This global biopharmaceutical leader wants two ambitious, driven and experienced QA professionals to join their Quality department in their Cork branch.
Shift work may be required.
Supporting site quality systems, manufacturing operations and inspection readiness
Ensuring site preparation for GMP operations by supporting cross functional initiatives
Reviewing and approving electronic and paper production batch records
Releasing Raw Materials for production
Supporting Technology Transfer of a new product into the site including raw material and supplier qualification
Reviewing and approving Trackwise deviation and investigations reports
- Providing support as required: Document control, New or updates to relevant quality agreements, process and Cleaning Validation activates
- Bsc Degree in a technical discipline (science, physical, engineering, chemical or biological science, pharmacy)
- 3+ years relevant experience in a cGMP regulated manufacturing environment,
- Knowledge and proficiency in Quality Assurance and Compliance
For a confidential discussion on this or any other current job opportunity please contact Marcel Skolimowski on 021 4847 138 / email@example.com
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