Job Description

Jobdescription
About the role

We’re looking for a CQV Engineer to drive the validation of equipment, systems, and facilities in a regulated pharmaceutical environment. You will coordinate installations, author and execute IQ/OQ/PQ protocols, and document results in compliance with cGMP/GxP requirements—ensuring our operations are safe, compliant, and inspection-ready.

What you’ll do

  • Plan and coordinate CQV activities for facilities & utilities (e.g., HVAC, cleanrooms, WFI, clean steam) and production equipment.

  • Author, review, and maintain validation deliverables: URS, DQ, FMEA, Risk Assessments, FAT, SAT, IQ, IOQ/OQ, PQ and final reports.

  • Execute IQ/OQ/PQ testing, collect and analyze data, and produce clear, audit-ready documentation.

  • Apply validation lifecycle principles; perform gap analyses and risk assessments; identify efficiencies and lessons learned.

  • Monitor regulatory expectations;...

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