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Alternate Quality Assurance Person

Job in Pickering, Ontario, C1V, Canada
Listing for: CannaPiece Corp.
Full Time position
Listed on 2026-08-29
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist, QA Specialist - Analyst/Manager
Salary/Wage Range or Industry Benchmark: 70000 - 80000 CAD Yearly CAD 70000.00 80000.00 YEAR
Job Description & How to Apply Below

Salary Range: $70,000.00 To $80,000.00 Annually

Duties & Responsibilities Regulatory Compliance & Product Quality
  • Support the QAP in fulfilling all statutory responsibilities under the Cannabis Act, Cannabis Regulations, and GPP/GMP.
  • Serve as the AQAP and assume QAP responsibilities, including product release decisions, when designated.
  • Review and approve batch production records, laboratory results, specifications, deviations, and quality documentation to ensure compliance prior to product release.
  • Ensure cannabis products are manufactured, packaged, labelled, tested, stored, and distributed in accordance with all applicable regulatory requirements and Company quality standards.
  • Maintain current knowledge of Health Canada guidance documents, regulatory changes, and industry best practices.
Quality Management System (QMS)
  • Maintain and continuously improve the Company'sQMS.
  • Develop, review, and approve SOPs, work instructions, forms, specifications, and controlled documentation.
  • Lead or support investigations involving deviations, non-conformances, complaints, out-of-specification results, root cause analyses, CAPAs, change controls, and risk assessments.
  • Monitor quality trends and recommend improvements that strengthen compliance, product quality, operational efficiency, and customer satisfaction.
  • Ensure quality records are complete, accurate, and maintained in accordance with regulatory retention requirements.
Audits, Inspections, & Continuous Improvement
  • Lead or participate in internal audits, supplier qualification activities, customer audits, and Health Canada inspections.
  • Coordinate responses to audit observations and inspection findings, ensuring timely implementation of corrective actions.
  • Partner with operational departments to identify opportunities for continuous improvement while maintaining regulatory compliance.
  • Participate in validation activities, process improvements, new product commercialization, and change management initiatives.
  • Provide quality leadership and technical guidance to employees across the organization.
  • Deliver GPP/GMP-and quality-related training while promoting a culture of compliance, accountability, and continuous improvement.
  • Build collaborative relationships with Production, Extraction, Packaging, Maintenance, Engineering, Commercial, and Supply Chain teams.
  • Support the development of quality metrics and Key Performance Indicators (KPIs) to measure and improve organizational performance.
  • Act as a trusted advisor to management on quality and regulatory matters.
Other
  • Perform other duties and responsibilities as assigned.
Qualifications Education
  • Bachelor's degree or diploma in Chemistry, Microbiology, Biology, Pharmaceutical Sciences, Food Science, Engineering, or another relevant scientific discipline.
Experience
  • Previous experience as a QAP or AQAP within a Health Canada-licensed cannabis facility is strongly preferred.
  • Demonstrated experience within a GPP or GMP regulated manufacturing environment.
  • Experience supporting Health Canada inspections and regulatory compliance activities.
  • Experience maintaining a QMS within a regulated industry.
  • Experience leading investigations, CAPAs, change controls, and quality risk assessments.
  • Previous leadership or supervisory experience is considered an asset.
Knowledge & Technical Skills
  • Thorough knowledge of the Cannabis Act, Cannabis Regulations, GPP/GMP, and applicable Health Canada guidance.
  • Strong understanding of Quality Management Systems, document control, investigations, risk management, CAPAs, complaints, change management, and internal auditing.
  • Experience reviewing and approving batch documentation and quality records.
  • Strong technical writing skills with experience developing SOPs, specifications, investigations, and regulatory documentation.
  • Proficiency with Microsoft Office, ERP systems, QMS platforms, Adobe Acrobat, Smart Sheets , and electronic document management systems.
  • Ability to analyze data, identify trends, and make sound, risk-based decisions.
  • Excellent judgment and the confidence to make independent quality decisions.
  • Strong integrity and commitment to regulatory compliance.
  • Exceptional organizational skills with the ability to…
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