Senior QC AnalystMy client, a global pharmaceutical company, who specialises in developing, registering and manufacturing of both human generic and veterinary pharmaceutical products, seeks to hire a new Senior QC Analyst. This role will suit someone with a 3rd level education in chemistry and experience working in people management and as a Quality Control Analyst, who wishes to grow their career in a world-renowned organisation. This is a permanent position, based on site at their headquarters in East Co. Galway. ResponsibilitiesUnderstand how to demonstrate technical proficiency in the following areas: HPLC, IR, UV, dissolution & physical testing. Ensuring that laboratory always meets GLP/GMP standards. To maintain all laboratory logbooks and document all records relating to Quality Control and store accordingly. Maintain and follow all relevant Standard Operating Procedures (SOP’s). Provide a full analysis of contract manufactured products in accordance with customer specifications. Full analysis of finished products, including tablets, boluses and veterinary drenches. This to be completed using appropriate analytical techniques. Provide samples for external analysis when requested. Participating in internal/External Audits. Support the laboratory testing schedule to achieve an efficient QC system and Customer Service level of >95%. Follow up on Corrective Actions. Responsible for communication with external suppliers and vendors, in relation to QC consumables. Requirements 3rd level Qualification in a chemistry-based discipline. 4+ years' experience as a QC Analyst. Experience in people management. Knowledge of US FDA guidelines. Experience working in a pharmaceutical cGLP environment. For more information, please contact #LI-DC6