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 youABOUT 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 technologiesChromatography ColumnsClean-in-place (CIP) and steam-in-place (SIP) systemsWFI, clean steam, and process gasesProcess tanks, skids, and associated pipingConduct 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 equipmentUtility 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 applyApply via this advert or contact Cian Marnane on if you have any more questions about this role