Coordinate cleaning validation and quality support at Apotex, collecting equipment samples and completing documentation for pharmaceutical manufacturing activities. Apply GMP requirements consistently.

This Coordinator supports validation, verification, and monitoring activities under Apotex procedures and GMP requirements. You will log samples in SAP, forward them to QC or Microbiology laboratories, and maintain accurate training records. The position also provides training to new Coordinators and supports reserve sample inspections.

Key Responsibilities:

- Coordinate equipment cleaning validation sampling
- Complete validation activity documentation
- Log samples into SAP and forward them
- Maintain accurate individual training records
- Provide training to current Coordinators

Requirements:

- Related diploma or university degree
- Minimum two years pharmaceutical quality or production experience
- Familiarity with GMP and quality requirements
- Working knowledge of SAP, LIMS, and Trackwise
- Ability to work individually and collaboratively

Use cleaning validation, sample management, and GMP capabilities to support reliable quality activities throughout Apotex pharmaceutical production.

📌 Cleaning Validation Quality Coordinator (Canada)
🏢 Apotex
📍 Canada