LSC have a great contract opportunity for a CSQA for MES to join a Cork based Biotech Drug Substance Manufacturing Facility. If you have at least 5 years of relevant experience in a cGMP environment and ready for your next challenge, this could be the perfect project for you! ABOUT THE PROJECT - KEY RESPONSIBILITIES: Provide Quality leadership, direction, and governance for MES and MES related systems. Investigate and troubleshoot issues relating to MES and MES related systems. Manage Quality-related matters specific to area (Quality system or Quality Program) of responsibility. Approve appropriate quality-related documents. An approval signature confirms that site and GMP requirements have been met. Carry out day-to-day activities in compliance with site safety policies and procedures.? Promote and encourage safe practices and promptly report any safety concerns. Promote and encourage Quality culture and promptly report any compliance concerns. ABOUT YOU - ARE YOUR SKILLS A MATCH? May hold BSc, MSc or PhD in Chemistry, Engineering, or related discipline Experience with MES (Manufacturing Execution Systems) Skilled in digital batch records linked to manufacturing activities For our contracting positions in Ireland's pharmaceutical industry, applicants must possess a Stamp 1G or a Stamp 4 visa. Apply via this advert or contact Cian Marnane at if you have any more questions about this opportunity! Skills: Manufacturing Execution System (MES) Digital Batch Records Manufacturing