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Commissioning Engineer

Job in 6106, Werthenstein, Kanton Luzern, Switzerland
Listing for: K-Recruiting Life Sciences
Full Time position
Listed on 2026-01-01
Job specializations:
  • Engineering
    Biomedical Engineer, Quality Engineering, Pharma Engineer, Process Engineer
  • Quality Assurance - QA/QC
    Quality Engineering
Salary/Wage Range or Industry Benchmark: 80000 - 100000 CHF Yearly CHF 80000.00 100000.00 YEAR
Job Description & How to Apply Below
Location: Werthenstein

Direct message the job poster from K-Recruiting Life Sciences

We unite the people who make our world healthier by placing top experts with life sciences companies worldwide. Precise. Fast. Accurate.

Commissioning & Qualification Engineer (M/W/D)

Responsibilities
  • Coordinate and conduct equipment qualifications, validations, and lifecycle activities including purchasing, maintenance, and decommissioning of analytical instruments
  • Perform system validation (SDLC) in collaboration with IT and the site validation unit
  • Support calibration and maintenance of analytical equipment in alignment with the Laboratory Asset Management Program (LAMP)
  • Support site‑wide Metrology & Validation projects and AR&D initiatives
  • Author SOPs, change controls, periodic review documents, and support deviation investigations
  • Check and evaluate alarms of controlled‑temperature units (e.g., stability chambers) and lab equipment
  • Coordinate with cross‑functional teams to ensure timely delivery of qualification and validation activities
  • Work independently and collaboratively within a dynamic team while maintaining GMP compliance
Qualifications
  • Technical education (apprenticeship or degree) in biotechnology, pharmaceutical sciences, IT, or related fields
  • Strong communication skills in English (B1) and German (B2) – verbal and written
  • High attention to detail with strong documentation skills
  • Experience in Commissioning & Qualification (C&Q) and/or Computer System Validation (CSV)
  • Ability to take initiative, solve problems, and coordinate with cross‑functional teams
  • Experience with GMP laboratory environment, controlled‑temperature units, and analytical instrumentation is an advantage
  • Affinity for technical maintenance of equipment and IT‑related software
  • Experience with Change Management, Deviations, CAPA, auditing, and compliance is a plus
  • Proficient in Microsoft applications (MS Office)
Framework data

Start
: 12.01.2026

Duration
: 12 Months

Seniority level

Associate

Employment type

Full‑time

Job function

Engineering and Information Technology

Industries

Staffing and Recruiting

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