CQV Lead

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-