Process Engineer

EFOR; Galway; On-site; EUR 60,000 - 90,000; Full time

Job summary

EFOR Group in Galway, Ireland, is seeking a Technical Services Engineer to optimize sterile pharmaceutical manufacturing processes and lead technology transfer for new product introductions. The role involves cross-functional collaboration with Production, Quality, Regulatory and Engineering to ensure compliant scale-up and commercialization.

Ideal candidates will have 3–7 years in pharmaceutical manufacturing, hands-on aseptic and lyophilization experience, and strong knowledge of cGMP, FDA/EMA

Qualifications

• Bachelor’s or Master’s degree in Chemical/Pharma/Biotech Engineering or 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.
• Knowledge of cGMP, Annex 1, FDA, EMA, ICH and validation/qualification protocols.
• Hands-on experience with aseptic technology, lyophilization, risk assessments and process equipment.

Responsibilities

• Develop, optimize, and validate sterile pharmaceutical manufacturing processes.
• Drive technology transfer, alternate source qualification, and new product introductions.
• Support production teams with troubleshooting across manufacturing phases.
• Perform risk assessments, lead root cause investigations, and implement improvements.
• Collaborate with Production, Quality, Regulatory and Engineering to scale-up and commercialize processes.

Skills

Process engineering

Aseptic manufacturing

Cross-functional collaboration

Regulatory compliance

Lean/Six Sigma

Automation systems

Education

Bachelor’s or Master’s in Chemical/Pharma/Biotech Engineering or related field

Tools

SCADA

MES

PAT

FMEA

Job description

Now Hiring: Technical Services Engineer – Product & Process (Galway, Ireland | Onsite)

Are you an expert in aseptic pharmaceutical manufacturing, eager to optimize processes and drive new product introductions? EFOR Group, a trusted Life Sciences consulting partner, is seeking a skilled Process Engineer to join our team in galway.

What you’ll do:

• Develop, optimize, 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 commercialization

Your background:

• Bachelor’s or Master’s in Chemical/Pharma/Biotech Engineering or 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, lyophilization, 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: Galway, Ireland (onsite)