Description
A Leading Biopharmaceutical manufacturing organisation has an immediate requirement for an experienced QA Validation Specialist. Working at one of their facilities in the Middle East as the QAV Specialists you will be required to review and approve validation documents and reports.Responsibilities to include:
* To review validation documents (GAP Analysis) and ensure they are adequate for IBM review.
* To perform any remediation activities
Skills/Experience required:
* Education: Degree in either engineering or science
* Extensive experience within a biopharmaceutical manufacturing environment
* Proven background in completing QA review of validation strategies and protocols
* Experience from a QA perspective of reviewing the following validation documents: cleaning validation; equipment validation reports
*Previous experience PAI
*Knowledge of IMB
This exciting and challenging opportunity would suit an experienced QAV Specialist who is looking for a short term overseas opportunity