Commissioning and Qualification Engineer

Commissioning & Qualification Engineer (m/f/d) Ready to ensure quality and compliance in cutting-edge biopharmaceutical development? Duration: 09.01.2026 to 31.07.2026 Location: Schachen (Lucerne) Employment Type: Temporary Position Salary: CHF 8900 monthly About Our Client For our client, a globally leading biopharmaceutical company specializing in the development and testing of innovative biological medicines, we are seeking a motivated Commissioning & Qualification Engineer (m/f/d). This state‑of‑the‑art research and development facility in the Lucerne region plays a crucial role in the global network, providing analytical services and manufacturing clinical trial drugs for worldwide studies while operating one of only three forensic laboratories globally. Your Responsibilities Oversee and execute equipment qualifications, validations, and system lifecycle management activities including procurement, maintenance, and decommissioning within GMP‑regulated analytical laboratories Conduct system validation activities following SDLC methodology in close collaboration with IT teams and site validation units Manage analytical metrology by coordinating calibration maintenance services with Laboratory Asset Management Program coordinators to meet documented schedules and ad‑hoc business requirements Coordinate cross‑functional teams to qualify new analytical instrumentation and laboratory equipment Monitor and evaluate alarms from controlled‑temperature units such as stability chambers and other critical lab equipment Develop and maintain SOPs, change controls, and periodic review documentation for equipment and instruments Support and author deviation investigations and contribute to site‑wide projects related to Metrology & Validation Your Profile Technical education (apprenticeship) in biotech, pharmaceutical industry, IT, or related fields, OR technical training in industrial equipment management and maintenance, OR university degree in analytical chemistry, biotechnology, biochemistry, or related disciplines Proven experience in Commissioning/Qualification and/or Computer System Validation (CSV) Strong communication skills in English (B1 level) and German (B2 level), both written and oral Excellent documentation abilities with meticulous attention to detail on technical documents Demonstrated capacity for independent work and collaborative problem‑solving within cross‑functional teams Ability to deliver on tight timelines in a dynamic, fast‑paced environment Experience with GMP laboratories and thorough understanding of GMP policies and procedures is advantageous Familiarity with controlled‑temperature units, incubators, Change Management principles, and Deviation/CAPA management is a plus What We Offer Nemensis AG is your specialized personnel recruiter in the Life Sciences sector, based in Basel Comprehensive consultation and support throughout the application process by our experienced consultants Access to an extensive client network and exciting opportunities in Northwestern Switzerland Fast and straightforward onboarding through individual guidance and advisory during the recruitment process At nemensis ag, we have already connected thousands of candidates with their dream jobs, giving them the opportunity to develop further or re‑enter the job market. What can we do for you and your career today? Get in touch with us Are you looking for a change of perspective, but this isn’t the right position for you? Then register with us – we’ll contact you for an introductory meeting to understand your wishes and needs and align ourselves accordingly. Branche: Pharma-Industrie Funktion: Ingenieurwesen/Planung Anstellungsart: Befristeter Vertrag #J-18808-Ljbffr