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CQ Engineer – Clean Utilities (m/w/d)

Unternehmen
Tech'Firm Information Systems Zürich AG
Ort
Stein AG
Datum
02.10.2025
Referenznummer
186844

Join Our Innovative Team

Are you a skilled professional passionate about delivering high-quality, compliant solutions in a state-of-the-art pharmaceutical production environment? We invite you to consider an exciting opportunity with us, where you can contribute to advanced clean utility systems in a dynamic project.

Your Role

In this pivotal position, you will be instrumental in the execution of Commissioning, Qualification & Verification (CQV) activities. You will take full ownership of assigned systems, overseeing processes from boundary definition through Design Qualification, Commissioning, Installation Qualification, Operational Qualification, and release to operations.

Main Responsibilities

  • Defining and approving system boundaries
  • Preparing, executing & approving Design Qualification (DQ), Installation Qualification (IQ), Operational Qualification (OQ)
  • Executing GMP risk assessments (GMP-RAs)
  • Coordinating and supervising vendors during testing and commissioning activities
  • Ensuring compliance with cGMP, regulatory frameworks, and project procedures
  • Managing documentation and reporting via platforms such as COMOS and KNEAT
  • Working closely with project, engineering, and operations teams for smooth handover to operations

What We’re Looking For

  • Degree in Life Sciences or Engineering (or equivalent experience)
  • 3+ years of experience in commissioning and qualification within pharma/biotech or related regulated industries
  • Strong knowledge of clean utility systems (e.g., WFI, Clean Steam, Compressed Air)
  • Experience with DeltaV (Emerson) and other control systems
  • Familiarity with COMOS / KNEAT
  • Solid understanding of cGMP and regulatory requirements
  • Strong problem-solving skills and ability to work with minimal supervision
  • Fluent in English (spoken & written); German is a plus
  • Willingness to work shifts if required by project phase

Nice to Have

  • Strong knowledge of commissioning & qualification methodology
  • Broad biopharmaceutical facility background
  • Able to start ASAP in Switzerland

Why Join Us?

At Techfirm Industrial Services, we combine engineering expertise with impactful industrial projects. This opportunity provides:

  • Exciting exposure to large-scale biopharma projects
  • The chance to contribute to systems critical to global healthcare manufacturing
  • A collaborative environment with engineering experts and project professionals
  • Competitive compensation and project benefits

If you are eager to take ownership of clean utility CQ activities and join an ambitious project team, we encourage you to reach out. We look forward to exploring how you can contribute to our success.

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