The Batch Record Review Intern supports the Quality Assurance team (QA OPS) by assisting in the review, verification, and organization of electronic GMP manufacturing documentation. This role provides hands‑on exposure to regulated industry practices, including data integrity,
MSAT Cleaning Validation Expert Duration: 01/07/2026 - 31/12/2026 (+ possibility of extension) Location: Visp, Switzerland (on-site) Key Responsibilities Lead and execute equipment cleaning validation activities , including authoring and reviewing validation protocols and reports for: COP (Clean‑Out‑of‑Place) CIP
Location: The actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. You will own defined parts of the site Contamination Control Strategy at one
The Batch Record Review Intern supports the Quality Assurance team (QA OPS) by assisting in the review, verification, and organization of electronic GMP manufacturing documentation. This role provides hands‑on exposure to regulated industry practices, including data integrity,