Process Engineer

Quanta Consultancy Services Ltd; Galway; On-site; EUR 45,000 - 60,000; Full time

Job summary

Quanta Consultancy Services Ltd in Galway is seeking a Process Engineer (Technical Services) for a 6-month contract to support sterile manufacturing operations within a pharmaceutical facility.

You will develop, validate, and troubleshoot sterile processes, author validation documentation and support technology transfer and NPI activities across the site, while leading deviation investigations to ensure GMP compliance.

Qualifications

• Experience in sterile/aseptic pharmaceutical manufacturing.
• Hands-on process validation (PPQ/CPV) in GMP environments.
• Proven ability to write protocols, reports and technical docs.
• Experience in MSAT or technical services in pharma manufacturing.

Responsibilities

• Support development, optimisation, and troubleshooting of sterile pharmaceutical processes.
• Author and execute process validation documentation including PPQ/CPV protocols and reports.
• Support technology transfer and NPI activities across site.
• Lead deviation investigations and root cause analysis for GMP compliance.

Skills

Sterile manufacturing

Process validation

Technical documentation

GMP compliance

Job description

Process Engineer (Technical Services) - Ireland, Galway - 6 Month Contract

Are you looking for the opportunity to work alongside a global pharmaceutical organisation in Galway? Our esteemed client is looking for a Process Engineer to join their team in their existing manufacturing facility in Galway. The facility is a responsible for tablet manufacturing (OSD) and secondary packaging (blister packing and bottle primarily for tablets and capsules), and our client is looking for a Process Engineer to help maintain manufacturing operations.

What you'll do:

• Support the development, optimisation, and troubleshooting of sterile pharmaceutical manufacturing processes


• Author and execute process validation documentation including PPQ/CPV protocols and reports


• Support technology transfer and new product introduction (NPI) activities across site


• Lead deviation investigations and root cause analysis to ensure GMP compliance and process improvement

What you'll need:

• Proven experience in sterile / aseptic pharmaceutical manufacturing


• Hands on experience with process validation (PPQ/CPV) in a GMP environment


• Strong capability in writing protocols, reports, and technical documentation


• Extensive experience in process engineering, MSAT, or technical services within pharma manufacturing