About the job
Kerry | Contract | Hybrid
I'm currently working with a global pharmaceutical manufacturer that is expanding its state-of-the-art manufacturing facility in Kerry. We're looking for an experienced Lead CQV Engineer to take ownership of commissioning, qualification and validation activities for packaging and inspection systems as part of a major capital expansion.
Key Responsibilities
- Lead CQV activities for Bulk Packaging, Automated Visual Inspection (AVI) and Headspace Analysis equipment.
- Manage commissioning and qualification from FAT through to PPQ.
- Develop and review CQV documentation including IQ/OQ/PQ protocols and reports.
- Coordinate with Engineering, QA, Validation and Automation teams throughout project delivery.
- Support international FAT activities with equipment vendors.
Qualifications & Experience
- Degree qualified in Engineering, Science or a related discipline.
- Proven Lead CQV experience within pharmaceutical or biopharmaceutical manufacturing.
- Strong experience with Bulk Packaging, AVI and Headspace Analysis.
- Experience delivering CQV activities on GMP capital projects.
- Ability to travel internationally for FAT activities when required.
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