The actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. As our operations continue to expand, we are looking for motivated MSAT Data Managers (m/f/d)
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 in
Location: the actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. What you will get: An agile career and dynamic working culture An inclusive
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
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,
The actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. The role involves interacting with many departments and managing various stakeholders at different levels.
Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together,
The actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. The Logistics Operation Lead BioLOG, together with the team leads, is responsible for the
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,