Manufacturing Supervisor - 2nd Shift

Work Schedule Second Shift (Afternoons) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Strong Odors (chemical, lubricants, biological products etc.) Job Description As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. Schedule: Monday-Friday, with some weekend work required Hours: 2:30pm-11pm Responsibilities Commitment to safety, by following site safety procedures and enforcing safety PPE requirements on the production floor. Ability to report hazards, near misses, and incidents. Enforce quality standards with the production operators, including adherence to cGMP standards, procedure adherence, and formula specifications met. Assign work activities for daily production. Enforce schedule pacing and adherence. Investigate and report deviations related to the manufacturing formulas and yield variances. Coordinate with production scheduler on schedule misses. Build effective teams through leadership, training, performance management, and career development. Perform batch record review and ERP transactions for production related activities. Maintain shift log that provides direct written communication to the subsequent shifts pertaining to special instructions and information. Actively contribute to 5S and PPI efforts within the production area. Maintain departmental Key Performance Indicator metrics. Train and document new colleagues or current colleagues in new skills or retraining; including safety, quality, and SOPs. Review and maintain accurate quality records as they relate to production. This includes cleaning logs, chart records, PM related documents, etc. Active contribution to resolving unplanned deviations. Use of RCA tools such as 5-why and fishbones. Requirements Bachelor’s Degree plus 5 years of manufacturing experience, with 2+ years in a supervisory/leadership role Preferred Fields of Study: Engineering, Science, Business or related technical field Experience in GMP/ISO regulated manufacturing environment preferred #J-18808-Ljbffr Dormont Manufacturing Co