Validation Specialist Job in Wales, Wales UK
Validation Specialist - Pharmaceuticals - Permanent - South Wales
Our client is a leading UK pharmaceutical services companies, established for over 30 years. Our client is experienced in providing integrated drug development, clinical trial supply and manufacturing services to the international healthcare industry. At present they are recruiting a Validation Specialist on a permanent basis to be based at their manufacturing facility in South Wales.
The job holder will be degree qualified in Chemistry, Pharmacy or Microbiology with previous experience Validation experience within the pharmaceutical industry. The job holder be experienced working in a GMP environment and will have experience of preparing, reviewing and approving VMP`s (Validation Master Plans) and Validation plans. Candidates will generate and execute protocols and reports including IQ, OQ, DQ and PQ protocols and SOP`s and will review and approve FAT`s and SAT`s. The job holder will be ulitmately responsible for managing multiple validation tasks and will communicate effectively with colleagues and members within other departments. The job holder must be driven to implement change and drive projects through to completion. Knowledge of GAMP and CSV is also desirable to the role.
Our client is offering an exciting opportunity with a competitive salary and benefits package. Interviews will be immediate for suitable candidates.