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...