Production Supervisor - FLL

Position Summary You will provide leadership and direction to a multi-shift maintenance staff in support of pharmaceutical manufacturing and packaging operations as part of a value stream functional unit. Works closely with engineering and production value stream managers and supervisors to deliver zero accidents, zero defects, and zero waste through participation in daily performance management and assignment of staff accountability. Works closely with Engineering Supervisor in evaluation and resolution of equipment failures and/or reliability issues. Ensures employee and equipment safety is at the forefront of all activities, planned and unplanned. About the Zebulon Site GSK’s Zebulon site is a global supplier of Respiratory and Solid Dose medicines to patients around the globe and the largest GSK Pharmaceutical secondary manufacturing site in North America. The site is located less than 30 minutes from downtown Raleigh, Wendell, Knightdale, Rocky Mount, Wilson, and Wake Forest. Key Responsibilities Supervise equipment maintenance in support of value stream production shift operations. Plan resources with Value Stream Engineering Manager. Supports the EHS Zero Accident Prevention Process (ZAP). Perform weekly Workday employee time keeping including approval and monitoring of overtime. Support GPS performance management via daily walk through and performance accountability area meetings. Actively participate in the execution of Root Cause Analysis (RCA) for production downtime over agreed targets. Ensure SAP Preventative Maintenance Plans are planned, delegated, and executed on time to prevent Y3 engineering deviations. Drive Continuous Improvement through weekly maintenance meetings focusing on failure rate analysis of weekly line performance. Coordinate Continuous Improvement projects with engineering supervisor. Performs/leads all duties in accordance with Zebulon Safety Procedures, cGMPs and is subject to the scrutiny of regulatory agencies. Coordinates the engineering technicians (ET) overall capability in new technologies and systems by 70/20/10 principles of GSK development framework. Benefits Clean and GMP compliant work environment Onsite cafeteria Onsite gym Licensed onsite Health & Wellness clinic Temperature-controlled climate Basic Qualifications Two Year Degree in a science or engineering related discipline or 10+ years plus experience in an equivalent maintenance lead role such as Maintenance Lead, etc. 3+ years of experience of pharmaceutical processes, systems, equipment and applicable government regulations Preferred Qualifications Excellent knowledge of cGMPs. Strong written and oral communication skills. Proficient in equipment troubleshooting. Good management skills. Technical expertise in P&ID nomenclature, instrumentation and electrical wiring diagrams. Proficient in SAP (work orders, history, maintenance plans). Good knowledge of cGMPs, and experience in an FDA regulated environment. Equal Opportunity Employer GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law. #J-18808-Ljbffr GlaxoSmithKline