Description
QA validation consultant
A great opportunity for a QA validation consultant to join a world renowned pharmaceutical organisation based in Belgium has recently become available. The position offers a fantastic benefits package alongside the chance to work in a modern, dynamic working environment.
Role responsibilities:
-To write and implement some validation documentation (VP, VSR),
-To review and approve specific qualification and validation documentation (IQ, OQ, PQ, PV),
-To support the production & technical services teams in the implementation of the validation activities,
-To ensure the adequate management of validation deviation and CAPA identification,
-To write and approve periodic review reports for primary bulk equipment/process.
Successful candidates will have:
- Validation & QA experience in a biopharmaceutical industry
- Technical knowledge in bulk equipments
- Good knowledge of pharmaceutical environments
- At least 2 years of experience in production, validation or QA in a biopharmaceutical industry
This really is a fantastic, career enhancing opportunity and the position will not be open for long. If you are interested in applying please send your CV to Daniel
Furthermore if you know of anyone that could be suitable we offer a generous referral bonus of euro;400 for any referral that results in employment so feel free to put them in touch!