QA Batch Record Reviewer

QA Batch Record Reviewer (M/F/D) 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 of the Executed Batch Records (e.g. production documentation review, raw data etc)Support batch release by ensuring the completeness of the documentation packageReview comments added to the Executed Batch Records, clarify with the operations team and evaluate with the responsible QA ManagerSupport the initiation of deviations and investigations for Batch Record review related observations Qualification:Academic degree OR relevant work experience in Biology/ Chemistry/ Biotechnology or other related fieldPrevious experience in GMP regulated pharmaceutical / API industry is an advantageAbility to identify non-compliance and gaps from quality standardsStructured, precise and well-organized working attitude; open-minded for new ideas and suggestions; agile, highly motivated and dynamic driveFluent English (written and verbal) is required, German language skills preferred Requirements: Start: 01.01.2025Duration: 9 monthsCapacity: 5 days per weekLocation: Visp, Switzerland (2 days remote possible)