Description
The main focus of the role would be Process Validation along with Computer Systems including the writing and implementing of documentation.The successful Validation Engineer will be responsible for ensuring that all manufacturing processes, equipment, and CSV activities are in line with operational requirements and cGMP regulatory requirements.
As a Validation Engineer your key responsibilities include-
* Preparing and writing validation protocols and SOPs.
* Ensure validation is delivered on time and according to company standards.
* Maintenance of validation systems and ensuring all processes, equipment and validation services remain relevant to the cGMP standards.
Ensure a gap analysis is conducted and the relevant risks and challenges are identified and addressed, to support ongoing release, licence submission/renewal, and ensure the procedures are audit ready.
The successful candidate will need to have had 5 years Validation experience within a Pharmaceutical or Medical Device environment. This role will also require knowledge of GAMP4/5 or 21 CFR part 11.
This is an exciting opportunity with competitive hourly rates. If you would like to apply please contact Sarah Irvine on . We also offer £200 worth of vouchers for any successful referrals so if you know of anyone who may be looking please feel free to get in touch.