LSC have a great contract opportunity for a CQV Engineer to join a Dublin based Biopharmaceutical company dedicated to discovering, developing, and delivering innovative medicines that can help patients overcome serious diseases and improve their quality of life.
If you have 5 years of experience working in the pharmaceutical or biotechnology industry and are ready for your next challenge, this could be the perfect opportunity for you!
ABOUT THE PROJECT - KEY RESPONSIBILITIES:
- Deliver end-to-end CQV lifecycle documentation: URS, DQs, FAT/SAT, IQ, OQ, and support for PQ where applicable.
- Perform equipment and system commissioning, including verification of installation, utilities integration, control functionality, and safety systems.
- Lead CQV efforts on systems including (but not limited to):
- Bioreactors and single-use technologies
- Chromatography Columns
- Clean-in-place (CIP) and steam-in-place (SIP) systems
- WFI, clean steam, and process gases
- Process tanks, skids, and associated piping - Conduct impact assessments, risk assessments (e.g. ASTM E2500), and define appropriate qualification strategies.
ABOUT YOU - ARE YOUR SKILLS A MATCH?
- Bachelor's degree in Engineering, Life Sciences, or related technical field.
- Minimum 5 years' CQV experience in a GMP-regulated drug substance or biologics manufacturing environment.
- Demonstrated hands-on experience with commissioning and qualification of:
- Large-scale bioprocess equipment
- Utility systems (WFI, HVAC, compressed gases, clean steam)
- Automation-integrated equipment (DeltaV)
Note: Are you currently eligible to work in Ireland? As this is a contract opportunity you will need to hold a Stamp 1G/Stamp 4 visa to apply!
Apply via this advert or contact Adam Murphy on +353214718214 if you have any more questions about this role!
