Posted: 15h ago
The role
What you’ll do:
Develop, optimise, and validate robust pharmaceutical manufacturing processes for sterile products, ensuring regulatory compliance and operational excellence
Drive technology transfer, alternate source qualification, and successful new product introductions (NPI)
Support production teams with troubleshooting and resolving complex process challenges across all manufacturing phases
Perform risk assessments (FMEA), lead root‑cause investigations for deviations, and implement continuous improvement initiatives
Collaborate cross‑functionally with Production, Quality, Regulatory, and Engineering to ensure seamless process scale‑up and commercialisation
Your background:
Bachelor’s or Master’s in Chemical/Pharma/Biotech Engineering or a related field
3–7 years’ experience in pharmaceutical manufacturing, process engineering, or technical services
At least two years’ experience in sterile injectables or biologics manufacturing
Detailed knowledge of cGMP, Annex 1, FDA, EMA, ICH, and validation/qualification protocols (PPQ, CPV)
Hands‑on experience with aseptic technology, lyophilisation, risk assessments, and process equipment (filling, isolators, autoclaves, etc.)
Strong analytical mindset, excellent communication, and proven ability to work in cross‑functional teams
Lean/Six Sigma certification, experience with automation systems (SCADA, MES), or PAT is an advantage
Why EFOR Group?
EFOR unites over 3,200 experts in 18 countries, delivering unparalleled technical, quality, and engineering excellence across the full Life Sciences product lifecycle. Join a high‑performing team committed to healthcare innovation, safety, and reliability.
Location:
Inverin, Co. Galway, Ireland (onsite)
Ready to engineer the next generation of healthcare solutions?
Apply now or get in touch – interviews ongoing!
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