LSC have a great contract opportunity for a Quality Specialist to join a pharmaceutical company in Cork. If you have 3 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: Execution of the Quality Risk Management (QRM) & Site Quality Risk Register (SQRR) processes ensuring effective governance, communication and management systems are in place and maintained. Execution of the Quality Internal & External Audit/Inspections preparation and management processes for the Site (including follow up on audit action completion, associated CAPA's, and NC Quality approval). Participate in Site risk assessments. Manages projects effectively to meet strict timelines and achieve established milestones with regular updates to Quality and Site Leadership Teams. Quality Review and Approval of SOPs, Work Instructions and forms from other departments and periodic reviews. Quality review and approval of quality non-conformance (NC) records. Quality point of contact for attendance at Root Cause Analysis meetings. ABOUT YOU - ARE YOUR SKILLS A MATCH? Experience with data integrity as a QA Specialist and with risk management projects and driving improvements. Third level Degree in a science or pharmaceutical discipline. A minimum of 3 to 5 years' experience in a quality or compliance role within the biological and/or pharmaceutical industry 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 at LSC on if you have any more questions about this role Skills: Data Integrity Quality Systems Quality Assurance