LSC have a great contract opportunity for a Junior CQV Engineer (Utilities) 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 2 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: Generating and completing CQV documentation to satisfy requirements and executing test deliverables for requalification and periodic review testing as applicable. Adhering to deadlines as scheduled by the team leader. Inputting to a wider CQV team and liaising with cross-functional teams to ensure timely completion and approval of CQV deliverables. Investigation support using QMS (Quality Management Systems) and troubleshooting for CQV issues. Ensuring adherence to governing site and global procedures and regulatory guidelines. ABOUT YOU - ARE YOUR SKILLS A MATCH? The candidate should hold a minimum of a BS qualification (Degree) in a scientific, technical, or engineering discipline. Previous CQV experience is an advantage, previous GMP experience is essential. The ideal candidate would have biopharmaceutical Process / Validation knowledge. 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: Commissioning Qualification Validation