Quality Assurance Specialist
Posted on Jan 29, 2019 by Anonymous
* You will act as the point of contact for Quality Systems and processes providing site support and feedback on Sterile Manufacturing activities on site.
* Perform review of documentation, investigations, reports and continuously improve procedures whilst ensuring compliance to cGMP standards.
* The ideal candidate will hold working experience in quality within a cGMP Pharmaceutical/Bio setting.
* Understanding cGMP / US and EU regulatory requirements.
* Previous experience in Sterile operations/manufacturing and particularly release of sterile products.
In order to apply for this opportunity please send your CV or call Craig Bridgland on (phone number removed)
STR Limited is acting as an Employment Agency in relation to this vacancy