Sterile Pharma Process Engineer | PPQ/CPV & Tech Transfer

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

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.