DQA

Eurofins Advinus provides preclinical research, drug development, and contract manufacturing services. This role controls quality documents and systems, supports audits, reviews records and materials, and releases finished products.

• Revise, issue, withdraw, and archive controlled quality documents
• Maintain document master lists and issue forms and registers
• Review department SOPs, laboratory records, analytical reports, and specifications
• Handle vendor qualification, customer queries, and dispatch activities
• Support internal and customer audits and perform in-process quality rounds
• Review quality events and approve certificates, materials, and finished-product batches

Experience

5+ years

Domain

pharmaceutical research

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