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 cooperative 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 setting
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
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📍 Montreal