Join Eurofins CDMO Alphora as a QA Associate with an emphasis on Biologics, dedicated to maintaining high-quality standards in pharmaceutical manufacturing. This position is full time and crucial for GMP compliance.

You will report to the QA Manager, Biologics and be responsible for quality oversight for biotechnology-derived pharmaceuticals, such as mAbs and therapeutic proteins. Your role will include reviewing batch records and analytical data for compliance while collaborating with various departments to ensure safe product release.

Key Responsibilities:
• Ensure compliance in batch manufacturing and packaging processes
• Review analytical data for raw materials and finished products
• Assist in audits and inspections for regulatory compliance




• Collaborate in developing quality systems and procedures
• Conduct root cause analyses for deviations

Requirements:
• Bachelor’s degree in Biochemistry, Microbiology, or related discipline
• 2-5 years experience in pharmaceutical quality
• Strong grasp of cGMP regulations
• Experience with biologics preferred
• Excellent verbal and written communication skills

Be part of Eurofins as a QA Associate, making strides in the pharmaceutical landscape while developing your professional skills.
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📌 Eurofins QA Associate - Biologics Focus (Ontario)
🏢 Eurofins Canada BioPharma
📍 Ontario