Join Eurofins as a Biologics QA Associate, where your expertise in quality assurance will directly impact pharmaceutical safety. Gain hands-on experience in a state-of-the-art cleanroom environment.
In this key role, you will assist the QA Manager in maintaining compliance with cGMP across various Biologics operations, including fill-finish capabilities and analytical testing. Your insights will help guide quality systems improvements and support audit preparations while ensuring product integrity and safety.
Key Responsibilities:
• Oversee GMP activities in the Biologics unit
• Conduct reviews of batch records and compliance tests
• Support quality control lab data reviews and approvals




• Contribute to investigations and corrective actions
• Aid in audit support and preparation processes
Requirements:
• Bachelor’s degree in Biochemistry or Microbiology preferred
• 2-5 years of related experience in QA
• Thorough understanding of cGMP practices
• Experience with monoclonal antibodies and therapeutic proteins
• Solid communication and interpersonal skills
Become a vital part of Eurofins and help enhance the safety of medicines through rigorous quality assurance practices.
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📌 Biologics QA Associate Role at Eurofins (Mississauga)
🏢 Eurofins
📍 Mississauga