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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