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CQV Engineer

Job in 9700, Groningen, Groningen, Netherlands
Listing for: Panda International
Seasonal/Temporary position
Listed on 2026-08-06
Job specializations:
  • Pharmaceutical
    Validation Engineer, Quality Engineering, Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 85000 - 110000 EUR Yearly EUR 85000.00 110000.00 YEAR
Job Description & How to Apply Below
Overview   CQV Engineer (Utilities / USP-DSP) Sector:
Biologics / Pharmaceutical Manufacturing (GMP) Employment:
Temporary contract, 1 year

Location:

Onsite, 5 days/week Start:
October 2026 Experience

Required:

6+ years relevant experience

Education:

Chemical/Engineering, Biotechnology, or Pharmaceutical Engineering background MUST HAVE Proven track record independently driving, owning, and closing out multiple full CQV projects, covering commissioning, qualification, validation lifecycle, IQ/OQ/PQ execution, protocol writing/review, validation reports, and close-out. Scope in EITHER:
Utilities: WFI, clean steam, HVAC, clean gases, purified water, process utilities OR USP/DSP equipment: bioreactors, single-use systems, media prep, seed trains, cell culture (upstream) / chromatography, TFF, filtration, purification (downstream) Strong GMP Quality Systems ownership - Track Wise change controls, deviations, CAPAs, risk assessments, investigation support. Excellent project management skills, from kickoff through close-out.

Experience with GMP requirements and FDA/EMA regulations, particularly in biologics. Strong presentation and communication skills, including presenting to senior leadership. Good written and spoken English (Dutch a bonus).
WHAT YOU'LL ACTUALLY BE DOING   Owning full CQV project life cycles end-to-end, independently. Leading meetings and presenting progress/status to senior stakeholders. Managing Track Wise change controls and deviations to a high quality standard. Working under high-stress conditions and tight deadlines. Operating with autonomy onsite, five days a week.
WORK STYLE THAT FITS   Genuinely independent operator - comfortable owning a project without heavy oversight. Resilient under deadline pressure and high-stakes GMP environments. Confident communicator at senior/leadership level, not just peer-to-peer. Detail-oriented but able to see the bigger quality/compliance picture, not just execute steps.
STRONGLY PREFERRED BACKGROUND   Biologics manufacturing experience - mammalian cell culture, biotech facilities, large molecule production.

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