Salary not disclosed
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Role overview
Job description
We are seeking an experienced CQV Lead to drive qualification and validation activities for a broad range of laboratory and benchtop equipment within a GMP-regulated environment. This position offers the opportunity to lead critical qualification projects, work closely with Quality, Engineering, Validation, and Laboratory teams, and play a key role in supporting both operational excellence and regulatory compliance. The successful candidate will provide technical leadership across the full equipment lifecycle, from installation and qualification through ongoing compliance and continuous improvement initiatives. Key Responsibilities Lead commissioning, qualification, and validation activities for laboratory and benchtop equipment within GMP environments. Develop and execute qualification documentation, including IQ, OQ, PQ protocols and final reports. Support the introduction of new labor
…About this listing
- Source: CAI's official careers site (via Lever) · last confirmed on the source 1 Nov 2026
- Posted 6 Oct 2026
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What they are looking for
Skills & requirements
Qualification
We are seeking an experienced CQV Lead to drive qualification and validation activities for a broad range of laboratory and benchtop equipment within a GMP-regulated environment; This position offers the opportunity to lead critical qualification projects, work closely with Quality, Engineering, Validation, and Laboratory teams, and play a key role in supporting both operational excellence and regulatory compliance; The successful candidate will provide technical leadership across the full equipment lifecycle, from installation and qualification through ongoing compliance and continuous improvement initiatives; Key Responsibilities Lead commissioning, qualification, and validation activities for laboratory and benchtop equipment within GMP environments
Department · Europe Life Sciences
Hiring company
CAI
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