CordenPharma is a leading full-service contract development and manufacturing organization (CDMO) of active pharmaceutical ingredients (APIs), excipients and pharmaceuticals Drug Products (DP) and packaging capabilities with > 2’800 employees across the world. Our services enable pharmaceutical and biotech companies to manufacture medicines with the ultimate goal of improving people’s lives.

Our network in Europe and the US offers flexible and specialized solutions across six technology platforms: Peptides, Oligonucleotides, Lipids & Carbohydrates; Injectables; Highly Potent & Oncology; and Small Molecules. We strive for excellence in supporting this network and are committed to providing the highest quality products for the well-being of patients.

As soon as possible, at Fribourg site, we are looking for a

• Ensuring compliance with data protection regulations
• Reviews executed batch records
• Prepares the documentation to be transmitted to the contact givers after batch release
• Gives assessment to the qualified person before batch disposition decision
• Observes all health, safety and environmental protection measures within their area of responsibility
• Complies with quality procedures bases on GxP standards, including active participation in hygiene and good documentary practices
• Providing support for upcoming QA activities 

• Bachelor of Science in relevant field (Pharmaceutical industry, Chemistry)
• 1-2 years experience in Pharma / CDMO a plus 
• Knowledge of applicable GxP and related guidelines
• Professional in French (both in oral and written communication)
• Professional in English (in written communication)
• Computer skills