Team Lead Facilitator Qc (Day Role)

Team Lead Facilitator QC (DAY Role)required by our client a leading pharmaceutical company based in Waterford City. The Team Lead Facilitator QC person will the Quality team on a Full Time, Permanent basis in Waterford.. Key Responsibilities of the role: To Facilitate and lead the QC team to achieve agreed customer service levels Deliver Customer Service level of >95% by testing components/raw materials/finished product/stability samples in an efficient and timely manner Provide coaching, feedback and ongoing support to team members to ensure they have the necessary skills to perform their duties to the required standards Review work schedule in advance to ensure all relevant components and equipment are available Prioritise daily work schedule to ensure effective analysis of product and adherence to Operational schedule and Stability program timelines as required Plan and organise calibration, maintenance and validation of instruments as required Select and assign people to specific projects and tasks Ensure that all QC documentation is completed correctly and right first time Investigate and authorise Out of Specification investigations with QC Analysts Issue and control of worksheets Perform a detailed review of all analytical data generated in QC on raw materials, and finished products as required to meet the production schedule The ideal candidate will be Degree level educated within a scientific discipline Have a knowledge of cGMP, and GMP for Labs requirements. Broad Knowledge of Analytical Techniques and Experience in HPLC/UPLC People management experience Experience in Calibration Systems Operation of Laboratory Instruments skills Experience of Chemicals and Associated Dangers Knowledge of Company Policies, Procedures and Quality Systems cGMP Regulatory Bodies Experience Knowledge & Understanding of the Chemical / Pharmaceutical Manufacturing sector Familiarity with US and European regulatory guidelines. Documentation Compliance experience Report Writing / Technical Report writing skills Computer Systems Validation & GMP Guidelines Interviewing skills Opex mindset to drive and improve performance in QC Skills: QC People Management GMP HPLC Technical Report Writing Benefits: bonus Medical Aid / Health Care pension