Contribute to quality assurance processes at Biologics Manufacturing Centre as a Quality Assurance Process Specialist. Ensure compliance and product integrity as you manage critical release activities. This temporary, 13-month assignment at BMC involves overseeing drug substances and process intermediates under strict compliance measures.

You will assess deviations, participate in investigations, and serve as a resource for stakeholders. A robust grounding in GMP regulations is essential to support the center's mission of enhancing Canada's biopharmaceutical capabilities. Key Responsibilities:

- Release various drug products and process intermediates
- Review certifications and batch documents for compliance
- Identify discrepancies affecting product quality
- Lead collaborative investigations and prepare reports
- Support stakeholders in quality assurance processes Requirements:
- Bachelor's degree in a relevant field
- Five years in a GMP-regulated pharmaceutical environment
- One year of finished product release experience
- Proficient in French communication
- Solid understanding of GMP guidelines and quality standards Join BMC in ensuring the highest quality standards in biomanufacturing processes.

📌 BMC Quality Assurance Process Specialist (Montreal)
🏢 Socket.dev
📍 Montreal