Elusav Recruitment have an amazing opportunity for a Quality Control Manager with a leading global biopharma company in Waterford, Ireland. As theQuality Control Manager you willensure the provision of an efficient, independent product assessment capability to verify that all products are manufactured consistently, meeting pre-defined specifications and requirements. Responsibilities: To lead all aspects of product quality testing proactively and in accordance with cGMP. To ensure the availability of adequate facilities, trained personnel and approved procedures for sampling, inspecting and testing starting materials, packaging materials, intermediate, bulk and finished products and monitoring environmental conditions for GMP purposes. To be responsible for improvement in cycle times in all QC related activities. To ensure spending is forecasted and executed in accordance with agreed budgets. To ensure that the customer requirements for the QC organisation are clearly understood and agreed and are consistently and reliably met. To provide people leadership to the team, including developing and maintaining succession plans for the QC teams. To be an active contributor to the QO&MPT Leadership team. Ability to work contribute as part of the management ream to the overall success of the site and build strong cross functional relationships. To ensure effective flexible and efficient deployment of available resources, including the proactive transfer to resources between QC teams to meet varying workloads. To provide a proactive and effective support for operational cGMP compliance activities and HSE initiatives in line with site systems. To manage the safety performance of QC according to national legislation, site procedures and other initiatives. Requirements: Significant Experience of working in a cGMP manufacturing environment. Degree in Science (Chemistry, Microbiology or Pharmacy preferred). Post-graduate studies as appropriate to augment primary degree is preferred. Previous Lab Management or Team Leader experience is essential. Operational experience of quality laboratories in a fast-moving manufacturing environment. Detailed knowledge of quality management systems. Effective technical knowledge of pharmaceutical plants. Knowledge of requirements for cGLP, pharmacopeial methods and stability. Full understanding of relevant quality and compliance regulations. Able to manage projects to plan/budget. Effective facilitator. Good communication skills at organisation, team, and individual levels. Understands KPIs for the site. Contact: If you would like to learn more about the vacancy, apply now, or contact Thaissa Torres on or. Skills: Pharma GMP GLP