Key Roles/Responsibilities:
1. Provide QA input to project activities including review and approval of change requests, specifications, Standard Operating Procedures, Manufacturing Procedures and Analytical Procedures.
2. Participate in quality related investigations, assist in the development and approval of effective CAPA in order to resolve production, audit and customer issues.
3. Identify and escalate any identified cGMP areas of concern.
4. Participate in validation activities including approval of protocols and reports for analytical methods, manufacturing processes, analytical / production / packaging equipment and cleaning procedures
5. Participate in the audits of suppliers, production and support functions as required.
6. Be involved in the preparation for MHRA/FDA and other regulatory body audits.
7. Review the relevant documentation relating to incoming raw materials and perform the disposition activities as required.
8. Reviewing manufacturing, laboratory and associated documentation prior to performing the relevant disposition of final products. Where potential issues exist, these are to be highlighted to the QA manager.
9. Act as the QA representative for the introduction of new products, being a key member of the multi-functional team including R&D, QC and manufacturing thus ensuring that all cGMP documents are appropriate and all cGMP requirements are satisfied.
Competencies:
10. Attention to detail
11. Good communication skills, both verbal and written
12. Good organisation skills
13. Ability to work effectively individually and as part of a team
14. Ability to analyse data and information to make considered decisions
15. The ability to identify root cause of problems to determine appropriate solutions
16. Ability to prioritise workload to ensure timelines are met
17. Ability to follow instruction accurately
18. Ability to escalate issues as appropriate