CK Group are recruiting for a Validation Manager on behalf of a growing and award winning Medical Device manufacturer to be based at their site in Hartlepool on a permanent basis.
The role:
- Take the lead on validation activities for the processes and software related to product design together with creation and execution of validation protocols
- Create a plan for necessary revalidation activities based on risk assessment for all equipment, processes, and software.
- Perform all activities according to current version ISO 13485 and FDA 21 CFR Part 820.
- Help to create risk analysis for new projects related to product development
- Create changes and validation strategy for products and processes
Education:
- Degree or equivalent in an Engineering, Science or Clinical subjects, experience in the Medical Device (MD) and or In-Vitro Diagnostics (IVD) industries in similar position.
- Strong knowledge of ISO 13485 and US FDA 21 CFR Part 820
Apply:
It is essential that applicants hold entitlement to work in the UK. Please quote job reference 55180 in all correspondence.
You must have the right to work in the UK. Learn more
- Agency: CK Group
- Reference: 55180
Website: CK Group
- Posted: 1st March 2023
- Expires: 29th March 2023
