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
- Strong 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.
GMP Batch Review Coordinator in Richmond Hill employer: Apotex Inc.
Apotex Inc. is an exceptional employer that prioritizes employee growth and inclusivity, fostering a collaborative work culture in the heart of Toronto. With a commitment to innovation in healthcare, employees benefit from comprehensive training programs, competitive compensation, and the opportunity to contribute to meaningful projects that improve access to affordable medications across LATAM. Join us to be part of a dynamic team where your contributions are valued and your career can flourish.
