Description
This is an immediate position with a leading Medical Device company.Objectives:
- To provide support to the Quality Systems Manager in the setup, maintenance and continuous improvement of the Quality System.
- To set up and maintain the complaints process.
- To manage the administration and tracking for applicable Quality Systems.
- To manage, monitor and continually improve the Internal Audit Programme
- To manage, monitor and continually improve the Supplier Quality Programme.
- Set up and maintenance of the Risk Management process
Responsibilities:
- Manage and support external audits
- Supplier Quality, including investigations, non-conformances, MRB, supplier audits, supplier qualifications, reporting, measuring and monitoring.
- Complaints Management, including investigations, Non conformance and CAPA management.
- Management review and quality planning
- Continuous Improvement projects
- Risk Management Process
- Site GMP training
- Change Management activities
- Global Gap analysis review
- Maintain good documentation practices for Work instructions, SOP's and Forms.
Experience:
- Minimum 5 years' experience in a regulated pharmaceutical/medical device environment
- Experience in Quality auditing and supplier auditing
- Experience in Database management an advantage
If you would like to apply for this position please contact Sarah Irvine on . We also offer £200 worth of vouchers for any successful referrals!