Facilitator Operations R&D Production

Who we areWe touch the lives of over 200 million patients every day, and billions every year. After all, everyone needs healthcare or medication at some point. We're Teva, a global pharmaceutical company, committed to increasing access to high-quality healthcare to patients around the world. We would like to invite applications for the role of Facilitator Operations (R&D Production) at our Waterford site 18 month FTC. This is a two shift position The Facilitator Operations (R&D Production ) role is to manage and facilitate the day to day running of the process teams to meet the objectives of the R&D Operations Function. A Day in the Life of our Facilitator Operations (R&D Production ) To deliver Customer Service level > 95% through schedule adherence (due date compliance at each process date) in accordance with quality standards and cost control. To review departmental performance, identify areas for improvement (NVAs and key variances) and take corrective action as required to ensure continuous improvement in accordance with company policies and procedures. To ensure that all work carried out is in compliance with the required standards and operators have the required training to conform to company, cGMP, Environmental, Health & Safety and regulatory requirements. Plan, direct and monitor departmental projects against schedule and within agreed costs in accordance with Company deadlines. To generate and progress documentation associated with all aspects of manufacturing and Packing processes. To ensure all batch documentation (including SAP) is completed right first time within 48 hours of batch finish as measured by QA (i.e. correct and in full) in order to achieve Customer Service & Good Manufacturing Practice To actively champion and participate in the team working activities where relevant (both internal and external to the department) as part of the Continuous Improvement initiative. To ensure that team members and key task representatives are given the coaching and support required to perform their duties to agreed standards of performance and in line with Company Performance Management System. Plan and agree weekly schedule with the cross-functional schedule agreement team. Organize key task representatives ensuring that sufficient time is planned to carry out duties involved. Who we are looking for Are you…. Educated to Degree level or strong pharmaceutical industry experience Do you have? Knowledge of cGMP requirements Knowledge of cGMP Regulatory Bodies Knowledge of Employment Legislation Knowledge of Company Policies and Procedures Experience of Technical Report Writing Experience of Budget Management Documentation review and compilation