Support pharmaceutical compliance at Grifols as a Documentation Specialist in Winnipeg, managing GMP records tied to plasma testing and operations.

This QA-focused position controls documentation and records that directly or indirectly affect product quality, donor suitability, donor safety, plasma testing, and warehouse operations. Reporting to the Quality Management System Manager, the Specialist maintains lifecycle documentation and supports compliant processes under Canadian regulations and cGMP requirements.

Key Responsibilities:

- Manage SOP, form, protocol, and report documentation
- Circulate change requests for approval and distribute revisions
- Monitor documentation lifecycle information and indicators
- Maintain accurate, available,



legible controlled records
- Compile viral marker data for PPTA reports

Requirements:

- Health-related sciences bachelor’s degree
- At least two years’ relevant industry experience
- Understanding of Health Canada, FDA, and EMA GMP regulations
- Organized time management in regulated environments
- Excellent oral and written communication skills

Use GMP documentation, regulatory knowledge, and organized execution to support Grifols’ plasma-related quality activities in Winnipeg.

📌 Pharmaceutical Compliance Documentation Specialist (Canada)
🏢 Grifols
📍 Canada