CQV Engineer

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 Cian Marnane on if you have any more questions about this role! Skills : CQV Documentation Project Management