LSC have an exciting opportunity for CQV Engineer to support projects in a cutting-edge pharmaceutical company based in Co. Wicklow. As a CQV Engineer in the project group, you'll play a crucial role in shaping the future of pharmaceutical manufacturing. ABOUT THE ROLE? Lead commissioning and qualification activities for state-of-the-art process and packaging equipment, facilities, utilities, and computerized systems Develop, review, and approve cGMP documentation for equipment, facility, utility, and computerized systems validation Drive project success from design through commissioning and qualification phases Manage vendor relationships and ensure compliance with quality standards Spearhead change control initiatives and foster a culture of continuous improvement ARE YOUR SKILLS A MATCH? Bachelor's degree in Engineering, Science, or a related technical field (engineering degree preferred) Minimum 5 years of experience in pharmaceutical manufacturing, validation, operations, or engineering Proven validation expertise in Process and Packaging Equipment (OSD), Facilities and Utilities, and Computerized Systems. Strong technical writing skills and experience with GMP documentation Proficiency in risk assessment and risk-based approach to validation activities Experience with Electronic Documentation Management Systems (KNEAT, VEEVA, TRACKWISE) Excellent problem-solving abilities and innovative thinking Apply directly through this advert or contact Kathy Gillen on to get more details on this great opportunity. Applicants must have a 12 month valid work visa for Ireland. LSC do not offer visa or work permit sponsorship.