QA Document Specialist m/f/d
This job offer is no longer available.
3930 Visp, Switzerland |
Temporary Employment
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.
Tasks:
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.
Skills:
Professional experience in GMP production environment, quality procedures and SOP execution and/or 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
Additional:
On-Site in Visp (no home office) - Paper based
Business fluent German is a MUST, English preferre
Reference number: 17771
Industry: Pharmaceutical Industry
Project start: ASAP
Duration: 31.12.2026
Employment type: Temporary Employment
Contact
Tünde Verebélyi