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Apotex Inc.Posted 10/21/2026full-timeNorth York • CanadaMid-LevelSenior💰 CA$83,958 - CA$139,930 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in quality assurance and compliance within the pharmaceutical industry, with a strong focus on GMP, GLP, and SOP adherence. Proven ability to lead teams, manage investigations, and optimize quality systems while ensuring regulatory compliance.
Highest-signal resume keywords
GMP ComplianceQA/QC ExperienceTeam LeadershipRegulatory KnowledgeAnalytical Thinking
About the role
Key responsibilities & impact- Ensure quality products are manufactured and packaged and packaging component testing is completed according to GMP, GLP, and SOP requirements
- Oversee daily QAIP Department operations
- Assign work to Technicians and Document Reviewers
- Troubleshoot manufacturing, packaging, in-process, and component-testing issues and recommend solutions
- Identify non-conformances and guide Lead Investigators
- Initiate and approve investigations as required
- Perform OOS investigations to determine root causes and corrective actions
- Notify the Manager of critical or major non-conformances
- Evaluate physical defects and recommend product disposition
- Ensure completion of annual retain-sample inspection batch lists
- Initiate CCRs and assist with approval of testing bulletins, SOPs, MPaRs, and PPM Masters
- Ensure documents comply with compendial and regulatory requirements
- Train employees on SOPs and GMP and maintain training records
- Monitor group work quality and efficiency, coordinate projects, and generate reports
- Ensure compliance with GMP, GLP, SOP, and safety protocols
- Ensure department equipment is adequate and maintained
- Review and approve laboratory equipment calibration reports
- Review and optimize processes and SOPs
- Serve as Departmental IS Lead and coordinate employee IS requirements
- Monitor group and individual activity via the IP Secure database
- Approve and schedule attendance and vacations
- Ensure department coverage and generate overtime schedules
- Schedule and conduct departmental meetings
- Cover the Manager’s duties during their absence
- Lead performance conversations, support employee development, and reinforce performance expectations
- Build trust-based relationships and foster a high-performance, safe working environment
- Recruit and onboard employees
- Ensure direct reports follow compliance programs, policies, and procedures
- Perform other duties as assigned
Requirements
What you’ll need- Bachelor of Science Degree or College Diploma in related field
- Familiarity with overall pharmaceutical manufacturing and quality systems/processes
- Good knowledge of global GMPs and QA/QC systems associated with manufacturing human drug products
- Proven ability to lead and motivate teams
- Experience with GMP regulations, including Health Canada, FDA, and EU regulations, is an asset
- Detail oriented, accurate, with personal leadership and accountability
- Excellent organization skills and analytical thinking
- Excellent written and verbal English communication skills
- Proven ability to effectively problem solve and provide guidance to the team
- Excellent interpersonal skills and ability to work effectively in a team environment
- Ability to manage multiple priorities in a fast-paced, high-pressure environment
- Experience with Microsoft Office: Word, Excel, Access, and PowerPoint
- Experience with SAP is an asset
- 3–5 years of QA/QC experience in the pharmaceutical industry
Benefits
Comp & perks- Bonus programs based on position in the organization
- Pay-for-performance philosophy
- Comprehensive benefits
- Pension plan
- Learning and development opportunities
- Accommodation for applicants with disabilities during recruitment
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Quality AssuranceQuality ControlRoot Cause AnalysisDocument ReviewInvestigationsProcess OptimizationTraining and DevelopmentDefect EvaluationSOP DevelopmentBatch Inspection
Soft Skills
Interpersonal SkillsProblem SolvingOrganizational SkillsCommunication SkillsTeam Collaboration
Tools & Technologies
Microsoft OfficeSAPIP Secure Database
Industry Keywords
Pharmaceutical ManufacturingGMP RegulationsGLP StandardsHealth CanadaFDA RegulationsEU RegulationsQuality SystemsNon-Conformance ManagementPerformance ManagementTraining Records