This is an exciting opportunity for an experienced to join our client, a leading Life Science company based in their new manufacturing facility in .
1. The development and maintenance of Quality System procedures.
2. Investigate/troubleshoot validation problems for components, equipment, and/or performance processes.
3. Monitoring and maintaining the quality and compliance status of associated quality records.
4. Writes, reviews, approves, and/or executes documentation for new and current validation procedures and technical reports related to components, equipment, products, and/or processes.
5. May assist with establishing corporate validation policies.
6. Maintaining the quality and compliance status of associated Procedures, work instructions, and training materials.
7. Presenting and communicating status, reporting metrics, identifying trends, potential issues, and improvement initiatives, as applicable.
8. Basic understanding of design controls and design transfer.
9. May be responsible for creating or participating in risk analyses and FMEAs.
10. Minimum 2 years experience in a similar industry
11. Minimum Level 7 NFQ qualification or equivalent in a relevant discipline