Overview We are currently recruiting for a CQV Lead to support a client outside of London.
Responsibilities 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 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