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Eurofins

Global lab testing and analytics network

Quality Assurance Manager

Validation, Compliance & Quality SystemsConfirmed live in the last 24 hours
Full-timeVaughan, ON, Canada

About the Job

Requirements

  • A university degree or college diploma in Cannabis, Quality Assurance, or Laboratory Technician.
  • At least 5 years of Quality Assurance experience in an ISO/GMP environment.
  • Strong knowledge of ISO 17025 and experience leading a lab through an ISO 17025 audit.
  • Ability to manage and motivate others, work within a team, and lead the lab/QA team to achieve objectives.
  • Proficiency in Microsoft Office Suite, LIMS, Excel, database user interfaces, and query software.
  • Effective time management and communication skills, with meticulous document review skills.
  • Demonstrated strong knowledge of GMP requirements.
  • Must be able to reliably commute to or relocate to Woodbridge, Ontario, before starting work.
  • Does not require sponsorship to work in Canada.
  • At least 3 years working in Quality Assurance in an ISO/GMP-regulated environment.
  • At least 2 years working in a management position with at least 2 direct reports.
  • At least 2 years of Regulatory Affairs experience.
  • May be required to pass a background check and education/employment verification.

Responsibilities

  • Maintain and continuously improve the Quality Management System (QMS).
  • Ensure all documentation, including SOPs, policies, and records, is controlled and audit ready.
  • Oversee change control, deviations, CAPA, and internal audits.
  • Implement OOS, OOE, and OOT investigations in the QMS.
  • Manage data retention according to existing SOPs.
  • Update the Quality Manual, validation master plan, and training matrix in ISOlocity (QMS).
  • Ensure compliance with ISO 17025 standards for laboratory competence.
  • Oversee equipment calibrations and IQ/OQ/PQ of all critical equipment.
  • Coordinate with the accrediting body during assessments and renewals.
  • Maintain the proficiency testing plan according to the ISO 17025 scope of accreditation.
  • Ensure proper audit trails are in place for all critical equipment.
  • Maintain equipment user accounts in coordination with IT in accordance with GMP compliance.
  • Implement data integrity policies aligned with ALCOA+ principles.
  • Provide logbooks to the laboratory and manage logbook inventory.
  • Collaborate with the IT department on data governance.
  • Review pest control and sanitation reports.
  • Manage the lab’s licensing requirements with cannabis regulators, including state cannabis authorities and Health Canada.
  • Prepare and submit documentation for new licenses, renewals, amendments, or relocations.
  • Ensure testing complies with local cannabis regulations and international limits for potency, residual solvents, pesticides, heavy metals, and other applicable analytes.
  • Monitor testing limits, methods, and client reporting against current rules in the Index of Testing.
  • Maintain all redacted and summary reports.
  • Ensure obsolete or archived document versions are unavailable to laboratory personnel and the client care team.
  • Lead regulatory inspections from clients or accreditors.
  • Conduct internal audits and maintain site inspection readiness.
  • Coordinate and respond to notices of non-compliance or corrective action requests.
  • Monitor changes in testing regulations, limits, and accreditation requirements.
  • Communicate relevant regulatory updates to laboratory staff and leadership.
  • Coordinate with the Lab Head to adjust laboratory procedures and testing panels accordingly.
  • Act as the point of contact with regulatory agencies.
  • Submit incident reports, compliance reports, or change notifications when required.
  • Support client communication related to compliance or regulatory interpretation.
  • Lead the QA/RA team and coordinate with the Lab Director and Executive team.
  • Conduct yearly performance reviews and define goals for team members.
  • Provide QA training to laboratory personnel on quality assurance protocols, regulatory compliance, and best practices.
  • Establish and monitor quality KPIs and regulatory compliance metrics.
  • Approve all vendors used for the laboratory, cleaning, or sanitation in a timely manner.
  • Review all documents in a timely fashion.
  • Conduct an annual management review meeting.
  • Maintain KPIs to monitor overall performance of High North Laboratories.
  • Manage and secure master copies of all methods and SOPs.
  • Manage and review temperature and humidity of all equipment and rooms, and handle excursions using scientific methods.
  • Perform other tasks as assigned by the CEO and President/COO.

About the Company

Eurofins

Global lab testing and analytics network

Eurofins provides global laboratory testing and analytical services to verify the safety, authenticity, and quality of products across food, water, medicine, and the environment. It operates a network of more than 900 laboratories in over 60 countries, offering access to more than 200,000 analytical methods. Its product work involves running specialized tests—using chemistry, biology, and other scientific techniques—to confirm origin, composition, and compliance of samples, such as detecting wine fraud or contaminant presence. The company differentiates itself through its massive, distributed lab network and broad portfolio, enabling standardized testing at scale and fast turnaround across many industries, rather than relying on a single specialty or location. Its goal is to protect public health and safety by delivering accurate, comprehensive testing data and helping clients meet regulatory and quality requirements.

Company size
10,001+
Company stage
IPO
Headquarters
Luxembourg
Founded
1987

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