Technical Services Engineer

Quanta Consultancy Services Ltd; Galway; On-site; EUR 60,000 - 80,000; Full time

Job summary

Quanta Consultancy Services Ltd is seeking a Technical Services Engineer for a 6-month contract in Galway, Ireland, to support sterile pharmaceutical manufacturing operations and contribute to manufacturing process performance.

The role requires hands-on experience with sterile/aseptic processes, PPQ/CPV validation, and strong technical writing to develop protocols, reports and validation deliverables, with a focus on GMP compliance and process improvement.

Qualifications

• 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.

Responsibilities

• 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.

Skills

Sterile / aseptic pharma manufacturing

Process validation (PPQ/CPV)

Technical documentation writing

MSAT / process engineering

Job description

Technical Services Engineer- 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 Technical Services 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 aProcess 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