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QA Associate (Pharma)

Job description

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.

Job responsibilities:

  • 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

Job requirements:

  • 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 / marcel@sigmar.ie

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