Our leading pharmaceutical client is seeking a QA Associate to joing their team in Cork. This is an 11-month contract.
- Ensure site preparation for GMP operations by supporting cross functional initiatives
- Review and approve electronic and paper production batch records
- Release Raw Materials for production
- Support Technology Transfer of a new product into the site including raw material and supplier qualification
- Review and approve Trackwise deviation and investigations reports, ensuring root causes have been identified and corrective action implemented
- Provide support as required: Document control, New or updates to relevant quality agreements, process and Cleaning Validation activates
The successful candidate will have:
- Bsc of Science degree, or equivalent, in a technical discipline (physical, engineering, chemical or biological science, pharmacy)
- Minimum 3 years relevant experience in a cGMP regulated manufacturing environment, with exhibited knowledge and proficiency in Quality Assurance and Compliance
- Experience in supporting manufacturing operations, batch record review and deviation/CAPA is highly desirable
If you would like to discuss this role, reach out to Louise Whitty on 021 2359140 / firstname.lastname@example.org
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