Job description
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
Extra information
- Status
- Open
- Education Level
- Secondary School
- Location
- Kent
- Type of Contract
- Full-time jobs
- Published at
- 06-05-2026
- Full UK/EU driving license preferred
- No
- Car Preferred
- No
- Must be eligible to work in the EU
- No
- Cover Letter Required
- No
- Languages
- English
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