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Pharmaceutical Quality Assurance Supervisor

Young-Innovations

Lead pharmaceutical quality assurance through investigations, CAPAs, and QMS oversight at Germiphene Corporation’s Brantford manufacturing site. Apply structured problem-solving across regulated products.Reporting to the Quality Manager, this hands-on supervisor leads assigned QA staff and supports Drug GMP and ISO 13485 / MDSAP frameworks. The work covers deviations, OOS results, complaints, annual reviews, KPI trending, SOPs, and audit readiness. You will collaborate with Operations, QC, Regulatory Affairs, and R&D.Key Responsibilities:
Lead deviation, OOS, complaint, non-conformance, and CAPA investigationsApply Fishbone, 5 Whys, and FMEA root-cause toolsDrive CAPAs through effectiveness verification and closureAuthor, revise, and approve SOPs and formsSupervise workloads, coaching, reviews, and trainingRequirements:
University degree in a science disciplineMinimum five years’ pharmaceutical or medical-device quality experienceKnowledge of Health Canada Drug GMP and ISO 13485 / MDSAPExperience with electronic QMS and audit-trail reviewsStrong technical, regulatory, analytical, and statistical writing skillsUse investigations, CAPA leadership, KPI trending, and clear documentation to strengthen quality at Germiphene’s Brantford site.
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Vacancy posted 1 hour ago
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