Step into a pivotal role at a global CMO and help shape the future of healthcare manufacturing.
Proclinical is seeking a QA Batch Record Reviewer to oversee GMP batch documentation and ensure full compliance with regulatory and internal quality requirements. Strong attention to detail and the ability to work independently are essential. German fluency is mandatory; English is preferred.
Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.
Responsibilities:
- Review paper-based executed batch records within specified timeframes.
- Track, report, and monitor batch record reviews and other critical metrics to ensure timely batch release.
- Address observations by raising meetings with Operations teams promptly.
Key Skills and Requirements:
- Professional experience in GMP production environments, quality procedures, and SOP execution.
- Academic background in Pharmaceutical Technology, Biotechnology, Chemistry, Pharmacy, or equivalent scientific fields.
- Experience in batch record review is highly preferred.
- Strong communication skills.
- Business fluent German is mandatory; English proficiency is preferred.
- Must be able to work on-site in Visp, Switzerland (no remote work).
If you are having difficulty in applying or if you have any questions, please contact Emile De Beer at e.debeer@proclinical.com.
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.
Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.
By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - https://www.proclinical.com/privacy-policy.
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