Job Description
Job Overview
We are looking for a dedicated Batch Record Reviewer 80-100% (f/m/d) for our site in Visp.
Key Responsibilities
- Responsible for the planning, execution and documentation of manufacturing campaigns for drug product in compliance with cGMPs, SOPs and applicable guidelines.
- Secure that each batch is manufactured safely, on time and in compliance with batch instructions and quality requirements.
- Provide front‑line technical and procedural support while working with manufacturing teams (operators), plant engineers and QA operations.
- Establish, with high quality and on time, the required production documentation (preparation and review of electronic batch records) or other relevant GMP documents for the assigned production area.
- Lead process‑related investigations and critical deviations and assist in decision‑making on production issues.
- Lead process changes, CAPAs and CAPA effectiveness checks rel...
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Submit your application today and join our talented team at Lonza Group Ltd..
Submit ApplicationJob Details
- Location oberwallis, wallis
- Job Type Full-time
- Category IT & Technology
- Posted Date June 03, 2026
- Application Deadline July 13, 2026