Beschreibung

QA Documentation Specialist / Batch Record Reviewer (German-speaking)

Our client, a global market leader in the production and process support of active pharmaceutical ingredients, both in the chemical and biotechnology sectors, is looking for a QA Documentation Specialist for a contract position till end of 2026 (with option for extension) in Valais area, Switzerland.

This is an on-site position.

Making sure the batch was made properly, according to procedure and regulatory requirements. Reviewers should have great attention to detail, be able to work independently, and have a thorough knowledge of the manufacturing process they are reviewing.

Main Responsibilities:

• Review paperbased executed batch records within the specified timeframe.


• Track, report and monitor batch record review and other relevant critical metrics to ensure on-time batch release.


• Raise meetings with Ops related observations in a timely manner.

Qualifications and Experience:

• Relevant working/residency permit or Swiss/EU-Citizenship required


• Professional experience in GMP production environment, quality procedures and SOP execution


• Bachelor’s/Master’s Degree or equivalent experience.


• Preferred area of study: Pharmaceutical Technology, Biotechnology, Chemistry, Pharmacy or equivalent scientific degree.


• Experience in batch record review is highly preferred.


• GMP experience (min. 2 years)


• Great communication skills


• Business fluent German is a MUST, English preferred

Would you like to learn more about CTC and the opportunity outlined? Please, get in contact with us: you may either use the 'apply now' button, or write an email to us, or reach out to us on the phone.