| London Jobs |
| Manchester Jobs |
| Liverpool Jobs |
| Nottingham Jobs |
| Birmingham Jobs |
| Cambridge Jobs |
| Glasgow Jobs |
| Bristol Jobs |
| Wales Jobs |
| London Jobs |
| Manchester Jobs |
| Liverpool Jobs |
| Nottingham Jobs |
| Birmingham Jobs |
| Cambridge Jobs |
| Glasgow Jobs |
| Bristol Jobs |
| Wales Jobs |
| Oil & Gas Jobs |
| Banking Jobs |
| Construction Jobs |
| Top Management Jobs |
| IT - Software Jobs |
| Medical Healthcare Jobs |
| Purchase / Logistics Jobs |
| Sales |
| Ajax Jobs |
| Designing Jobs |
| ASP .NET Jobs |
| Java Jobs |
| MySQL Jobs |
| Sap hr Jobs |
| Software Testing Jobs |
| Html Jobs |
| Job Location | Lenton Lane Industrial Estate |
| Education | Not Mentioned |
| Salary | £32,000 - £45,000 per annum |
| Industry | Not Mentioned |
| Functional Area | Not Mentioned |
| Job Type | Permanent, full-time |
CK Science are recruiting for a Validation Manager with a background in GMP manufacturing and equipment validation, to join a leading UK based pharmaceutical contract manufacturing business on a permanent basis in Nottingham. The Company:Our client is contract manufacturing and formulation business providing services mainly to the pharmaceutical sector. Location:The role is based at their location in Nottingham, easily commutable from main transport links. Validation Manager Role:To ensure that the systems, equipment and processes remain fit for purpose and qualified/validated to current regulatory requirements & guidance. Additionally there is significant contribution to the troubleshooting of operational issues relating to the manufacture of pharmaceutical products. This comes with one direct report into this role.Responsibilities:- Ensure that all manufacturing systems, equipment and processes are fit for purpose.- Ensure that procedures for all manufacturing systems, equipment and processes are clearly documented.- Manage, support and mentor the validation technician.- Provide support and technical advice to help manage and problem-solve issues arising in the business.Your Background:- Degree qualified in Science degree or equivalent.- In-depth GMP knowledge, particularly relating to the manufacture of sterile products. A strong preference for experience in steam sterilisation would be advantageous.- Understanding of regulatory standards for pharmaceutical products (MHRA/EMA/ISO etc.).- Significant experience (5+ years) of performing validation activities in a pharmaceutical or clinical trial manufacturing environment.- Some level of supervisory experience.Benefits:On offer is a competitive salary, a company pension scheme (ratio of 2:1 employer: employee contribution), childcare vouchers, cycle to work schemes, flexible working, 25 days holiday plus bank holidays and more. Apply:For more information or to apply for this position, please contact Naynesh at CK Group on or email , quoting job ref 49035.It is essential that applicants hold entitlement to work in the UK.INDGEN