Cannabis Quality Assurance Manager Testing Lab Jobs
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Here are 5 cannabis jobs mentioning "quality assurance manager testing lab" in May 2024, at companies like RDP Development, and CERESLabs, including positions such as Quality Assurance Manager - Testing Lab, and Quality Assurance Manager - Cannabis Analytical Testing Lab.
More than 30+ days
We are a Cannabis Testing Lab based in Las Vegas. Our goal is to protect patients and consumers by certifying that the product they are consuming have undergone the same level of stringent testing as other drug and food products.
Quality Manager
Responsibilities within the ISO 17025:2017 Quality Management System
The Quality Manager has defined responsibility and authority for ensuring that the quality management system related to quality in the laboratory is implemented and followed at all times. The Quality Manager has direct access to the highest level of management where decisions are made on laboratory policy or resources.
The Quality Manager maintains the master list identifying
the current revision status and distribution of documents in the QMS to prevent the use of obsolete documents.
Required Qualifications, Training & Skills
Must be self-motivated, energetic and possess the ability to work in a diverse GLP laboratory environment under a QMS. Candidate must have deep understanding of analytical techniques with hands-on experience in method development leading to the creation of SOPs, LIMS interface and basic chemistry techniques e.g. HPLC, GC-MS, LC-MS.
This position requires the candidates to have adequate statistical analysis skills, good concept of quantification, accuracy/variation, and organizational skills. Candidates must have the ability to work independently with minimal supervision; have strong trouble-shooting, computer and record keeping skills and problem-solving skills.
Specifically
- Serves as the focal point for the QMS
- Oversees and provides secondary approval for all certificates of analyses published by lab
- Approves all controlled laboratory documentation
- Oversees quality control data.
- Evaluates data objectively and performs assessments without managerial influence.
- Maintains ISO 17025 accreditation and compliance with State and local regulatory requirements, including quality checks and compliance of safety standards such as, but not limited to, OSHA, Fire Marshall and Police
- Oversees the Quality Assurance and Control Program
- Manages and maintains all laboratory controlled documentation
- Performs internal audits, including both technical and quality systems and direct any necessary corrective action notifying management of deficiencies or opportunities for improvement
- Develops and maintains laboratory policy and procedural manuals, quality procedures, SOPs, equipment requirements, and evaluating and implementing new procedures as necessary.
- Performs, schedules, and records internal laboratory inspections as necessary
- Oversees the LIMS and general records management.
- Provides oversight of human resources and any adherences required as an equal opportunity facility
- Serves as the laboratory safety officer with oversight on all safety systems in adherence with ISO 17025, OSHA, NAC 453A, and any other laboratory safety organizations
- Maintains chemical/equipment traceability records and generating control charts.
- Maintains training records for all lab staff.
- Generates training plans for all laboratory staff.
- Creates and maintains internal training processes for all laboratory staff including (but not limited to) any necessary retrainings, safety training, good laboratory practices, quality assurance programs, and continuing education
- Schedules proficiency testing for all analytes
- Monitors CAPAs, non-conformances, OOS, failed tests, repeat tests employee incidents, and client complaints for areas of improvement
- May oversee and sign-off on any laboratory documentation as needed
- May step in and perform any tasks assigned in the lab as needed
Desired Skills
Demonstrated expertise in sample chain of custody protocols, large dataset analysis, should be aware of emerging analytical techniques, experience using LIMS, familiar with cGMP and GLP requirements, as well as working under a Quality Management System are favored.
Required Education, Expertise & Experience
A Bachelor’s Degree (BS) or greater in chemistry, biochemistry, microbiology or equivalent with 5 years of relevant experience is REQUIRED.
Excellent written and oral communication skills, previously demonstrated successful managerial or supervisory experience and previously demonstrated successful ability to contribute in a team Quality Management System environment are essential.
Job Type: Full-time
Pay: $50,000.00 - $75,000.00 per year
Benefits:
- Health insurance
- Paid time off
Schedule:
- Monday to Friday
Experience:
- ISO 9001: 3 years (Preferred)
- Quality assurance: 4 years (Preferred)
- Quality control: 4 years (Preferred)
- lab: 4 years (Preferred)
Work Location: One location
Apply for this job with RDP Development
Apply now →
By clicking the "Apply now" button, you'll be leaving Fazow and going to an external job application page for this company.
Please research all companies before applying. When applying for jobs, you should NOT have to pay to apply.
Fazow accepts no liability or responsibility as a consequence of any reliance upon information on external sites or in jobs listed on fazow.com.
We are a Cannabis Testing Lab based in Las Vegas. Our goal is to protect patients and consumers by certifying that the product they are consuming have undergone the same level of stringent testing as other drug and food products.
Quality Manager
Responsibilities within the ISO 17025:2017 Quality Management System
The Quality Manager has defined responsibility and authority for ensuring that the quality management system related to quality in the laboratory is implemented and followed at all times. The Quality Manager has direct access to the highest level of management where decisions are made on laboratory policy or resources.
The Quality Manager maintains the master list identifying
the current revision status and distribution of documents in the QMS to prevent the use of obsolete documents.
Required Qualifications, Training & Skills
Must be self-motivated, energetic and possess the ability to work in a diverse GLP laboratory environment under a QMS. Candidate must have deep understanding of analytical techniques with hands-on experience in method development leading to the creation of SOPs, LIMS interface and basic chemistry techniques e.g. HPLC, GC-MS, LC-MS.
This position requires the candidates to have adequate statistical analysis skills, good concept of quantification, accuracy/variation, and organizational skills. Candidates must have the ability to work independently with minimal supervision; have strong trouble-shooting, computer and record keeping skills and problem-solving skills.
Specifically
- Serves as the focal point for the QMS
- Oversees and provides secondary approval for all certificates of analyses published by lab
- Approves all controlled laboratory documentation
- Oversees quality control data.
- Evaluates data objectively and performs assessments without managerial influence.
- Maintains ISO 17025 accreditation and compliance with State and local regulatory requirements, including quality checks and compliance of safety standards such as, but not limited to, OSHA, Fire Marshall and Police
- Oversees the Quality Assurance and Control Program
- Manages and maintains all laboratory controlled documentation
- Performs internal audits, including both technical and quality systems and direct any necessary corrective action notifying management of deficiencies or opportunities for improvement
- Develops and maintains laboratory policy and procedural manuals, quality procedures, SOPs, equipment requirements, and evaluating and implementing new procedures as necessary.
- Performs, schedules, and records internal laboratory inspections as necessary
- Oversees the LIMS and general records management.
- Provides oversight of human resources and any adherences required as an equal opportunity facility
- Serves as the laboratory safety officer with oversight on all safety systems in adherence with ISO 17025, OSHA, NAC 453A, and any other laboratory safety organizations
- Maintains chemical/equipment traceability records and generating control charts.
- Maintains training records for all lab staff.
- Generates training plans for all laboratory staff.
- Creates and maintains internal training processes for all laboratory staff including (but not limited to) any necessary retrainings, safety training, good laboratory practices, quality assurance programs, and continuing education
- Schedules proficiency testing for all analytes
- Monitors CAPAs, non-conformances, OOS, failed tests, repeat tests employee incidents, and client complaints for areas of improvement
- May oversee and sign-off on any laboratory documentation as needed
- May step in and perform any tasks assigned in the lab as needed
Desired Skills
Demonstrated expertise in sample chain of custody protocols, large dataset analysis, should be aware of emerging analytical techniques, experience using LIMS, familiar with cGMP and GLP requirements, as well as working under a Quality Management System are favored.
Required Education, Expertise & Experience
A Bachelor’s Degree (BS) or greater in chemistry, biochemistry, microbiology or equivalent with 5 years of relevant experience is REQUIRED.
Excellent written and oral communication skills, previously demonstrated successful managerial or supervisory experience and previously demonstrated successful ability to contribute in a team Quality Management System environment are essential.
Job Type: Full-time
Pay: $50,000.00 - $75,000.00 per year
Benefits:
- Health insurance
- Paid time off
Schedule:
- Monday to Friday
Experience:
- ISO 9001: 3 years (Preferred)
- Quality assurance: 4 years (Preferred)
- Quality control: 4 years (Preferred)
- lab: 4 years (Preferred)
Work Location: One location
Apply for this job with RDP Development
Apply now →
By clicking the "Apply now" button, you'll be leaving Fazow and going to an external job application page for this company.
Please research all companies before applying. When applying for jobs, you should NOT have to pay to apply.
Fazow accepts no liability or responsibility as a consequence of any reliance upon information on external sites or in jobs listed on fazow.com.
We are a Cannabis Testing Lab based in Las Vegas. Our goal is to protect patients and consumers by certifying that the product they are consuming have undergone the same level of stringent testing as other drug and food products.
Quality Manager
Responsibilities within the ISO 17025:2017 Quality Management System
The Quality Manager has defined responsibility and authority for ensuring that the quality management system related to quality in the laboratory is implemented and followed at all times. The Quality Manager has direct access to the highest level of management where decisions are made on laboratory policy or resources.
The Quality Manager maintains the master list identifying
the current revision status and distribution of documents in the QMS to prevent the use of obsolete documents.
Required Qualifications, Training & Skills
Must be self-motivated, energetic and possess the ability to work in a diverse GLP laboratory environment under a QMS. Candidate must have deep understanding of analytical techniques with hands-on experience in method development leading to the creation of SOPs, LIMS interface and basic chemistry techniques e.g. HPLC, GC-MS, LC-MS.
This position requires the candidates to have adequate statistical analysis skills, good concept of quantification, accuracy/variation, and organizational skills. Candidates must have the ability to work independently with minimal supervision; have strong trouble-shooting, computer and record keeping skills and problem-solving skills.
Specifically
- Serves as the focal point for the QMS
- Oversees and provides secondary approval for all certificates of analyses published by lab
- Approves all controlled laboratory documentation
- Oversees quality control data.
- Evaluates data objectively and performs assessments without managerial influence.
- Maintains ISO 17025 accreditation and compliance with State and local regulatory requirements, including quality checks and compliance of safety standards such as, but not limited to, OSHA, Fire Marshall and Police
- Oversees the Quality Assurance and Control Program
- Manages and maintains all laboratory controlled documentation
- Performs internal audits, including both technical and quality systems and direct any necessary corrective action notifying management of deficiencies or opportunities for improvement
- Develops and maintains laboratory policy and procedural manuals, quality procedures, SOPs, equipment requirements, and evaluating and implementing new procedures as necessary.
- Performs, schedules, and records internal laboratory inspections as necessary
- Oversees the LIMS and general records management.
- Provides oversight of human resources and any adherences required as an equal opportunity facility
- Serves as the laboratory safety officer with oversight on all safety systems in adherence with ISO 17025, OSHA, NAC 453A, and any other laboratory safety organizations
- Maintains chemical/equipment traceability records and generating control charts.
- Maintains training records for all lab staff.
- Generates training plans for all laboratory staff.
- Creates and maintains internal training processes for all laboratory staff including (but not limited to) any necessary retrainings, safety training, good laboratory practices, quality assurance programs, and continuing education
- Schedules proficiency testing for all analytes
- Monitors CAPAs, non-conformances, OOS, failed tests, repeat tests employee incidents, and client complaints for areas of improvement
- May oversee and sign-off on any laboratory documentation as needed
- May step in and perform any tasks assigned in the lab as needed
Desired Skills
Demonstrated expertise in sample chain of custody protocols, large dataset analysis, should be aware of emerging analytical techniques, experience using LIMS, familiar with cGMP and GLP requirements, as well as working under a Quality Management System are favored.
Required Education, Expertise & Experience
A Bachelor’s Degree (BS) or greater in chemistry, biochemistry, microbiology or equivalent with 5 years of relevant experience is REQUIRED.
Excellent written and oral communication skills, previously demonstrated successful managerial or supervisory experience and previously demonstrated successful ability to contribute in a team Quality Management System environment are essential.
Job Type: Full-time
Pay: $45,000.00 - $60,000.00 per year
Benefits:
- Health insurance
- Paid time off
Schedule:
- Monday to Friday
Ability to commute/relocate:
- Las Vegas, NV 89102: Reliably commute or planning to relocate before starting work (Preferred)
Experience:
- ISO 9001: 1 year (Preferred)
Work Location: One location
Apply for this job with RDP Development
Apply now →
By clicking the "Apply now" button, you'll be leaving Fazow and going to an external job application page for this company.
Please research all companies before applying. When applying for jobs, you should NOT have to pay to apply.
Fazow accepts no liability or responsibility as a consequence of any reliance upon information on external sites or in jobs listed on fazow.com.
We are a Cannabis Testing Lab based in Las Vegas. Our goal is to protect patients and consumers by certifying that the product they are consuming have undergone the same level of stringent testing as other drug and food products.
Quality Manager
Responsibilities within the ISO 17025:2017 Quality Management System
The Quality Manager has defined responsibility and authority for ensuring that the quality management system related to quality in the laboratory is implemented and followed at all times. The Quality Manager has direct access to the highest level of management where decisions are made on laboratory policy or resources.
The Quality Manager maintains the master list identifying
the current revision status and distribution of documents in the QMS to prevent the use of obsolete documents.
Required Qualifications, Training & Skills
Must be self-motivated, energetic and possess the ability to work in a diverse GLP laboratory environment under a QMS. Candidate must have deep understanding of analytical techniques with hands-on experience in method development leading to the creation of SOPs, LIMS interface and basic chemistry techniques e.g. HPLC, GC-MS, LC-MS.
This position requires the candidates to have adequate statistical analysis skills, good concept of quantification, accuracy/variation, and organizational skills. Candidates must have the ability to work independently with minimal supervision; have strong trouble-shooting, computer and record keeping skills and problem-solving skills.
Specifically
- Serves as the focal point for the QMS
- Oversees and provides secondary approval for all certificates of analyses published by lab
- Approves all controlled laboratory documentation
- Oversees quality control data.
- Evaluates data objectively and performs assessments without managerial influence.
- Maintains ISO 17025 accreditation and compliance with State and local regulatory requirements, including quality checks and compliance of safety standards such as, but not limited to, OSHA, Fire Marshall and Police
- Oversees the Quality Assurance and Control Program
- Manages and maintains all laboratory controlled documentation
- Performs internal audits, including both technical and quality systems and direct any necessary corrective action notifying management of deficiencies or opportunities for improvement
- Develops and maintains laboratory policy and procedural manuals, quality procedures, SOPs, equipment requirements, and evaluating and implementing new procedures as necessary.
- Performs, schedules, and records internal laboratory inspections as necessary
- Oversees the LIMS and general records management.
- Provides oversight of human resources and any adherences required as an equal opportunity facility
- Serves as the laboratory safety officer with oversight on all safety systems in adherence with ISO 17025, OSHA, NAC 453A, and any other laboratory safety organizations
- Maintains chemical/equipment traceability records and generating control charts.
- Maintains training records for all lab staff.
- Generates training plans for all laboratory staff.
- Creates and maintains internal training processes for all laboratory staff including (but not limited to) any necessary retrainings, safety training, good laboratory practices, quality assurance programs, and continuing education
- Schedules proficiency testing for all analytes
- Monitors CAPAs, non-conformances, OOS, failed tests, repeat tests employee incidents, and client complaints for areas of improvement
- May oversee and sign-off on any laboratory documentation as needed
- May step in and perform any tasks assigned in the lab as needed
Desired Skills
Demonstrated expertise in sample chain of custody protocols, large dataset analysis, should be aware of emerging analytical techniques, experience using LIMS, familiar with cGMP and GLP requirements, as well as working under a Quality Management System are favored.
Required Education, Expertise & Experience
A Bachelor’s Degree (BS) or greater in chemistry, biochemistry, microbiology or equivalent with 5 years of relevant experience is REQUIRED.
Excellent written and oral communication skills, previously demonstrated successful managerial or supervisory experience and previously demonstrated successful ability to contribute in a team Quality Management System environment are essential.
Job Type: Full-time
Pay: $45,000.00 - $60,000.00 per year
Benefits:
- Health insurance
- Paid time off
Schedule:
- Monday to Friday
Ability to commute/relocate:
- Las Vegas, NV 89102: Reliably commute or planning to relocate before starting work (Preferred)
Experience:
- ISO 9001: 1 year (Preferred)
Work Location: One location
Apply for this job with RDP Development
Apply now →
By clicking the "Apply now" button, you'll be leaving Fazow and going to an external job application page for this company.
Please research all companies before applying. When applying for jobs, you should NOT have to pay to apply.
Fazow accepts no liability or responsibility as a consequence of any reliance upon information on external sites or in jobs listed on fazow.com.
Quality Assurance Manager - Cannabis Analytical Testing Lab
CERESLabs
4 years ago
Quality Manager – Cannabis Analytical Testing Lab
Responsibilities
Reporting directly to the Chief Executive Officer (CEO), the Quality Manager will serve as the administrator of the Quality Management System (QMS) and the primary point of contact regarding documentation and ISO accreditation.
Working with the Laboratory Director, the Quality Manager will define and implement the technology and systems required to track laboratory activity in accordance withISO 17025 and other accrediting/licensing bodies. The Quality Manager drives the advancement of client safety, developing accurate testing Standard OperatingProcedures (SOPs) with the Laboratory Director by rigorously and creatively applying their scientific knowledge, expertise and Lab experience. The Quality Manager possesses and leverages his or her credibility to inform and influence, leads activities on cannabis, provide insights for the proper procedures for handling samples to be tested and reporting results to the sampled cultivators and/or processors. The QualityManager shall be responsible for training and oversight supervision of all laboratory staff in order to ensure that the laboratory achieves and maintains quality standards of practice.
RESPONSIBILITIES:
- Attend and participate in professional group meetings or continued education activities; staying abreast of new trends and innovations in analytical science
- Lead a team of talented scientists and Lab Techs, growing and attracting top scientific talent
- Provides high-level commentary on vital complaints. Responds to crises involving cannabis complaints. Communicates with outside industry entities as needed.
- Proactively identifies need for analysis of potential safety issue. Communicates results of analysis to Chief Executive Officer as needed.
- Serves as an advisor in management review meetings.
REQUIREMENTS:
- Ph.D. preferred
- Extensive(solid-state) analytical materials characterization and method development
- 3+ years of Management experience in a Certified Laboratory
- Collaborative team player, comfortable leading as well as executing projects
- Driven leader, comfortable in an entrepreneurial, fast-paced, high-energy environment, able to meet multiple deadlines
- Ability to mentor and grow scientific talent
- Excellent interpersonal, verbal, managerial, and written communication skills
Job Type: Full-time
Experience:
- Laboratory Management: 3 years (Preferred)
Education:
- Doctorate (Preferred)
Location:
- Greenfield, CA 93927 (Required)
Work Location:
- One location
Benefits:
- Health insurance
- Paid time off
This Job Is Ideal for Someone Who Is:
- Dependable -- more reliable than spontaneous
- Detail-oriented -- would rather focus on the details of work than the bigger picture
- Autonomous/Independent -- enjoys working with little direction
Schedule:
- Monday to Friday
Apply for this job with CERESLabs
Apply now →
By clicking the "Apply now" button, you'll be leaving Fazow and going to an external job application page for this company.
Please research all companies before applying. When applying for jobs, you should NOT have to pay to apply.
Fazow accepts no liability or responsibility as a consequence of any reliance upon information on external sites or in jobs listed on fazow.com.