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, documentation
Location: Visp What you will get: A key role shaping our Global Engineering Functions Collaboration with a dynamic team in an innovative environment. An agile career and dynamic working culture An inclusive and ethical workplace Compensation
About Us ten23 health is a human-centric and sustainable strategic partner of choice for the pharmaceutical industry and biotech start-ups for the development, manufacture, and testing of tomorrow’s medicines. We support our clients in developing differentiated,
Join our Mission to Protect Humankind! Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working
Relocation assistance is available for eligible candidates and their families, if needed. For IbexTM Solutions, our unique biological manufacturing and development concept in Visp, Switzerland, we are looking for a Laboratory Technician (m/f/d) in Visp in
Switzerland, Visp Relocation assistance is available for eligible candidates and their families, if needed. Join our Engineering team and help shape the future of performance, reliability, and sustainability at our Visp site. In this role as
For IbexTM Solutions, our unique biological manufacturing and development concept in Visp, Switzerland, we are looking for a Laboratory Technician (m/f/d) in Visp in our team in Mammalian Purification Development. In this role, you will work
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