Advance GMP compliance at Apotex by reviewing batch documents, inspecting samples, and supporting quality systems across pharmaceutical production. Work across documented procedures.
As a Coordinator, you will review and approve sterile and non-sterile production records according to established priorities. You will report deviations, verify corrections, and maintain batch information in the QA Supply Database. The position also supports inspections, audits, and customer complaint investigations.
Key Responsibilities: Review and approve applicable production documents
Report deviations from procedures and acceptance criteria
Ensure batch document corrections are properly supported
Inspect in-process and investigational samples
Support production and packaging area audits
Requirements: Community college diploma or related university degree
At least two years pharmaceutical quality or production experience
Ability to follow written procedures
Robust organizational and time management skills
Ability to manage multiple priorities
Bring GMP knowledge, batch review expertise, and organized documentation practices to Apotex quality operations as Coordinator.