Role OverviewWe are looking for an experienced Commissioning, Qualification & Validation (CQV) Engineer to support validation activities within a highly regulated pharmaceutical manufacturing environment.In this role, you will contribute to the commissioning, qualification, and validation of equipment, systems, and facilities, ensuring compliance with cGMP requirements and industry regulations.You will collaborate closely with engineering, quality, and

For our client, a global leader in the life sciences industry based in Visp, we are looking for a highly experienced CQV Engineer. The CQV Engineer is a critical role responsible for the commissioning, qualification, and validation of equipment and facilities. This role ensures that all installations meet stringent regulatory and technical standards, coordinating across departments to move projects from installation to full GMP compliance. General

Location: Switzerland (100% on-site)Contract type: Full-timeLanguage: German (mandatory); English a strong plusThe roleJoin a growing pharmaceutical site as a CQV Engineer owning validation activities for equipment, systems and facilities. You’ll coordinate installations, author and execute IQ/OQ/PQ protocols, and deliver audit-ready documentation in line with cGMP/GxP and internal procedures.What you’ll doPlan and coordinate CQV for facilities &