Eurofins CDMO Alphora Inc. is seeking a QA Associate specializing in Biologics to support compliance with Valuable Manufacturing Practices (cGMP). Focus on quality oversight for biotechnology-derived pharmaceuticals with a key emphasis on safety and efficacy.
In this role, the QA Associate will report directly to the QA Manager, Biologics. You will ensure compliance within the Biologics operating unit, including job functions like batch review and release and supporting the development of quality systems. Strong knowledge in pharmaceutical quality practices is a must.
Key Responsibilities:
• Provide quality oversight for GMP activities
• Perform batch manufacturing and final product packaging oversight
• Support review of change controls and logbook activities
• Review batch records and release analytical data
• Collaborate in deviation investigations and audits
Requirements:
• BSc in Biochemistry, Microbiology, or related field
• 2-5 years of pharmaceutical quality experience
• Understanding of cGMP regulations
• Experience with biologic pharmaceuticals preferred
• Strong written, verbal, and interpersonal skills
Utilize your quality assurance expertise to maintain high standards in Biologics operations at Eurofins.
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