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