with the WCC leadership, team members and other resources. This position requires the ability to gain the confidence and trust of others by demonstrating professionalism and expertise in an ever changing environment.</p><p>Candidates may be required to work a variety of shift patterns. A criminal record check is required.</p><p>For complete details about this opportunity, including accountabilities, please refer to the attached job description, also located in the Additional Information section at the bottom of the posting.</p><p>An eligibility list for permanent or temporary future opportunities may be established.</p><p><b>Position Requirements:</b></p><p><b>Education and Experience:</b></p><ul><li>Minimum of three (3) years recent (within the last five years), related experience in a customer service operation as an analyst or manager, in a role focused on quality assurance and customer experience.</li><li>Post-secondary education or related coursework including formal quality assurance training and dispute resolution training.</li><li>Experience with coaching and development for performance improvement,</li><li>Experience leading a team.</li></ul><p>An equivalent combination of experience, training, and education may be considered. i.e., five (5) years of recent, related experience as stated above may be considered equivalent to the educational requirement.</p><p><b>How to Apply &amp; Application Requirements:</b></p><p>In order to be considered for this position, your application must clearly demonstrate how you meet the education and experience as outlined in the Position Requirements section above. Applicants selected to move forward in the hiring process may be assessed on the knowledge, skills, abilities and competencies as outlined in the attached Job Description.</p><p>A cover letter is required as part of your application. The content and/or format of your cover letter may be evaluated as part of the assessment process.</p><p>Ensure your resume includes your educational accomplishments, employment history including start and end dates (month and year) of your employment, and any relevant information that relates to the job to which you are applying.</p><p>For specific position-related enquiries, please contact at <b>Rebecca Levick, A/HR Advisor at <span><a href=\"tel:+1-604-252-5053\">604-252-5053</a></span></b>.</p><p>Only applications submitted using the BC Public Service Recruitment System on this website will be accepted. For more information about how to create or update your profile, please refer to the attached Application Instructions or refer to the Job Application page on the MyHR website. If you are experiencing technical difficulty applying for a competition, please send an e-mail to [email protected] before the stated closing time, and they will respond as soon as possible to assist you.</p><p><b>NOTE: </b>Applications will be accepted until 11:00pm Pacific Time on the closing date of the competition.</p></div></div></div>","company":{"companyType":"Government","name":"BC Public Service","logoUrl":"/logos/bc-public-service-e5abe612080c1bade033d7a9bffff9fa.jpeg"},"location":{"country":"Canada","address":"Burnaby, BC","city":"Burnaby","stateProvince":"BC"},"frontendLink":"/job-posting/bc-public-service/admn-o-24r-quality-assurance-manager/52dbbdf75f62c733a1332e8f1ebd1d94","title":"ADMN O 24R - Quality Assurance Manager","hash":"52dbbdf75f62c733a1332e8f1ebd1d94","postingUrl":"https://ca.indeed.com/job/admn-o-24r-quality-assurance-manager-bf6260df61d128e3"},{"employmentType":"Full-time","postedOn":"5 days ago","description":"<div><p><b>Who We Are</b></p><p>Lifeist_ is a new, bold, and disruptive type of wellness company, striving to connect the world with safe, innovative and often daring pathways to individual definitions of wellness.</p><p>Health &amp; wellness is evolving and becoming increasingly complicated. Lifeist is a global health platform striving to connect the world with safe, innovative and daring pathways to their individual definition of wellness. Whether humans need to find a product that makes them feel relaxed, energetic, productive, or internally healthier, Lifeist will connect them with these innovative solutions and if they don't exist, create them.</p><p>Lifeist’s portfolio of businesses include: CannMart.com which provides Canadian customers with a diverse selection of cannabis products and accessories, and its U.S. customers with hemp-derived CBD and smoking accessories; CannMart’s Canadian recreational cannabis distribution business facilitating sales to a number of provincial government control boards; and CannMart Labs Inc., a state-of-the-art BHO extraction facility set to produce higher margin cannabis concentrate products.</p><p>Our Positioning - Higher Living</p><p>Our Mission - To Let The Normal Human Unlock Extraordinary</p><p>Our Vision - To Simplify Your Path To Wellness</p><p><b>Who You Are</b></p><p>The QA/RA Manager will be a key member of CannMart Inc’s. Quality and Regulatory team. The ideal candidate will be quality driven, with a natural ability to problem solve. CannMart is looking for someone who is an excellent communicator, and has a natural ability to work with a variety of people, as well as be a team leader.</p><p><b>Responsibilities</b></p><p>• Ensure compliance with applicable regulatory frameworks (e.g. as prescribed by the Cannabis Act and Cannabis Regulations).</p><p>• Determine internal best practices and champion a quality culture of excellence.</p><p>• Manage the organizational security plan, security clearance applications, changes to key personnel and other communications with the regulator pertaining to physical security and security cleared personnel as well as new licence applications, licence amendments and renewal applications.</p><p>• Manage activities performed through the Cannabis Tracking and Licensing System.</p><p>• Lead a growing quality and regulatory team through effective relationship management, performance management, training and coaching.</p><p>• Ensure that licensed activities are conducted according to standard operating procedures and work instructions and that controlled documents are kept up to date.</p><p>• Effective deviation management, including root cause analysis and investigation, corrective action and implementation of quality event reporting.</p><p>• Identify key performance indicators that will drive continuous improvement and compliance.</p><p>• Train team members on Good Production Practices, Good Documentation Practices, Good Recordkeeping Practices and other quality systems, as required.</p><p>• Collaborate with other business leaders as a quality and regulatory stakeholder to ensure operational success.</p><p>• Manage vendor qualification and supplier audit activities.</p><p>• Continuously improve the electronic quality management system and quality systems processes.</p><p>• Represent CannMart during audits and in communications with regulatory authorities and external business partners.</p><p>• Support validation and qualification activities, coordinate analytical testing using validated methods and establish a preventive control program.</p><p>• Coordinate quality investigations, complaint handling and mock recall activities.</p><p>• Additional duties as required from time-to-time</p><p>Education &amp; Experience</p><p>• Bachelor’s degree in the sciences or a combination of relevant education and experience.</p><p>• Three or more years of experience in the cannabis industry is preferred.</p><p>• Prior experience in vendor management is required.</p><p>• Prior experience in a compliance function is required.</p><p>• Prior experience in quality investigations is required.</p><p>• Prior experience in food safety is an asset.</p><p>• Prior experience establishing quality control programs is an asset.</p><p>• Prior experience leading validation and qualification is an asset.</p><p>• Security clearance or QAP standing with Health Canada is an asset.</p><p>• Effective communication skills are required.</p><p>• Demonstrated proficiency in problem solving and risk-based decision making.</p><p>• Demonstrated leadership skills.</p><p>• Demonstrated investigation and auditing proficiency.</p><p>• Demonstrated ability to interpret regulatory requirements.</p><p>• Demonstrated ability to collaborate with multiple internal and external stakeholders.</p><p>• Demonstrated ability to continuously improve quality systems and champion a quality culture.</p><p>Personal Traits We Love to See</p><p>• You show intellectual curiosity</p><p>• You demand integrity</p><p>• You practise gratitude</p><p>• You make meaningful connections</p><p>• You are innovative</p><p>This role will be remote, within Ontario, with the ability to attend on-site support to audit and compliance activities as needed (Facility is located in Etobicoke). We thank you for your interest in employment opportunities at Lifeist_. Please note, only the candidates who are selected for an interview will be contacted.Lifeist_ welcomes and encourages applications from people with disabilities. Accommodations are available on request for candidates taking part in all aspects of the selection process.</p><p>Powered by JazzHR</p></div>","company":{"website":"lifeist.com","companyType":"Public/Established","name":"Namaste Technologies","logoUrl":"/logos/namaste-technologies-9eb6b7a0098e7ad0a52503074f6bbbbd.png"},"location":{"country":"Canada","address":"Caledonia, ON","city":"Caledonia","stateProvince":"ON"},"frontendLink":"/job-posting/namaste-technologies/qa-ra-manager/1609755a38789a988927f36980a36070","title":"QA/RA Manager","hash":"1609755a38789a988927f36980a36070","postingUrl":"https://ca.linkedin.com/jobs/view/qa-ra-manager-at-namaste-technologies-2723081843"},{"employmentType":"Full-time","postedOn":"6 days ago","description":"<div><p><b>Who We Are</b></p><p>Lifeist_ is a new, bold, and disruptive type of wellness company, striving to connect the world with safe, innovative and often daring pathways to individual definitions of wellness.</p><p>Health &amp; wellness is evolving and becoming increasingly complicated. Lifeist is a global health platform striving to connect the world with safe, innovative and daring pathways to their individual definition of wellness. Whether humans need to find a product that makes them feel relaxed, energetic, productive, or internally healthier, Lifeist will connect them with these innovative solutions and if they don't exist, create them.</p><p>Lifeist's portfolio of businesses include: which provides Canadian customers with a diverse selection of cannabis products and accessories, and its U.S. customers with hemp-derived CBD and smoking accessories; CannMart's Canadian recreational cannabis distribution business facilitating sales to a number of provincial government control boards; and CannMart Labs Inc a state-of-the-art BHO extraction facility set to produce higher margin cannabis concentrate products.</p><p>Our Positioning - Higher Living</p><p>Our Mission - To Let The Normal Human Unlock Extraordinary</p><p>Our Vision - To Simplify Your Path To Wellness</p><p><b>Who You Are</b></p><p>The QA/RA Manager will be a key member of CannMart Inc's. Quality and Regulatory team. The ideal candidate will be quality driven, with a natural ability to problem solve. CannMart is looking for someone who is an excellent communicator, and has a natural ability to work with a variety of people, as well as be a team leader.</p><p><b>Responsibilities</b></p><p>• ​​ Ensure compliance with applicable regulatory frameworks (e.g. as prescribed by the Cannabis Act and Cannabis Regulations ).</p><p>• Determine internal best practices and champion a quality culture of excellence.</p><p>• Manage the organizational security plan, security clearance applications, changes to key personnel and other communications with the regulator pertaining to physical security and security cleared personnel as well as new licence applications, licence amendments and renewal applications.</p><p>• Manage activities performed through the Cannabis Tracking and Licensing System.</p><p>• Lead a growing quality and regulatory team through effective relationship management, performance management, training and coaching.</p><p>• Ensure that licensed activities are conducted according to standard operating procedures and work instructions and that controlled documents are kept up to date.</p><p>• Effective deviation management, including root cause analysis and investigation, corrective action and implementation of quality event reporting.</p><p>• Identify key performance indicators that will drive continuous improvement and compliance.</p><p>• Train team members on Good Production Practices, Good Documentation Practices, Good Recordkeeping Practices and other quality systems, as required.</p><p>• Collaborate with other business leaders as a quality and regulatory stakeholder to ensure operational success.</p><p>• Manage vendor qualification and supplier audit activities.</p><p>• Continuously improve the electronic quality management system and quality systems processes.</p><p>• Represent CannMart during audits and in communications with regulatory authorities and external business partners.</p><p>• Support validation and qualification activities, coordinate analytical testing using validated methods and establish a preventive control program.</p><p>• Coordinate quality investigations, complaint handling and mock recall activities.</p><p>• Additional duties as required from time-to-time</p><p>Education &amp; Experience</p><p>• Bachelor's degree in the sciences or a combination of relevant education and experience.</p><p>• Three or more years of experience in the cannabis industry is preferred.</p><p>• Prior experience in vendor management is required.</p><p>• Prior experience in a compliance function is required.</p><p>• Prior experience in quality investigations is required.</p><p>• Prior experience in food safety is an asset.</p><p>• Prior experience establishing quality control programs is an asset.</p><p>• Prior experience leading validation and qualification is an asset.</p><p>• Security clearance or QAP standing with Health Canada is an asset.</p><p>• Effective communication skills are required.</p><p>• Demonstrated proficiency in problem solving and risk-based decision making.</p><p>• Demonstrated leadership skills.</p><p>• Demonstrated investigation and auditing proficiency.</p><p>• Demonstrated ability to interpret regulatory requirements.</p><p>• Demonstrated ability to collaborate with multiple internal and external stakeholders.</p><p>• Demonstrated ability to continuously improve quality systems and champion a quality culture.</p><p>Personal Traits We Love to See</p><p>• You show intellectual curiosity</p><p>• You demand integrity</p><p>• You practise gratitude</p><p>• You make meaningful connections</p><p>• You are innovative</p><p>This role will be remote, within Ontario, with the ability to attend on-site support to audit and compliance activities as needed ( Facility is located in Etobicoke). We thank you for your interest in employment opportunities at Lifeist_. Please note, only the candidates who are selected for an interview will be contacted.Lifeist_ welcomes and encourages applications from people with disabilities. Accommodations are available on request for candidates taking part in all aspects of the selection process</p></div>","company":{"website":"lifeist.com","companyType":"Public/Established","name":"Namaste Technologies","logoUrl":"/logos/namaste-technologies-9eb6b7a0098e7ad0a52503074f6bbbbd.png"},"location":{"country":"Canada","address":"Canada"},"frontendLink":"/job-posting/namaste-technologies/qa-ra-manager/afd7d518386247a7bff0c5bef7e2f8dd","title":"QA/RA Manager","hash":"afd7d518386247a7bff0c5bef7e2f8dd","postingUrl":"https://ca.bebee.com/job/20210916-88d6cdcd1f9570140170f79a80e78174"},{"postedOn":"6 days ago","description":"<div><div><p><b>Who We Are</b></p><p>Lifeist_ is a new, bold, and disruptive type of wellness company, striving to connect the world with safe, innovative and often daring pathways to individual definitions of wellness.</p><p>Health &amp; wellness is evolving and becoming increasingly complicated. Lifeist is a global health platform striving to connect the world with safe, innovative and daring pathways to their individual definition of wellness. Whether humans need to find a product that makes them feel relaxed, energetic, productive, or internally healthier, Lifeist will connect them with these innovative solutions and if they don't exist, create them.</p><p>Lifeist’s portfolio of businesses include: CannMart.com which provides Canadian customers with a diverse selection of cannabis products and accessories, and its U.S. customers with hemp-derived CBD and smoking accessories; CannMart’s Canadian recreational cannabis distribution business facilitating sales to a number of provincial government control boards; and CannMart Labs Inc., a state-of-the-art BHO extraction facility set to produce higher margin cannabis concentrate products.</p><p>Our Positioning - <b>Higher Living</b></p><p>Our Mission - <b>To Let The Normal Human Unlock Extraordinary</b></p><p>Our Vision - <b>To Simplify Your Path To Wellness</b></p><p></p><p><b><br />Who You Are</b></p><p>The <b>QA/RA Manager</b><i> </i>will be a key member of CannMart Inc’s. Quality and Regulatory team. The ideal candidate will be quality driven, with a natural ability to problem solve. CannMart is looking for someone who is an excellent communicator, and has a natural ability to work with a variety of people, as well as be a team leader.</p><p><b>Responsibilities</b></p><ul><li>Ensure compliance with applicable regulatory frameworks (e.g. as prescribed by the <i>Cannabis Act</i> and <i>Cannabis Regulations</i>).</li><li>Determine internal best practices and champion a quality culture of excellence.</li><li>Manage the organizational security plan, security clearance applications, changes to key personnel and other communications with the regulator pertaining to physical security and security cleared personnel as well as new licence applications, licence amendments and renewal applications.</li><li>Manage activities performed through the Cannabis Tracking and Licensing System.</li><li>Lead a growing quality and regulatory team through effective relationship management, performance management, training and coaching.</li><li>Ensure that licensed activities are conducted according to standard operating procedures and work instructions and that controlled documents are kept up to date.</li><li>Effective deviation management, including root cause analysis and investigation, corrective action and implementation of quality event reporting.</li><li>Identify key performance indicators that will drive continuous improvement and compliance.</li><li>Train team members on Good Production Practices, Good Documentation Practices, Good Recordkeeping Practices and other quality systems, as required.</li><li>Collaborate with other business leaders as a quality and regulatory stakeholder to ensure operational success.</li><li>Manage vendor qualification and supplier audit activities.</li><li>Continuously improve the electronic quality management system and quality systems processes.</li><li>Represent CannMart during audits and in communications with regulatory authorities and external business partners.</li><li>Support validation and qualification activities, coordinate analytical testing using validated methods and establish a preventive control program.</li><li>Coordinate quality investigations, complaint handling and mock recall activities.</li><li>Additional duties as required from time-to-time</li></ul><p><b>Education &amp; Experience</b></p><ul><li>Bachelor’s degree in the sciences or a combination of relevant education and experience.</li><li>Three or more years of experience in the cannabis industry is preferred.</li><li>Prior experience in vendor management is required.</li><li>Prior experience in a compliance function is required.</li><li>Prior experience in quality investigations is required.</li><li>Prior experience in food safety is an asset.</li><li>Prior experience establishing quality control programs is an asset.</li><li>Prior experience leading validation and qualification is an asset.</li><li>Security clearance or QAP standing with Health Canada is an asset.</li><li>Effective communication skills are required.</li><li>Demonstrated proficiency in problem solving and risk-based decision making.</li><li>Demonstrated leadership skills.</li><li>Demonstrated investigation and auditing proficiency.</li><li>Demonstrated ability to interpret regulatory requirements.</li><li>Demonstrated ability to collaborate with multiple internal and external stakeholders.</li><li>Demonstrated ability to continuously improve quality systems and champion a quality culture.</li></ul><p><b>Personal Traits We Love to See</b></p><ul><li>You show intellectual curiosity</li><li>You demand integrity</li><li>You practise gratitude</li><li>You make meaningful connections</li><li>You are innovative</li></ul><p>This role will be remote, within Ontario, with the ability to attend on-site support to audit and compliance activities as needed (Facility is located in Etobicoke). We thank you for your interest in employment opportunities at Lifeist_. Please note, only the candidates who are selected for an interview will be contacted.Lifeist_ welcomes and encourages applications from people with disabilities. Accommodations are available on request for candidates taking part in all aspects of the selection process.</p><p></p><p>UTV6uR6bxq</p></div></div>","company":{"companyType":"Public/Established","name":"Namaste Technologies","logoUrl":"/logos/namaste-technologies-9eb6b7a0098e7ad0a52503074f6bbbbd.png"},"location":{"address":"Remote"},"frontendLink":"/job-posting/namaste-technologies/qa-ra-manager/6486d4a4cfd5d5b88d7cf9176a66367c","title":"QA/RA Manager","hash":"6486d4a4cfd5d5b88d7cf9176a66367c","postingUrl":"https://ca.indeed.com/job/qara-manager-c0bc8702b6c712a8"},{"employmentType":"Full-time","postedOn":"20 days ago","description":"<div><p>GVB Biopharma is a vertically integrated, global leader in the ever-growing hemp industry. GVB operates two state-of-the-art facilities: a 30,000-square-foot food-grade hemp processing facility in Central Oregon and a 40,000-square-foot white-label consumer product manufacturing facility in Las Vegas, Nevada. GVB also has sales and general administrative offices in California and Colorado and Florida.</p><p>Job Summary: Optimize overall product flow and quality in a safe manner to meet company production objectives through effective and efficient use of resources such as machines, methods, personnel.</p><p>ESSENTIAL DUTIES AND RESPONSIBILITIES. Other assignments, projects, and duties may be required:<br />Personnel:</p><ul><li>Ensure new employees receive requisite production, required safety and hygiene training</li></ul><ul><li>Ensure production employees comply with company regulatory health and safety standards</li></ul><ul><li>Assist with employee recruitment, performance evaluation, promotion, retention and</li></ul><p>termination activities</p><ul><li>Oversee production employee work schedule to ensure appropriate staffing levels</li></ul><ul><li>Manage annual performance reviews and identify training needs</li></ul><ul><li>Supervise the work of production supervisors</li></ul><p>Production</p><ul><li>Oversee production processes of extraction, distillation, isolation, and formulation</li></ul><ul><li>Work with the operations team to plan, schedule, and perform production activities</li></ul><ul><li>Set all production goals for each department and communicate objectives to supervisors,</li></ul><p>leads and the operators.</p><ul><li>Create a production schedule for each department to support the overall production plan</li></ul><ul><li>Establish workflow practices that improve productivity while maintaining quality and safety</li></ul><ul><li>Suggest and implement process improvements to enhance safety, product quality,</li></ul><p>production efficiency and capacity</p><ul><li>Investigate production issues and develop solutions</li></ul><ul><li>Ensure proper housekeeping routines are established in all production areas</li></ul><ul><li>Establish daily basic machine up-keep procedures to support machine availability</li></ul><ul><li>Provide Key Performance Indicators (KPI) to senior management and post-performance</li></ul><p>data for production personnel to review<br />Material:</p><ul><li>Ensure minimum inventory of hemp, ethanol, heptane, and crude are available for</li></ul><p>production needs and ensuring Purchase Order Requests are sent to maintain inventory<br />when necessary</p><ul><li>Ensure purchased materials are stored safely to maintain material integrity</li></ul><ul><li>Track incoming material deliveries and ensure bill of landing/delivery manifests are collected</li></ul><p>and forwarded to accounts payable</p><p>Quality:</p><ul><li>Ensure product meets quality standards and customer specifications</li></ul><ul><li>Work with Quality Assurance to establish and maintain product quality and safety through</li></ul><p>implementation of quality control systems</p><ul><li>Work with QA/QC to identify quality issues and submit non-conforming product (NCP)</li></ul><p>reports for assessment by Material Review Board.</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>8-10 hour shifts</li><li>5 days a week - one weekend day</li></ul><p>Supplemental Pay:</p><ul><li>Bonus pay</li></ul><p>COVID-19 considerations:<br />GVB has measures and regulations in place to ensure the health and wellbeing of our employees. We have established social distancing and mask requirements and have been following all state and local regulations.</p><ul><li>Must be safety oriented and quality-focused</li><li>Ability to synchronize activities of multiple teams to achieve plant productivity goals</li></ul><ul><li>Good organizational skills</li></ul><ul><li>Detail orientated</li></ul><ul><li>Excellent communication, written and verbal skills</li></ul><ul><li>Ability to coach and mentor employees on a one-on-one basis as well as in group settings</li></ul><ul><li>Good mechanical aptitude</li></ul><p>Requirements:</p><ul><li>5+ years experience in manufacturing operations</li></ul><ul><li>2+years experience in supervisory capacity</li></ul><ul><li>Bachelors Degree preferred</li></ul><p>Location: 212 NORTH STREET, Grass Valley, OR 97029</p><p>Job Type: Full-time</p></div>","company":{"companyType":"Private/Startup","name":"Evergreen State Holdings Llc","logoUrl":"/logos/evergreen-state-holdings-llc-472c5fa08bad68be7418ef3aeb015236.png"},"location":{"country":"United States","address":"Grass Valley, OR 97029","city":"Grass Valley","stateProvince":"OR"},"frontendLink":"/job-posting/evergreen-state-holdings-llc/production-manager/88ad965de2daa43291a5d5adbfce006f","title":"Production Manager","hash":"88ad965de2daa43291a5d5adbfce006f","postingUrl":"https://www.indeed.com/job/production-manager-863f9192d9db0b33"},{"employmentType":"Full-time","postedOn":"14 days ago","description":"<div><p>Lead Chocolatier/Production Manager</p><p>As a seasoned chocolatier, you are a specialized chef who creates candies and confections from chocolate, and your work revolves around choosing between varieties of chocolates and accessory ingredients, creating finished candies of all types and sizes.</p><p>Bernard’s Cannabis Creations is a new cannabis edibles brand from Palm Gardens located in Edmonton, Alberta. We are currently seeking an experienced Lead Chocolatier / Production Manager to perform all commercial chocolate production requirements, including gummy production.</p><p>You will be getting trained by and working with world-renowned Chocolatier Bernard Callebaut.</p><p>As a detail-oriented and enthusiastic individual, you will be hands-on working towards developing and adapting cannabis-infused recipes, completing batches from infusion to the finished product as well as training staff, and ensuring quality is first and foremost.</p><p><b>To qualify for this position, you will possess the following skills and attributes:</b></p><p>• College degree/diploma in related food program is preferred</p><p>• 5 years of work experience in manufacturing environment (preferably chocolate or candy), understanding the chemistry and science of chocolate, along with production efficiencies requirements, costs containment/ reduction and equipment</p><p>• Working knowledge of Food Safety and Quality Standards</p><p>• Experience working with automated filling lines</p><p>• Ability to troubleshoot production issues</p><p>• Knowledge with crafting artisan chocolates and specialty items, including tempering, molding, mixing, finishing, and the preparation of ganache and fillings</p><p>• Able to minimize waste, with knowledge of proper storage and handling abilities</p><p>• Strong command of the English language</p><p>• Ability to lead and supervise a team of professionals, overseeing performance an ensuring quality control and safety.</p><p>Think you have what it takes to create amazing cannabis-infused confectionary chocolates and gummies working with a world-renowned chocolatier? Share your resume with us!</p><p>We thank all applicants for their interest; however, only those selected for an interview will be contacted.</p><p>Job Types: Full-time, Permanent</p><p>Salary: $50,000.00-$60,000.00 per year</p><p><b>Additional pay:</b></p><p>• Bonus pay</p><p><b>Benefits:</b></p><p>• On-site parking</p><p>• Paid time off</p><p><b>Schedule:</b></p><p>• 8 hour shift</p><p>• Monday to Friday</p><p><b>Experience:</b></p><p>• baking: 5 years (preferred)</p><p><b>Work remotely:</b></p><p>• No</p></div>","company":{"name":"Bernard's Cannabis Creations"},"location":{"country":"Canada","address":"Canada"},"frontendLink":"/job-posting/bernards-cannabis-creations/chocolatier-and-production-manager/c0eeba4b9fcaa3b654997e3ef2cc6f4a","title":"Chocolatier & Production Manager","hash":"c0eeba4b9fcaa3b654997e3ef2cc6f4a","postingUrl":"https://jobs.laimoon.com/jobs/externalview/27930294"},{"employmentType":"Salary, Full Time","postedOn":"25 days ago","description":"<div><p>GVB Biopharma is a vertically integrated, global leader in the ever-growing hemp industry. GVB operates two state-of-the-art facilities: a 30,000-square-foot food-grade hemp processing facility in Central Oregon and a 40,000-square-foot white-label consumer product manufacturing facility in Las Vegas, Nevada. GVB also has sales and general administrative offices in California and Colorado.</p><p><b>JOB SUMMARY: </b><br />Optimize overall product flow and quality in a safe manner to meet company production objectives through effective and efficient use of resources such as machines, methods, personnel.</p><p><b>ESSENTIAL DUTIES AND RESPONSIBILITIES: </b><br />Other assignments, projects, and duties may be required:</p><p><b>Personnel: </b></p><ul><li>Ensure new employees receive requisite production, required safety, and hygiene training</li><li>Ensure production employees comply with company regulatory health and safety standards</li><li>Assist with employee recruitment, performance evaluation, promotion, retention, and termination activities</li><li>Oversee production employee work schedule to ensure appropriate staffing levels</li><li>Manage annual performance reviews and identify training needs</li><li>Supervise the work of production supervisors Production</li><li>Oversee production processes of extraction, distillation, isolation, and formulation</li><li>Work with the operations team to plan, schedule, and perform production activities</li><li>Set all production goals for each department and communicate objectives to supervisors, leads, and the operators.</li><li>Create a production schedule for each department to support the overall production plan</li><li>Establish workflow practices that improve productivity while maintaining quality and safety</li><li>Suggest and implement process improvements to enhance safety, product quality, production efficiency, and capacity</li><li>Investigate production issues and develop solutions</li><li>Ensure proper housekeeping routines are established in all production areas</li><li>Establish daily basic machine up-keep procedures to support machine availability</li><li>Provide Key Performance Indicators (KPI) to senior management and post-performance data for production personnel to review</li></ul><p>Material:</p><ul><li>Ensure minimum inventory of hemp, ethanol, heptane, and crude are available for production needs and ensuring Purchase Order Requests are sent to maintain inventory when necessary</li><li>Ensure purchased materials are stored safely to maintain material integrity</li><li>Track incoming material deliveries and ensure bill of landing/delivery manifests are collected and forwarded to accounts payable</li></ul><p><b>Quality: </b></p><ul><li>Ensure product meets quality standards and customer specifications</li><li>Work with Quality Assurance to establish and maintain product quality and safety through the implementation of quality control systems</li><li>Work with QA/QC to identify quality issues and submit non-conforming product (NCP) reports for assessment by Material Review Board.</li></ul><p>Qualifications and Skills:</p><ul><li>Must be safety oriented and quality-focused</li><li>Ability to synchronize activities of multiple teams to achieve plant productivity goals</li><li>Good organizational skills</li><li>Detail orientated</li><li>Excellent communication, written and verbal skills</li><li>Ability to coach and mentor employees on a one-on-one basis as well as in group settings</li><li>Good mechanical aptitude</li></ul><p>Requirements:</p><ul><li>5+ years experience in manufacturing operations</li><li>2+years experience in a supervisory capacity</li><li>Bachelors Degree preferred</li></ul><p><b>Job Type: Salary, Full Time</b></p><p>Job Type: Full-time</p><p>Pay: $65,000.00 - $85,000.00 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>10 hour shift</li></ul><p>Supplemental Pay:</p><ul><li>Bonus pay</li></ul><p>Ability to commute/relocate:</p><ul><li>Grass Valley, OR 97029 (Required)</li></ul><p>Education:</p><ul><li>Bachelor's (Preferred)</li></ul><p>Experience:</p><ul><li>Manufacturing Operations: 5 years (Preferred)</li><li>Production Team Management: 2 years (Preferred)</li></ul><p>Work Location:</p><ul><li>One location</li></ul><p>Typical start time:</p><ul><li>8AM</li></ul><p>Typical end time:</p><ul><li>5PM</li></ul><p>This Job Is Ideal for Someone Who Is:</p><ul><li>Dependable -- more reliable than spontaneous</li><li>Adaptable/flexible -- enjoys doing work that requires frequent shifts in direction</li></ul><p>This Company Describes Its Culture as:</p><ul><li>Detail-oriented -- quality and precision-focused</li><li>Innovative -- innovative and risk-taking</li><li>Outcome-oriented -- results-focused with strong performance culture</li></ul><p>Company's website:</p><ul><li>gvbbiopharma.com</li></ul><p>Benefit Conditions:</p><ul><li>Waiting period may apply</li></ul><p>Work Remotely:</p><ul><li>No</li></ul><p>COVID-19 Precaution(s):</p><ul><li>Personal protective equipment provided or required</li><li>Temperature screenings</li><li>Social distancing guidelines in place</li><li>Sanitizing, disinfecting, or cleaning procedures in place</li></ul></div>","company":{"companyType":"Private/Established","name":"GVB Biopharma","logoUrl":"/logos/gvb-biopharma-ec55e466c36a12bccf78758e67009397.jpeg"},"location":{"country":"United States","address":"Biggs Junction, OR","city":"Biggs Junction","stateProvince":"OR"},"frontendLink":"/job-posting/gvb-biopharma/production-manager/c6134c3b8025f63049733e245252f67f","title":"Production Manager","hash":"c6134c3b8025f63049733e245252f67f","postingUrl":"https://www.indeed.com/job/production-manager-88e3a404fa86d819"},{"employmentType":"Salary, Full Time","postedOn":"25 days ago","description":"<div><p>GVB Biopharma is a vertically integrated, global leader in the ever-growing hemp industry. GVB operates two state-of-the-art facilities: a 30,000-square-foot food-grade hemp processing facility in Central Oregon and a 40,000-square-foot white-label consumer product manufacturing facility in Las Vegas, Nevada. GVB also has sales and general administrative offices in California and Colorado.</p><p><b>JOB SUMMARY: </b><br />Optimize overall product flow and quality in a safe manner to meet company production objectives through effective and efficient use of resources such as machines, methods, personnel.</p><p><b>ESSENTIAL DUTIES AND RESPONSIBILITIES: </b><br />Other assignments, projects, and duties may be required:</p><p><b>Personnel: </b></p><ul><li>Ensure new employees receive requisite production, required safety, and hygiene training</li><li>Ensure production employees comply with company regulatory health and safety standards</li><li>Assist with employee recruitment, performance evaluation, promotion, retention, and termination activities</li><li>Oversee production employee work schedule to ensure appropriate staffing levels</li><li>Manage annual performance reviews and identify training needs</li><li>Supervise the work of production supervisors Production</li><li>Oversee production processes of extraction, distillation, isolation, and formulation</li><li>Work with the operations team to plan, schedule, and perform production activities</li><li>Set all production goals for each department and communicate objectives to supervisors, leads, and the operators.</li><li>Create a production schedule for each department to support the overall production plan</li><li>Establish workflow practices that improve productivity while maintaining quality and safety</li><li>Suggest and implement process improvements to enhance safety, product quality, production efficiency, and capacity</li><li>Investigate production issues and develop solutions</li><li>Ensure proper housekeeping routines are established in all production areas</li><li>Establish daily basic machine up-keep procedures to support machine availability</li><li>Provide Key Performance Indicators (KPI) to senior management and post-performance data for production personnel to review</li></ul><p>Material:</p><ul><li>Ensure minimum inventory of hemp, ethanol, heptane, and crude are available for production needs and ensuring Purchase Order Requests are sent to maintain inventory when necessary</li><li>Ensure purchased materials are stored safely to maintain material integrity</li><li>Track incoming material deliveries and ensure bill of landing/delivery manifests are collected and forwarded to accounts payable</li></ul><p><b>Quality: </b></p><ul><li>Ensure product meets quality standards and customer specifications</li><li>Work with Quality Assurance to establish and maintain product quality and safety through the implementation of quality control systems</li><li>Work with QA/QC to identify quality issues and submit non-conforming product (NCP) reports for assessment by Material Review Board.</li></ul><p>Qualifications and Skills:</p><ul><li>Must be safety oriented and quality-focused</li><li>Ability to synchronize activities of multiple teams to achieve plant productivity goals</li><li>Good organizational skills</li><li>Detail orientated</li><li>Excellent communication, written and verbal skills</li><li>Ability to coach and mentor employees on a one-on-one basis as well as in group settings</li><li>Good mechanical aptitude</li></ul><p>Requirements:</p><ul><li>5+ years experience in manufacturing operations</li><li>2+years experience in a supervisory capacity</li><li>Bachelors Degree preferred</li></ul><p><b>Job Type: Salary, Full Time</b></p><p>Job Type: Full-time</p><p>Pay: $65,000.00 - $85,000.00 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>10 hour shift</li></ul><p>Supplemental Pay:</p><ul><li>Bonus pay</li></ul><p>Ability to commute/relocate:</p><ul><li>Grass Valley, OR 97029 (Required)</li></ul><p>Education:</p><ul><li>Bachelor's (Preferred)</li></ul><p>Experience:</p><ul><li>Manufacturing Operations: 5 years (Preferred)</li><li>Production Team Management: 2 years (Preferred)</li></ul><p>Work Location:</p><ul><li>One location</li></ul><p>Typical start time:</p><ul><li>8AM</li></ul><p>Typical end time:</p><ul><li>5PM</li></ul><p>This Job Is Ideal for Someone Who Is:</p><ul><li>Dependable -- more reliable than spontaneous</li><li>Adaptable/flexible -- enjoys doing work that requires frequent shifts in direction</li></ul><p>This Company Describes Its Culture as:</p><ul><li>Detail-oriented -- quality and precision-focused</li><li>Innovative -- innovative and risk-taking</li><li>Outcome-oriented -- results-focused with strong performance culture</li></ul><p>Company's website:</p><ul><li>gvbbiopharma.com</li></ul><p>Benefit Conditions:</p><ul><li>Waiting period may apply</li></ul><p>Work Remotely:</p><ul><li>No</li></ul><p>COVID-19 Precaution(s):</p><ul><li>Personal protective equipment provided or required</li><li>Temperature screenings</li><li>Social distancing guidelines in place</li><li>Sanitizing, disinfecting, or cleaning procedures in place</li></ul></div>","company":{"companyType":"Private/Established","name":"GVB Biopharma","logoUrl":"/logos/gvb-biopharma-ec55e466c36a12bccf78758e67009397.jpeg"},"location":{"country":"United States","address":"Bend, OR","city":"Bend","stateProvince":"OR"},"frontendLink":"/job-posting/gvb-biopharma/production-manager/63c6103cea0f641daf3c4a8c511ccd24","title":"Production Manager","hash":"63c6103cea0f641daf3c4a8c511ccd24","postingUrl":"https://www.indeed.com/job/production-manager-cc6ecd98e8c3ae92"},{"employmentType":"Salary, Full Time","postedOn":"25 days ago","description":"<div><p>GVB Biopharma is a vertically integrated, global leader in the ever-growing hemp industry. GVB operates two state-of-the-art facilities: a 30,000-square-foot food-grade hemp processing facility in Central Oregon and a 40,000-square-foot white-label consumer product manufacturing facility in Las Vegas, Nevada. GVB also has sales and general administrative offices in California and Colorado.</p><p><b>JOB SUMMARY: </b><br />Optimize overall product flow and quality in a safe manner to meet company production objectives through effective and efficient use of resources such as machines, methods, personnel.</p><p><b>ESSENTIAL DUTIES AND RESPONSIBILITIES: </b><br />Other assignments, projects, and duties may be required:</p><p><b>Personnel: </b></p><ul><li>Ensure new employees receive requisite production, required safety, and hygiene training</li><li>Ensure production employees comply with company regulatory health and safety standards</li><li>Assist with employee recruitment, performance evaluation, promotion, retention, and termination activities</li><li>Oversee production employee work schedule to ensure appropriate staffing levels</li><li>Manage annual performance reviews and identify training needs</li><li>Supervise the work of production supervisors Production</li><li>Oversee production processes of extraction, distillation, isolation, and formulation</li><li>Work with the operations team to plan, schedule, and perform production activities</li><li>Set all production goals for each department and communicate objectives to supervisors, leads, and the operators.</li><li>Create a production schedule for each department to support the overall production plan</li><li>Establish workflow practices that improve productivity while maintaining quality and safety</li><li>Suggest and implement process improvements to enhance safety, product quality, production efficiency, and capacity</li><li>Investigate production issues and develop solutions</li><li>Ensure proper housekeeping routines are established in all production areas</li><li>Establish daily basic machine up-keep procedures to support machine availability</li><li>Provide Key Performance Indicators (KPI) to senior management and post-performance data for production personnel to review</li></ul><p>Material:</p><ul><li>Ensure minimum inventory of hemp, ethanol, heptane, and crude are available for production needs and ensuring Purchase Order Requests are sent to maintain inventory when necessary</li><li>Ensure purchased materials are stored safely to maintain material integrity</li><li>Track incoming material deliveries and ensure bill of landing/delivery manifests are collected and forwarded to accounts payable</li></ul><p><b>Quality: </b></p><ul><li>Ensure product meets quality standards and customer specifications</li><li>Work with Quality Assurance to establish and maintain product quality and safety through the implementation of quality control systems</li><li>Work with QA/QC to identify quality issues and submit non-conforming product (NCP) reports for assessment by Material Review Board.</li></ul><p>Qualifications and Skills:</p><ul><li>Must be safety oriented and quality-focused</li><li>Ability to synchronize activities of multiple teams to achieve plant productivity goals</li><li>Good organizational skills</li><li>Detail orientated</li><li>Excellent communication, written and verbal skills</li><li>Ability to coach and mentor employees on a one-on-one basis as well as in group settings</li><li>Good mechanical aptitude</li></ul><p>Requirements:</p><ul><li>5+ years experience in manufacturing operations</li><li>2+years experience in a supervisory capacity</li><li>Bachelors Degree preferred</li></ul><p><b>Job Type: Salary, Full Time</b></p><p>Job Type: Full-time</p><p>Pay: $65,000.00 - $85,000.00 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>10 hour shift</li></ul><p>Supplemental Pay:</p><ul><li>Bonus pay</li></ul><p>Ability to commute/relocate:</p><ul><li>Grass Valley, OR 97029 (Required)</li></ul><p>Education:</p><ul><li>Bachelor's (Preferred)</li></ul><p>Experience:</p><ul><li>Manufacturing Operations: 5 years (Preferred)</li><li>Production Team Management: 2 years (Preferred)</li></ul><p>Work Location:</p><ul><li>One location</li></ul><p>Typical start time:</p><ul><li>8AM</li></ul><p>Typical end time:</p><ul><li>5PM</li></ul><p>This Job Is Ideal for Someone Who Is:</p><ul><li>Dependable -- more reliable than spontaneous</li><li>Adaptable/flexible -- enjoys doing work that requires frequent shifts in direction</li></ul><p>This Company Describes Its Culture as:</p><ul><li>Detail-oriented -- quality and precision-focused</li><li>Innovative -- innovative and risk-taking</li><li>Outcome-oriented -- results-focused with strong performance culture</li></ul><p>Company's website:</p><ul><li>gvbbiopharma.com</li></ul><p>Benefit Conditions:</p><ul><li>Waiting period may apply</li></ul><p>Work Remotely:</p><ul><li>No</li></ul><p>COVID-19 Precaution(s):</p><ul><li>Personal protective equipment provided or required</li><li>Temperature screenings</li><li>Social distancing guidelines in place</li><li>Sanitizing, disinfecting, or cleaning procedures in place</li></ul></div>","company":{"companyType":"Private/Established","name":"GVB Biopharma","logoUrl":"/logos/gvb-biopharma-ec55e466c36a12bccf78758e67009397.jpeg"},"location":{"country":"United States","address":"Lyle, WA","city":"Lyle","stateProvince":"WA"},"frontendLink":"/job-posting/gvb-biopharma/production-manager/3efbefe0f592620e25133d054968b146","title":"Production Manager","hash":"3efbefe0f592620e25133d054968b146","postingUrl":"https://www.indeed.com/job/production-manager-f344ddc71ce02347"},{"employmentType":"Salary, Full Time","postedOn":"25 days ago","description":"<div><p>GVB Biopharma is a vertically integrated, global leader in the ever-growing hemp industry. GVB operates two state-of-the-art facilities: a 30,000-square-foot food-grade hemp processing facility in Central Oregon and a 40,000-square-foot white-label consumer product manufacturing facility in Las Vegas, Nevada. GVB also has sales and general administrative offices in California and Colorado.</p><p><b>JOB SUMMARY: </b><br />Optimize overall product flow and quality in a safe manner to meet company production objectives through effective and efficient use of resources such as machines, methods, personnel.</p><p><b>ESSENTIAL DUTIES AND RESPONSIBILITIES: </b><br />Other assignments, projects, and duties may be required:</p><p><b>Personnel: </b></p><ul><li>Ensure new employees receive requisite production, required safety, and hygiene training</li><li>Ensure production employees comply with company regulatory health and safety standards</li><li>Assist with employee recruitment, performance evaluation, promotion, retention, and termination activities</li><li>Oversee production employee work schedule to ensure appropriate staffing levels</li><li>Manage annual performance reviews and identify training needs</li><li>Supervise the work of production supervisors Production</li><li>Oversee production processes of extraction, distillation, isolation, and formulation</li><li>Work with the operations team to plan, schedule, and perform production activities</li><li>Set all production goals for each department and communicate objectives to supervisors, leads, and the operators.</li><li>Create a production schedule for each department to support the overall production plan</li><li>Establish workflow practices that improve productivity while maintaining quality and safety</li><li>Suggest and implement process improvements to enhance safety, product quality, production efficiency, and capacity</li><li>Investigate production issues and develop solutions</li><li>Ensure proper housekeeping routines are established in all production areas</li><li>Establish daily basic machine up-keep procedures to support machine availability</li><li>Provide Key Performance Indicators (KPI) to senior management and post-performance data for production personnel to review</li></ul><p>Material:</p><ul><li>Ensure minimum inventory of hemp, ethanol, heptane, and crude are available for production needs and ensuring Purchase Order Requests are sent to maintain inventory when necessary</li><li>Ensure purchased materials are stored safely to maintain material integrity</li><li>Track incoming material deliveries and ensure bill of landing/delivery manifests are collected and forwarded to accounts payable</li></ul><p><b>Quality: </b></p><ul><li>Ensure product meets quality standards and customer specifications</li><li>Work with Quality Assurance to establish and maintain product quality and safety through the implementation of quality control systems</li><li>Work with QA/QC to identify quality issues and submit non-conforming product (NCP) reports for assessment by Material Review Board.</li></ul><p>Qualifications and Skills:</p><ul><li>Must be safety oriented and quality-focused</li><li>Ability to synchronize activities of multiple teams to achieve plant productivity goals</li><li>Good organizational skills</li><li>Detail orientated</li><li>Excellent communication, written and verbal skills</li><li>Ability to coach and mentor employees on a one-on-one basis as well as in group settings</li><li>Good mechanical aptitude</li></ul><p>Requirements:</p><ul><li>5+ years experience in manufacturing operations</li><li>2+years experience in a supervisory capacity</li><li>Bachelors Degree preferred</li></ul><p><b>Job Type: Salary, Full Time</b></p><p>Job Type: Full-time</p><p>Pay: $65,000.00 - $85,000.00 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>10 hour shift</li></ul><p>Supplemental Pay:</p><ul><li>Bonus pay</li></ul><p>Ability to commute/relocate:</p><ul><li>Grass Valley, OR 97029 (Required)</li></ul><p>Education:</p><ul><li>Bachelor's (Preferred)</li></ul><p>Experience:</p><ul><li>Manufacturing Operations: 5 years (Preferred)</li><li>Production Team Management: 2 years (Preferred)</li></ul><p>Work Location:</p><ul><li>One location</li></ul><p>Typical start time:</p><ul><li>8AM</li></ul><p>Typical end time:</p><ul><li>5PM</li></ul><p>This Job Is Ideal for Someone Who Is:</p><ul><li>Dependable -- more reliable than spontaneous</li><li>Adaptable/flexible -- enjoys doing work that requires frequent shifts in direction</li></ul><p>This Company Describes Its Culture as:</p><ul><li>Detail-oriented -- quality and precision-focused</li><li>Innovative -- innovative and risk-taking</li><li>Outcome-oriented -- results-focused with strong performance culture</li></ul><p>Company's website:</p><ul><li>gvbbiopharma.com</li></ul><p>Benefit Conditions:</p><ul><li>Waiting period may apply</li></ul><p>Work Remotely:</p><ul><li>No</li></ul><p>COVID-19 Precaution(s):</p><ul><li>Personal protective equipment provided or required</li><li>Temperature screenings</li><li>Social distancing guidelines in place</li><li>Sanitizing, disinfecting, or cleaning procedures in place</li></ul></div>","company":{"companyType":"Private/Established","name":"GVB Biopharma","logoUrl":"/logos/gvb-biopharma-ec55e466c36a12bccf78758e67009397.jpeg"},"location":{"country":"United States","address":"The Dalles, OR","city":"The Dalles","stateProvince":"OR"},"frontendLink":"/job-posting/gvb-biopharma/production-manager/57f6dfce20b0fd53bb2889e247df2d4d","title":"Production Manager","hash":"57f6dfce20b0fd53bb2889e247df2d4d","postingUrl":"https://www.indeed.com/job/production-manager-73e6f51df87a01ac"},{"employmentType":"Salary, Full Time","postedOn":"25 days ago","description":"<div><p>GVB Biopharma is a vertically integrated, global leader in the ever-growing hemp industry. GVB operates two state-of-the-art facilities: a 30,000-square-foot food-grade hemp processing facility in Central Oregon and a 40,000-square-foot white-label consumer product manufacturing facility in Las Vegas, Nevada. GVB also has sales and general administrative offices in California and Colorado.</p><p><b>JOB SUMMARY: </b><br />Optimize overall product flow and quality in a safe manner to meet company production objectives through effective and efficient use of resources such as machines, methods, personnel.</p><p><b>ESSENTIAL DUTIES AND RESPONSIBILITIES: </b><br />Other assignments, projects, and duties may be required:</p><p><b>Personnel: </b></p><ul><li>Ensure new employees receive requisite production, required safety, and hygiene training</li><li>Ensure production employees comply with company regulatory health and safety standards</li><li>Assist with employee recruitment, performance evaluation, promotion, retention, and termination activities</li><li>Oversee production employee work schedule to ensure appropriate staffing levels</li><li>Manage annual performance reviews and identify training needs</li><li>Supervise the work of production supervisors Production</li><li>Oversee production processes of extraction, distillation, isolation, and formulation</li><li>Work with the operations team to plan, schedule, and perform production activities</li><li>Set all production goals for each department and communicate objectives to supervisors, leads, and the operators.</li><li>Create a production schedule for each department to support the overall production plan</li><li>Establish workflow practices that improve productivity while maintaining quality and safety</li><li>Suggest and implement process improvements to enhance safety, product quality, production efficiency, and capacity</li><li>Investigate production issues and develop solutions</li><li>Ensure proper housekeeping routines are established in all production areas</li><li>Establish daily basic machine up-keep procedures to support machine availability</li><li>Provide Key Performance Indicators (KPI) to senior management and post-performance data for production personnel to review</li></ul><p>Material:</p><ul><li>Ensure minimum inventory of hemp, ethanol, heptane, and crude are available for production needs and ensuring Purchase Order Requests are sent to maintain inventory when necessary</li><li>Ensure purchased materials are stored safely to maintain material integrity</li><li>Track incoming material deliveries and ensure bill of landing/delivery manifests are collected and forwarded to accounts payable</li></ul><p><b>Quality: </b></p><ul><li>Ensure product meets quality standards and customer specifications</li><li>Work with Quality Assurance to establish and maintain product quality and safety through the implementation of quality control systems</li><li>Work with QA/QC to identify quality issues and submit non-conforming product (NCP) reports for assessment by Material Review Board.</li></ul><p>Qualifications and Skills:</p><ul><li>Must be safety oriented and quality-focused</li><li>Ability to synchronize activities of multiple teams to achieve plant productivity goals</li><li>Good organizational skills</li><li>Detail orientated</li><li>Excellent communication, written and verbal skills</li><li>Ability to coach and mentor employees on a one-on-one basis as well as in group settings</li><li>Good mechanical aptitude</li></ul><p>Requirements:</p><ul><li>5+ years experience in manufacturing operations</li><li>2+years experience in a supervisory capacity</li><li>Bachelors Degree preferred</li></ul><p><b>Job Type: Salary, Full Time</b></p><p>Job Type: Full-time</p><p>Pay: $65,000.00 - $85,000.00 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>10 hour shift</li></ul><p>Supplemental Pay:</p><ul><li>Bonus pay</li></ul><p>Ability to commute/relocate:</p><ul><li>Grass Valley, OR 97029 (Required)</li></ul><p>Education:</p><ul><li>Bachelor's (Preferred)</li></ul><p>Experience:</p><ul><li>Manufacturing Operations: 5 years (Preferred)</li><li>Production Team Management: 2 years (Preferred)</li></ul><p>Work Location:</p><ul><li>One location</li></ul><p>Typical start time:</p><ul><li>8AM</li></ul><p>Typical end time:</p><ul><li>5PM</li></ul><p>This Job Is Ideal for Someone Who Is:</p><ul><li>Dependable -- more reliable than spontaneous</li><li>Adaptable/flexible -- enjoys doing work that requires frequent shifts in direction</li></ul><p>This Company Describes Its Culture as:</p><ul><li>Detail-oriented -- quality and precision-focused</li><li>Innovative -- innovative and risk-taking</li><li>Outcome-oriented -- results-focused with strong performance culture</li></ul><p>Company's website:</p><ul><li>gvbbiopharma.com</li></ul><p>Benefit Conditions:</p><ul><li>Waiting period may apply</li></ul><p>Work Remotely:</p><ul><li>No</li></ul><p>COVID-19 Precaution(s):</p><ul><li>Personal protective equipment provided or required</li><li>Temperature screenings</li><li>Social distancing guidelines in place</li><li>Sanitizing, disinfecting, or cleaning procedures in place</li></ul></div>","company":{"companyType":"Private/Established","name":"GVB Biopharma","logoUrl":"/logos/gvb-biopharma-ec55e466c36a12bccf78758e67009397.jpeg"},"location":{"country":"United States","address":"Hood River, OR","city":"Hood River","stateProvince":"OR"},"frontendLink":"/job-posting/gvb-biopharma/production-manager/b75487f1660c92dbe332ae89da6af6b1","title":"Production Manager","hash":"b75487f1660c92dbe332ae89da6af6b1","postingUrl":"https://www.indeed.com/job/production-manager-3a233ca1832d782d"},{"employmentType":"Salary, Full Time","postedOn":"25 days ago","description":"<div><p>GVB Biopharma is a vertically integrated, global leader in the ever-growing hemp industry. GVB operates two state-of-the-art facilities: a 30,000-square-foot food-grade hemp processing facility in Central Oregon and a 40,000-square-foot white-label consumer product manufacturing facility in Las Vegas, Nevada. GVB also has sales and general administrative offices in California and Colorado.</p><p><b>JOB SUMMARY: </b><br />Optimize overall product flow and quality in a safe manner to meet company production objectives through effective and efficient use of resources such as machines, methods, personnel.</p><p><b>ESSENTIAL DUTIES AND RESPONSIBILITIES: </b><br />Other assignments, projects, and duties may be required:</p><p><b>Personnel: </b></p><ul><li>Ensure new employees receive requisite production, required safety, and hygiene training</li><li>Ensure production employees comply with company regulatory health and safety standards</li><li>Assist with employee recruitment, performance evaluation, promotion, retention, and termination activities</li><li>Oversee production employee work schedule to ensure appropriate staffing levels</li><li>Manage annual performance reviews and identify training needs</li><li>Supervise the work of production supervisors Production</li><li>Oversee production processes of extraction, distillation, isolation, and formulation</li><li>Work with the operations team to plan, schedule, and perform production activities</li><li>Set all production goals for each department and communicate objectives to supervisors, leads, and the operators.</li><li>Create a production schedule for each department to support the overall production plan</li><li>Establish workflow practices that improve productivity while maintaining quality and safety</li><li>Suggest and implement process improvements to enhance safety, product quality, production efficiency, and capacity</li><li>Investigate production issues and develop solutions</li><li>Ensure proper housekeeping routines are established in all production areas</li><li>Establish daily basic machine up-keep procedures to support machine availability</li><li>Provide Key Performance Indicators (KPI) to senior management and post-performance data for production personnel to review</li></ul><p>Material:</p><ul><li>Ensure minimum inventory of hemp, ethanol, heptane, and crude are available for production needs and ensuring Purchase Order Requests are sent to maintain inventory when necessary</li><li>Ensure purchased materials are stored safely to maintain material integrity</li><li>Track incoming material deliveries and ensure bill of landing/delivery manifests are collected and forwarded to accounts payable</li></ul><p><b>Quality: </b></p><ul><li>Ensure product meets quality standards and customer specifications</li><li>Work with Quality Assurance to establish and maintain product quality and safety through the implementation of quality control systems</li><li>Work with QA/QC to identify quality issues and submit non-conforming product (NCP) reports for assessment by Material Review Board.</li></ul><p>Qualifications and Skills:</p><ul><li>Must be safety oriented and quality-focused</li><li>Ability to synchronize activities of multiple teams to achieve plant productivity goals</li><li>Good organizational skills</li><li>Detail orientated</li><li>Excellent communication, written and verbal skills</li><li>Ability to coach and mentor employees on a one-on-one basis as well as in group settings</li><li>Good mechanical aptitude</li></ul><p>Requirements:</p><ul><li>5+ years experience in manufacturing operations</li><li>2+years experience in a supervisory capacity</li><li>Bachelors Degree preferred</li></ul><p><b>Job Type: Salary, Full Time</b></p><p>Job Type: Full-time</p><p>Pay: $65,000.00 - $85,000.00 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>10 hour shift</li></ul><p>Supplemental Pay:</p><ul><li>Bonus pay</li></ul><p>Ability to commute/relocate:</p><ul><li>Grass Valley, OR 97029 (Required)</li></ul><p>Education:</p><ul><li>Bachelor's (Preferred)</li></ul><p>Experience:</p><ul><li>Manufacturing Operations: 5 years (Preferred)</li><li>Production Team Management: 2 years (Preferred)</li></ul><p>Work Location:</p><ul><li>One location</li></ul><p>Typical start time:</p><ul><li>8AM</li></ul><p>Typical end time:</p><ul><li>5PM</li></ul><p>This Job Is Ideal for Someone Who Is:</p><ul><li>Dependable -- more reliable than spontaneous</li><li>Adaptable/flexible -- enjoys doing work that requires frequent shifts in direction</li></ul><p>This Company Describes Its Culture as:</p><ul><li>Detail-oriented -- quality and precision-focused</li><li>Innovative -- innovative and risk-taking</li><li>Outcome-oriented -- results-focused with strong performance culture</li></ul><p>Company's website:</p><ul><li>gvbbiopharma.com</li></ul><p>Benefit Conditions:</p><ul><li>Waiting period may apply</li></ul><p>Work Remotely:</p><ul><li>No</li></ul><p>COVID-19 Precaution(s):</p><ul><li>Personal protective equipment provided or required</li><li>Temperature screenings</li><li>Social distancing guidelines in place</li><li>Sanitizing, disinfecting, or cleaning procedures in place</li></ul></div>","company":{"companyType":"Private/Established","name":"GVB Biopharma","logoUrl":"/logos/gvb-biopharma-ec55e466c36a12bccf78758e67009397.jpeg"},"location":{"country":"United States","address":"Moro, OR","city":"Moro","stateProvince":"OR"},"frontendLink":"/job-posting/gvb-biopharma/production-manager/e60eea7e26eeecaeb3b1139e54dcd096","title":"Production Manager","hash":"e60eea7e26eeecaeb3b1139e54dcd096","postingUrl":"https://www.indeed.com/job/production-manager-e7b8ac3a91ada344"}]