Catalent
Master Scheduler
Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually. Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer and Catalent employee. Greendale is one of Catalent's gummy technology development and manufacturing facilities in North America. The site manufactures organic and vegan-based nutraceuticals via confection to enhance wellness for all consumers. Simply put
we make healthy gummies. Within the Catalent network, we offer a broad range of integrated formulation and analytical services to solve difficult development and manufacturing challenges. The Master Scheduler is responsible for creating and managing the Master Production Schedule (MPS) as well as the short-term production schedule for the Greendale site. This includes coordination with Planning, Operations, Customer Service, and Quality to create a level loaded production schedule that can be executed efficiently. This includes revising the schedule as necessary when changes need to be made. The Master Scheduler requires a thorough understanding of each department and our production processes and operations. This position is 100% based on-site in Greendale, IN with regular working hours from Monday-Friday 8 AM-5 PM. The Role Collaborate with Customer Service, and Project Managers to understand client demand and translate into a long-range Master Production Schedule. Work with Operations, Quality, Project Management, Document Control, and Supply Chain Management to develop the weekly production schedule as well as rolling quarter production plan. Monitor daily shop floor conditions and perform updates to schedule as needed, as well as communicate schedule changes to Operations, Planning, QA, Warehouse, and other departments, escalate to SLT as needed. Work with Operations Personnel, Production Planners and Project Managers to schedule capacity, equipment, and line personnel. Participate in all pre-launch activities as they relate to scheduling requirements. Schedule Support Group activities that impact production Create Work Orders in JD Edwards for Finished Good and WIP jobs. Other duties assigned The Candidate A minimum of a Bachelors degree is required. Concentration in Supply Chain Management, Operations Management, Project Management, or a related field is preferred. 3+ years of Manufacturing scheduling experience required, GMP or Pharmaceutical Manufacturing preferred. Experience with Finite Planning techniques and systems is required. Must be able to demonstrate diplomatic skills and prioritize work accordingly. Ability to effectively present information and respond to questions from peers and management is required. Ability to work effectively under pressure to meet deadlines is required. Must possess excellent analytical and problem-solving skills. Individual may be required to sit, stand, walk regularly and occasionally lift 0-15 pounds. Why You Should Join Catalent Spearhead exciting and innovative projects Fast-paced, dynamic environment High visibility to members at all levels of the organization 152 hours of PTO + 8 paid holidays Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. Personal initiative. Dynamic pace. Meaningful work.
Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually. Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer and Catalent employee. Greendale is one of Catalent's gummy technology development and manufacturing facilities in North America. The site manufactures organic and vegan-based nutraceuticals via confection to enhance wellness for all consumers. Simply put
we make healthy gummies. Within the Catalent network, we offer a broad range of integrated formulation and analytical services to solve difficult development and manufacturing challenges. The Master Scheduler is responsible for creating and managing the Master Production Schedule (MPS) as well as the short-term production schedule for the Greendale site. This includes coordination with Planning, Operations, Customer Service, and Quality to create a level loaded production schedule that can be executed efficiently. This includes revising the schedule as necessary when changes need to be made. The Master Scheduler requires a thorough understanding of each department and our production processes and operations. This position is 100% based on-site in Greendale, IN with regular working hours from Monday-Friday 8 AM-5 PM. The Role Collaborate with Customer Service, and Project Managers to understand client demand and translate into a long-range Master Production Schedule. Work with Operations, Quality, Project Management, Document Control, and Supply Chain Management to develop the weekly production schedule as well as rolling quarter production plan. Monitor daily shop floor conditions and perform updates to schedule as needed, as well as communicate schedule changes to Operations, Planning, QA, Warehouse, and other departments, escalate to SLT as needed. Work with Operations Personnel, Production Planners and Project Managers to schedule capacity, equipment, and line personnel. Participate in all pre-launch activities as they relate to scheduling requirements. Schedule Support Group activities that impact production Create Work Orders in JD Edwards for Finished Good and WIP jobs. Other duties assigned The Candidate A minimum of a Bachelors degree is required. Concentration in Supply Chain Management, Operations Management, Project Management, or a related field is preferred. 3+ years of Manufacturing scheduling experience required, GMP or Pharmaceutical Manufacturing preferred. Experience with Finite Planning techniques and systems is required. Must be able to demonstrate diplomatic skills and prioritize work accordingly. Ability to effectively present information and respond to questions from peers and management is required. Ability to work effectively under pressure to meet deadlines is required. Must possess excellent analytical and problem-solving skills. Individual may be required to sit, stand, walk regularly and occasionally lift 0-15 pounds. Why You Should Join Catalent Spearhead exciting and innovative projects Fast-paced, dynamic environment High visibility to members at all levels of the organization 152 hours of PTO + 8 paid holidays Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. Personal initiative. Dynamic pace. Meaningful work.