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CordenPharma is one of the leading Contract Development and Manufacturing Organizations (CDMO) and develops and produces active pharmaceutical ingredients, medicines and associated packaging services on behalf of its customers as a “full-service” service provider. The group employs around 3,000 people.

Our network in Europe and the USA offers flexible and specialized solutions across five technology platforms: peptides, lipids & carbohydrates, injectables, highly potent active ingredients & oncology and small molecules. We strive for excellence in supporting this network and are committed to providing the highest quality products for the benefit of patients.

CordenPharma International (CPI) acts as the management company of the CordenPharma Group. In addition to the Executive Leadership Team, CPI has central functions such as Sales & Marketing, Legal, HR and Corporate Development, which work for the CordenPharma Group across locations and at an international level.

We are looking for one as soon as possible

• Fribourg
• ASAP
• Full-time
• Fixed-Term

• 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

Brandt, Raphael