For our site in Visp we are looking for a dedicated Batch Record Reviewer 80 - 100% (f/m/d) to extend our team.

Key Responsibilities

• Responsible for the planning, the execution and documentation of manufacturing campaigns for Drug Product in compliance to cGMPs, SOPs and applicable guidelines.
• Securing each batch is manufactured safely, on time, in compliance with the batch instructions and quality requirements.
• Provides front line technical and procedural support, working with the manufacturing teams (operators), plant engineers and QA operations.
• Responsible to establish timely and with high quality 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 assists in decision making on production issues.
• Lead process changes, CAPAs, and CAPA effectivene...