On behalf of our client, we are seeking an experienced Computer System Validation Engineer (P2) to support the qualification, validation, and lifecycle management of analytical laboratory instruments and computerised systems within a GMP-regulated environment.
📍 Location: Schachen (LU) / Onsite
📅 Start: 01 May 2026
⭐️ Workload: 100%
📄 Contract: Until 31 October 2026, with an option to extend
Key Responsibilities
Coordinate and execute equipment and instrument qualifications, including procurement, validation, upgrades, maintenance, and decommissioning.
Perform SDLC validation in collaboration with IT and site Validation teams.
Ensure timely calibration and metrology activities together with LAMP coordinators.
Support site-wide initiatives and projects related to Metrology & Validation and AR&D.
Review and assess alarms from controlled-temperature units such as stability chambers.
Provide initial troubleshooting for analytical laboratory instruments (e.g. HPLC, qPCR, plate readers).
Author and maintain SOPs, Change Controls, Periodic Reviews, and support deviation investigations.
Communicate daily with laboratory teams and managers to track progress and align on priorities.
Your Profile
Education (one of the following)
Technical apprenticeship in biotech, pharmaceutical industry, IT, or related fields.
Technical training in industrial equipment maintenance or management.
University degree in analytical chemistry, biotechnology, biochemistry, or an equivalent field.
Required Experience & Skills