Description
A pharmaceutical company based within the East Midlands area require the services of a Validation Engineer on an initial 12 month contract.The successful Validation Engineer will be responsible for ensuring that all manufacturing processes, equipment, cleaning, utilities/facilities, computer and analytical methods are fully validated to meet the expected and operational requirements and GMP regulatory requirements.
As a Validation Engineer your key responsibilities include-
- Preparing, writing and executing validation protocols.
- Implementing validation strategies based on current regulatory and pharmaceutical industry standards and quality expectations.
- 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.
- Background in engineering in the pharmaceutical industry Experience of writing validation documentation Experience of validation of blister packaging lines would be beneficial Experience of validating HVAC would be beneficial
The successful Validation Engineer will need to have had at least 3-5 years Validation experience within a Pharmaceutical or GMP environment.
If you would like further information on this role, or you would like to apply please contact Halima Khanom on or email me directly with your current CV