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• Receipt / Download / Accepting of cases from Document Exchange Tool or electronically (or any other source)
• Translation of all relevant European Non-English information from source documents to English (if required) and updating relevant fields in Standard Adverse Event (AE) form

QA MANAGER - DRUG PRODUCT CLINICAL MANUFACTURING (M/F/D) - QUALITY ASSURANCE / PHARMACEUTICAL / CGMP / SYNTHETIC MOLECULES / GMP AUDITS / SAP / VEEVA / GERMAN / ENGLISH PROJECT: For our client, a large pharmaceutical company based in Basel, we are looking for a QA Manager (m/f/d) Drug Product...

• Scientific lead and coordination of Critical Quality Attributes (CQA) evaluations and product characterization studies
• Representation of Analytical Science in the customer project teams, coordination of activities and implementation of the QbD strategy

• Lead and develop the Product Risk Management team
• Own and continuously improve the risk management process according to ISOwithin our product development framework
• Ensure high-quality risk analyses and maintain consistent, audit-ready risk management documentation