Catalent
Laboratory Team Leader, AR&D
Catalent's Greenville, N.C. facility specializes in end-to-end turn-key solutions for oral solid dosage forms, including integrated formulation development, analytical services, commercial manufacturing, and packaging. This state-of-the-art facility has had over $100M of investments in recent years and features fit-for-scale capacity with potent handling capabilities, ideal for orphan or targeted drug development. The Laboratory Team Leader laboratory personnel in daily activities providing coaching and feedback to team members. The Laboratory Team Leader provides laboratory support for internal business units and external client pre-commercial and commercial process projects. 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. This position is 100% on-site at the Greenville site. The Role Supervise and support development and growth of chemists/scientists in GMP good documentation practices, understanding client project scope, and laboratory technical skills sets by providing on-the-job training, mentoring and guidance. Resolve conflicts within the group relating to performance and/or workload as well as ensure proper resource allocation within and across teams. Schedule analytical work and review analytical data packets and analysis reports, as appropriate. Responsible for development and performance management of direct reports including training, coaching and mentoring. Lead in the development of a climate of quality and safety within the teams, by identifying and monitoring quality and safety standards. Ensure all work is performed and documented according to approved standard operating procedures, in general compliance with cGMPs and in a timely manner consistent with agreed upon schedules. Maintain proficiency in process and data review within respective scientific field of operation in accordance with job responsibility and function, able to troubleshoot instrument, method and technique-related issues. Initiate and perform investigations for out-of-specification and out of trend results as well as deviations from standard operating procedures; ensure timely and comprehensive investigations in compliance with established internal procedures and root cause analysis techniques. All other duties as assigned. The Candidate Associate degree in Biotechnology, Chemistry or equivalent science degree with 9 years of professional experience in pharmaceutical analytical chemistry or; Bachelor's degree in a science-related field (e.g. Biology, Chemistry, Pharmaceutical Sciences) with 8 years of professional experience in pharmaceutical analytical chemistry or; Master's degree in a science-related field with 6 years of professional experience in pharmaceutical analytical chemistry or; PhD in a science-related field with 4 years of relevant experience in pharmaceutical analytical chemistry. Experience in a Catalent analytical laboratory in a role independently managing client interactions and projects as well as mentoring and training junior analysts may be substituted for 3 years of professional experience. Position requires the ability to lift 10-50lbs, unassisted. Majority of the work day is performed while standing, walking, lifting, pulling, and pushing. Requires bending, squatting, crawling, climbing, and reaching. Some exposure to hazardous chemical and other active chemical ingredients. Why You Should Join Catalent Competitive medical benefits and 401K 152 hours of PTO + 8 Paid Holidays Dynamic, fast-paced work environment Opportunity to work on Continuous Improvement Processes 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 is an Equal Opportunity Employer, including disability and veterans.
Catalent's Greenville, N.C. facility specializes in end-to-end turn-key solutions for oral solid dosage forms, including integrated formulation development, analytical services, commercial manufacturing, and packaging. This state-of-the-art facility has had over $100M of investments in recent years and features fit-for-scale capacity with potent handling capabilities, ideal for orphan or targeted drug development. The Laboratory Team Leader laboratory personnel in daily activities providing coaching and feedback to team members. The Laboratory Team Leader provides laboratory support for internal business units and external client pre-commercial and commercial process projects. 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. This position is 100% on-site at the Greenville site. The Role Supervise and support development and growth of chemists/scientists in GMP good documentation practices, understanding client project scope, and laboratory technical skills sets by providing on-the-job training, mentoring and guidance. Resolve conflicts within the group relating to performance and/or workload as well as ensure proper resource allocation within and across teams. Schedule analytical work and review analytical data packets and analysis reports, as appropriate. Responsible for development and performance management of direct reports including training, coaching and mentoring. Lead in the development of a climate of quality and safety within the teams, by identifying and monitoring quality and safety standards. Ensure all work is performed and documented according to approved standard operating procedures, in general compliance with cGMPs and in a timely manner consistent with agreed upon schedules. Maintain proficiency in process and data review within respective scientific field of operation in accordance with job responsibility and function, able to troubleshoot instrument, method and technique-related issues. Initiate and perform investigations for out-of-specification and out of trend results as well as deviations from standard operating procedures; ensure timely and comprehensive investigations in compliance with established internal procedures and root cause analysis techniques. All other duties as assigned. The Candidate Associate degree in Biotechnology, Chemistry or equivalent science degree with 9 years of professional experience in pharmaceutical analytical chemistry or; Bachelor's degree in a science-related field (e.g. Biology, Chemistry, Pharmaceutical Sciences) with 8 years of professional experience in pharmaceutical analytical chemistry or; Master's degree in a science-related field with 6 years of professional experience in pharmaceutical analytical chemistry or; PhD in a science-related field with 4 years of relevant experience in pharmaceutical analytical chemistry. Experience in a Catalent analytical laboratory in a role independently managing client interactions and projects as well as mentoring and training junior analysts may be substituted for 3 years of professional experience. Position requires the ability to lift 10-50lbs, unassisted. Majority of the work day is performed while standing, walking, lifting, pulling, and pushing. Requires bending, squatting, crawling, climbing, and reaching. Some exposure to hazardous chemical and other active chemical ingredients. Why You Should Join Catalent Competitive medical benefits and 401K 152 hours of PTO + 8 Paid Holidays Dynamic, fast-paced work environment Opportunity to work on Continuous Improvement Processes 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 is an Equal Opportunity Employer, including disability and veterans.