We’re expanding our team in Visp and are currently seeking a motivated Intern for QA Documentation Support (m/f/d). In this role, you’ll report directly to the QA Operations Group Leader and collaborate closely with cross-functional teams
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
Company Description Swiss Delivery Excellence: Transforming Life Science Consulting Worldwide. Fusion Consulting is a globally leading Business and IT boutique consultancy specialized in the Life Sciences industry, partnering with leading companies in pharma, healthcare, and animal
Location: The actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. The role: The Senior QA Specialist (f/m/d) for QA Projects specifies quality requirements
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
Turn supplier relationships into high-performing, reliable supply chain outcomes. Proclinical is seeking an Operational Buyer to join the Supply Chain team in Swtzerland, supporting Small Molecules operations. This role focuses on ensuring the reliability and efficiency
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
Join our team at Lonza in Visp, Switzerland as a CQV Engineer / Qualification & Validation Engineer (m/f/d). Work alongside an outstanding team dedicated to maintaining flawless operations and premier standards. This role provides an exciting
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