CQ Engineer

EFOR

Geel

On-site

EUR 70,000 - 90,000

Full time

14 days+

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Job summary

EFOR Group, a trusted Life Sciences consulting partner, is seeking a Commissioning & Qualification Engineer to support a world-leading pharmaceutical company at its Geel API manufacturing site. The role focuses on leading the qualification of complex process equipment and utilities in a GMP environment.

You’ll collaborate with Engineering, Automation, Production and QA to ensure clean handovers, maintain regulatory compliance, and contribute to continuous manufacturing initiatives and the site’s

Qualifications

  • 3+ years’ C&Q experience in GMP pharmaceutical, API or fine chemicals environment.
  • Hands-on qualification of chemical process equipment (reactors, dryers, centrifuges, containment systems).
  • Solid knowledge of cGMP (EU GMP Part II / ICH Q7), Annex 15, GAMP 5 and risk-based qualification.
  • Experience with high-potency (HPAPI) containment, ATEX zones or solvent handling is a strong advantage.
  • Familiarity with paperless validation tools (e.g. Kneat), DCS/PLC automation (DeltaV, Siemens) or continuous manufacturing is a plus.
  • Fluent English; Dutch is a real asset.

Responsibilities

  • Lead commissioning and qualification of API process equipment and systems: reactors, centrifuges/filter-dryers, vacuum dryers, mills, isolators and glove boxes
  • Qualify supporting utilities and infrastructure, including HVAC, purified water, nitrogen, process piping and solvent systems
  • Write and execute C&Q deliverables (URS, system impact and risk assessments, FAT/SAT, commissioning protocols, IQ/OQ/PQ) following ASTM E2500 and a risk-based approach
  • Manage discrepancies, deviations and change controls during execution, working closely with vendors, Engineering, Automation, Production and QA
  • Support capital projects linked to the site’s move towards continuous manufacturing, digitalisation and its carbon‑neutral 2030 roadmap
  • Make sure systems are handed over qualified, documented and inspection‑ready

Skills

C&Q experience
GMP knowledge
DCS/PLC automation
HPAPI containment
Kneat validation
Fluent English
Dutch language

Education

Bachelor’s or Master’s in Chemical/Mechanical/Process/Industrial Engineering

Tools

DeltaV
Siemens
Kneat

Job description

Does qualifying a high-containment reactor train sound more exciting than another cleanroom? EFOR Group, a trusted Life Sciences consulting partner, is looking for a Commissioning & Qualification Engineer to support a world-leading pharmaceutical company at its large-scale Active Pharmaceutical Ingredient (API) manufacturing site in Geel, where chemistry, high-potency handling and digital innovation meet.

What you’ll do:
  • Lead commissioning and qualification of API process equipment and systems: reactors, centrifuges/filter-dryers, vacuum dryers, mills, isolators and glove boxes
  • Qualify supporting utilities and infrastructure, including HVAC, purified water, nitrogen, process piping and solvent systems
  • Write and execute C&Q deliverables (URS, system impact and risk assessments, FAT/SAT, commissioning protocols, IQ/OQ/PQ) following ASTM E2500 and a risk-based approach
  • Manage discrepancies, deviations and change controls during execution, working closely with vendors, Engineering, Automation, Production and QA
  • Support capital projects linked to the site’s move towards continuous manufacturing, digitalisation and its carbon‑neutral 2030 roadmap
  • Make sure systems are handed over qualified, documented and inspection‑ready
Your background:
  • Bachelor’s or Master’s in Chemical, Mechanical, Process or Industrial Engineering, or a related field
  • 3+ years’ C&Q experience in a GMP pharmaceutical, API or fine chemicals environment
  • Hands‑on qualification of chemical process equipment (reactors, dryers, centrifuges, containment systems)
  • Solid knowledge of cGMP (EU GMP Part II / ICH Q7), Annex 15, GAMP 5 and risk-based qualification
  • Experience with high‑potency (HPAPI) containment, ATEX zones or solvent handling is a strong advantage
  • Familiarity with paperless validation tools (e.g. Kneat), DCS/PLC automation (DeltaV, Siemens) or continuous manufacturing is a plus
  • Fluent English; Dutch is a real asset
Why EFOR Group?

EFOR brings together more than 3,200 experts in 18 countries, delivering technical, quality and engineering excellence across the full Life Sciences product lifecycle. Join a team helping to make the medicines of tomorrow, more safely and more sustainably.

Ready to qualify the chemistry behind life‑changing medicines?
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