Validation Engineer
We are seeking a skilled professional to ensure the ongoing validation compliance of computerised equipment and systems in a sterile manufacturing environment.
Key Responsibilities:
* Lead and support validation activities for new and existing computerised equipment and control systems.
* Generate validation documentation (protocols/reports) and assist with the execution of validation protocols.
* Participate in the change control process, advising on CSV matters.
* Contribute to the development and execution of DQ, IQ, OQ, and PQ protocols.
Maintaining validation documentation and ensuring equipment and systems remain compliant with current Good Manufacturing Practice requirements is crucial. Support preparation, review, and approval of validation/revalidation plans and site change controls will also be required.
Our ideal candidate has a strong technical knowledge of pharmaceutical operations and experience in a healthcare manufacturing environment, ideally within the pharmaceutical sector. Familiarity with GAMP, ISPE Baseline Guides, and quality/compliance regulations is essential.
This role requires excellent communication skills, attention to detail, and the ability to work independently and collaboratively as part of a team.
The successful candidate will have the opportunity to develop their skills and knowledge in a dynamic and challenging environment.
We are an equal opportunities employer and welcome applications from all qualified candidates.