QA Documentation Specialist / Batch Record Reviewer (7067)
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.