Eurofins CDMO Alphora is hiring a QA Associate specialized in Biologics to ensure the highest quality in pharmaceutical manufacturing. This full time role emphasizes compliance with cGMP standards.
In this position, you will support the QA Manager to oversee quality at the Biologics unit, focusing on the development and commercialization of innovative biologic therapies. Key tasks include batch reviews, analytical data verification, and participation in audits. You'll have the opportunity to work in a collaborative environment dedicated to pharmaceutical excellence.
Key Responsibilities:
• Monitor GMP activities including batch manufacturing and fill-finish operations
• Validate analytical methods for accuracy and compliance
• Review and approve production cleaning study reports
• Develop investigation plans for deviations and CAPAs
• Contribute to quality system improvements and SOP documentation
Requirements:
• BSc in a relevant scientific discipline
• 2-5 years in pharmaceutical quality assurance
• Proficient understanding of cGMP
• Background in biologics and sterile processing preferred
• Strong attention to detail and project management skills
Elevate your career in quality assurance at Eurofins and make a positive impact on patient health.
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