Lead API C&Q Engineer for Large-Scale Pharma Projects

Dillon Engineering Services

Munster

On-site

EUR 110,000 - 138,000

Full time

4 days ago
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Job summary

Dillon Engineering Services is seeking an experienced Senior Process C&Q Engineer / CQV API Project Lead for a contract in Tipperary, Ireland. The role focuses on commissioning and qualification of API process equipment and utilities, from construction handover through start‑up and final handover.

The ideal candidate will have extensive C&Q experience in pharma/API environments, with hands‑on knowledge of Filter Dryers and ANFDs, and a strong track record supporting GMP/QA requirements.

Qualifications

  • Minimum 10 years' experience in Commissioning & Qualification (C&Q/CQV).
  • Experience with API process equipment and pharmaceutical utilities.
  • Experience leading C&Q activities on large pharmaceutical projects.
  • Knowledge of GMP, GEP and regulatory requirements.

Responsibilities

  • Prepare, review and execute commissioning and qualification documentation for API equipment and utilities.
  • Develop and execute IOC/IOQ protocols and installation verification.
  • Lead field walkdowns, start‑up, and qualification activities.
  • Coordinate contractors and vendors for commissioning tasks.
  • Ensure safety, compliance and smooth project handover.
  • Provide technical guidance to C&Q personnel.

Skills

C&Q experience
API equipment
Project leadership
GMP/GEP knowledge
Document control
Troubleshooting
Communication skills

Education

Engineering or science degree

Job description

Dillon Engineering Services is seeking an experienced Senior Process C&Q Engineer / CQV API Project Lead for a contract in Tipperary, Ireland. The role focuses on commissioning and qualification of API process equipment and utilities, from construction handover through start‑up and final handover.

The ideal candidate will have extensive C&Q experience in pharma/API environments, with hands‑on knowledge of Filter Dryers and ANFDs, and a strong track record supporting GMP/QA requirements.

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