CQV Lead

CV-LibrarySevenoaks, KentcontractPosted: 1 May 2026
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We are currently recruiting for a CQV Lead to support a client outside of London.

Scope of Work:

* Day to day operations of the Validation Team ensuring all activities are appropriately planned, prioritised and executed

* Responsible for coordinating and supporting all validation activities, completed accurately, efficiently and within agreed timelines

* Collaboration with Engineering, Quality Assurance

* Coordination and execution of validation activities for all facilities, equipment and processes to ensure compliance with GMP

* Development, execution and completion of validation documentation including preparation of validation protocols, execution of validation activities and generation of final validation reports

Qualifications:

* BSc in Engineering, Science or equivalent

* Experience within CQV at Lead or Managerial level

* Previous pharmaceutical industry experience

* Experience with bioreactors, SIPs, CIPs, homogenisers, disk stack centrifuges

* Cleaning validation experience

* Grade A isolator and media fill (APS)

Start asap

Onsite 4 days

Outside IR35

6 months

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