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Quality Chemical Laboratories (QCL), a Wilmington pharmaceutical testing, manufacturing and development lab, seeks a Formulations/Manufacturing Development Director to lead the formulation development laboratory and GMP manufacturing/packaging operations. The role focuses on solid oral dosage forms, with growth into other dosage forms.
The ideal candidate will hold a college degree with 3–5 years in formulation development and GMP manufacturing, and familiarity with analytical techniques and
Quality Chemical Laboratories (QCL), a pharmaceutical testing, manufacturing, and development lab in Wilmington, is seeking a highly motivated leader for our formulation development laboratory and GMP manufacturing/packaging operations. The successful candidate will possess strong leadership skills, problem solving abilities, and a positive can-do attitude. The focus of this position is solid oral dosage forms, but other dosage form experience will be considered as this is an area of growth for the company. Must be capable of working independently from concept and product prototype through cGMP Manufacturing.
The ideal candidate will possess a college degree with 3-5 years’ experience in formulation development and GMP Manufacturing. Familiarity with analytical techniques, regulatory requirements, and early phase cGMP manufacturing is preferred. The Formulations/Manufacturing Development Director will interface with clients, Project Management, Business Development, Supply Chain and Analytical Support while overseeing the Formulations team. QCL offers competitive salaries commensurate with experience and an excellent benefits package as well as great potential for career advancement and leadership in a rapidly growing company.