Today, Lonza is a global leader in life sciences operating across five 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. This is a fully site‑based role. Working together in person supports close, real‑time collaboration
The actual location of this job is in Basel, Switzerland. The Global Transformation Lead for Indirect Procurement acts as a strategic member for the Global Indirect Procurement organization, reporting directly to the Head of Global Indirect
Location: the actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. The Contamination Prevention & Control (CPC) Environmental Monitoring (EM) team delivers critical GMP
The actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. As a Supplies and Inventory Manager (m/f/d) at our Visp site, you play a
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 dedicated people working together,
Engineering Planner (m/f/d) Freelance/Contracting project Visp Start date: asap Reference number: /1 Diesen Job teilen oder drucken Responsibilities Maintenance scheduling - Develop and maintain maintenance and calibration schedules for all plannable activities, including planned and unplanned tasks
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 represent Quality Assurance in cross-functional teams, establish and maintain interfaces with
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