What are the responsibilities and job description for the Commissioning & Qualification Engineer position at Warman O’Brien?
Warman O'Brien are delighted to partner with a Leading Pharmaceutical Company seeking a team of Engineers to support on a long term 12 month extendable project.
We are looking for Commissioning and Qualification Engineers and 4 x Area Leads in following areas: Clean Utilities, HVAC, Project Manager & Scheduler, Process Equipment.
Key Responsibilities:
- Develop and execute commissioning protocols (FAT, SAT, IQ, OQ, PQ).
- Lead qualification of equipment, utilities, and facilities in GMP-regulated environments.
- Perform risk assessments and ensure compliance with regulatory standards (FDA, EMA, GAMP, ISPE).
- Review system documentation (P&IDs, wiring diagrams) and participate in system walkdowns.
- Collaborate with engineering, manufacturing, and quality teams to support installation and commissioning.
Required Skills & Experience:
- 5 years of C&Q experience in Pharmaceuticals, Biotech, or Medical Devices.
- Strong knowledge of GMP, FDA, EMA, ISPE, and GAMP regulatory requirements.
- Hands-on experience with HVAC, bioreactors, clean utilities, process gases, and environmental monitoring systems.
1099 Contracts
Competitive Hourly Rate
Full time onsite - 40 hours per week
Start Date - April/May 2025
If you would like to be considered, please apply now to arrange for a confidential discussion with one of our recruiters!
