Description
Responsibilites:- Manage quality assurance activities for the advancement of the business through application of advanced quality systems and concepts.
- Maintenance of the Annual Product Quality Review systems and procedures to ensure compliance to current requirements. Review of current reports and tracking of CAPA commitments resulting from these reports.
- Review and approval of batch release data acting as QP on the appropriate MI.
- Tracking and management of batch release KPI targets for Quality, EME.
Education and Experience:
- Educated to degree level in Pharmacy, Chemistry, Biology, or relevant discipline
- Have substantial experience on a site holding a current Manufacturers License or Manufacturers Import Authorisation. Sterile manufacturing experience is preferred.
- Experience auditing suppliers and third party contract manufacturers
This is a great opportunity for someone looking to progress their career within a growing, global organisation and in return you will be rewarded with a competitive remuneration package. If you are interested or know anyone who might be, apply via this advert or contact Sarah Irvine on .