Laboratory Team Leader

Work Schedule: Monday-Friday, 8:30am-5:00pm EST. 100% On-site at the Greenville, NC site. Position Summary Catalent’s Greenville, NC 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 Role Supervise, guide and oversee learning and development needs for a team of approximately three to six scientists and other laboratory personnel at various levels. 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. Project management and serve as Analytical representative for internal and external clients, both commercial and pre‑commercial and, as required, CMOs. Author and review analytical procedures, validation documents, portions of regulatory submissions for site pre‑commercial and commercial projects relating to Analytical. Other duties as assigned. The Candidate Requires Associate degree in Science‑related field with nine years of professional experience in pharmaceutical analytical chemistry OR; Bachelor’s degree in Science‑related field with eight years of professional experience in pharmaceutical analytical chemistry OR; Master’s degree in Science‑related field with six years of professional experience in pharmaceutical analytical chemistry OR; PhD in a science‑related field with four 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 three years of professional experience. Demonstrable leadership experience at Catalent (including but not limited to participation in Catalent‑sponsored leadership programs such as NGGL, GOLD, LEAD Now, GM Excellence, and GROW) may be considered in place of external experience. Strongly prefer at least one year of Project Manager and Leadership experience. Individual may be required to sit, stand, walk regularly and occasionally lift up to 15 pounds. Benefits Day one benefits! Medical, dental, vision and 401K benefits effective on your first day. 152 hours of PTO + 8 Paid Holidays. Dynamic, fast‑paced work environment. Opportunity to work on Continuous Improvement Processes. Catalent is an Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email confirming your request for an accommodation and including the job number, title and location to View email address on click.appcast.io. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. #J-18808-Ljbffr Catalent