Salary not disclosed
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Role overview
Job description
Are you an experienced CQV Engineer looking to join a dynamic project team delivering complex pharmaceutical or life sciences projects? We are seeking a driven and collaborative CQV professional to support commissioning, qualification and validation activities across a range of GMP regulated systems, facilities and equipment. This is an excellent opportunity to work on high impact projects in a fast paced and technically challenging environment. Key Responsibilities Execute Commissioning, Qualification and Validation (CQV) activities in line with project schedules and GMP requirements. Support commissioning, startup and qualification of equipment, utilities and process systems. Prepare, review and execute validation documentation including protocols, reports, and traceability matrices. Lead or participate in design reviews, FATs, SATs, commissioning, IQ, OQ and PQ activities. Manage qual
…About this listing
- Source: CAI's official careers site (via Lever) · last confirmed on the source 1 Nov 2026
- Posted 20 Jul 2026
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What they are looking for
Skills & requirements
Qualification
We are seeking a driven and collaborative CQV professional to support commissioning, qualification and validation activities across a range of GMP regulated systems, facilities and equipment; Key Responsibilities Execute Commissioning, Qualification and Validation (CQV) activities in line with project schedules and GMP requirements; Support commissioning, startup and qualification of equipment, utilities and process systems; Manage qualification documentation through the full CQV lifecycle
Department · Europe Life Sciences
Hiring company
CAI
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