Experienced in QA in the Medical/Pharma product areas, involved in document control, writing SOPs, ordering lab tests and has gained a strong background in Good Distribution Practice and Good Manufacturing Practice.
- Release documentation for releasing drugs onto market
- Checking documentation, attention to detail
- Sending samples to labs as per sampling plans
- Working in traceability and performing walk about with operations
- Process review, creation of processes
- Working with a digital management system to track CAPA
- Revision of processes, links to work instruction visual aids, and overdue CAPA's.
- Approve and coordinate CAPA and do root cause analysis, specifically 8D CAPA, root causes, preventative actions and implementing changes.
- He has been involved in internal and supplier audits in addition, as well as sending out questionnaires out to suppliers who are overdue.
He is immediately available to interview and would have 1 months notice.