Commissioning Engineer - CQV
Location: Dublin, Ireland (Onsite)
Contract Duration: 11 Months
Commissioning Engineer - CQV - Drive Excellence in Pharmaceutical Industry
Are you a CQV pro ready to make a real impact in sterile pharmaceutical manufacturing? Join our team and lead the commissioning, qualification, and validation of cutting-edge equipment and utilities that ensure the highest quality for life-saving medicines.
What You'll Do:
- Develop, execute, and review CQV documentation for clean utilities and sterile manufacturing equipment.
- Ensure all systems are GMP, EU & FDA compliant throughout commissioning and qualification.
- Plan, execute, and leverage FAT/SAT testing to support overall qualification.
- Identify, assess, and mitigate CQV risks, generating actionable plans to keep projects on track.
- Manage deviations and CAPAs for assigned equipment and utilities.
- Collaborate with cross-functional teams and contractors to deliver projects safely, on time, and within budget.
- Ensure training compliance and contribute to continuous improvement initiatives.
- Support the handover of qualified systems to operations, ensuring seamless integration into production.
What We're Looking For:
- BS in Scientific, Technical, or Engineering discipline (required).
- 5+ years in pharmaceutical CQV, ideally with sterile drug product lines.
- Expertise in High Purity Water, Clean Steam, and Gas systems.
- Experience with electronic validation platforms (ValGenesis, Kneat).
- Strong communication and teamwork skills in matrix environments.
Why Join Us:
- Work on state-of-the-art pharmaceutical projects impacting patients worldwide.
- Grow your career in a highly innovative, collaborative environment.
- Make a direct impact on healthcare quality and safety.
Take your CQV career to the next level - apply today!
