What are the responsibilities and job description for the Formulations/Manufacturing Development Director position at Quality Chemical Laboratories?
Formulations/Manufacturing Development Director
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.
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