Process Validation Lead | Permanent | Wiltshire / Hampshire
A Bio-Pharmaceutical client of Blackfield Associates are looking to add a Process Validation Lead to join their validation department. The Process Validation Lead looks after the process validation function within the department which typically consists of a handful of validation specialists who are all operating at various levels. This is an exciting opportunity with a biopharmaceutical manufacturer of vaccines and offers a unique opportunity to anyone who is looking to either enter biologics or sterile manufacturing.
Responsibilities include but are not limited to:
- Leading Continued Process Verification activities including the generation of CPV plans and reporting.
- Maintain and review the Product Control Strategy for all products. Understand the functional relationships that link CMA/CPP/PP to CQA.
- Communicate information on current process data which may impact Process Validation
- Author and review Process Validation plans, protocols and reports ensuring compliance
The ideal candidate will be qualified to degree level or equivalent and come from a pharmaceutical background, this is the sort of opportunity that would suit a high level lead that is looking to bridge the gap from being a technical lead and a managing lead. having a strong technical PV background is more important than having any lead or sterile knowledge.
This role is commutable from both Hampshire and Wiltshire.
For any questions regarding this position please email (url removed) or call (phone number removed).
STR Limited is acting as an Employment Agency in relation to this vacancy