Formulations/Manufacturing Development Director

Clay Today; Wilmington, Northern (NC, KY); Hybrid; USD 120,000 - 180,000; Full time

Benefits offered by this job

Competitive salary

Excellent benefits package

Job summary

Quality Chemical Laboratories (QCL) in Wilmington, NC seeks a Formulations/Manufacturing Development Director to lead our formulation development laboratory and GMP manufacturing/packaging operations. The role focuses on solid oral dosage forms, with growth opportunities across other dosage forms as needed.

The ideal candidate has a college degree and 3-5 years of experience in formulation development and GMP manufacturing, with familiarity in analytical techniques, regulatory requirements, and

Qualifications

• 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.
• Experience interfacing with clients, Project Management, Business Development, Supply Chain and Analytical Support.

Responsibilities

• Lead the Formulations/Manufacturing Development laboratory and GMP manufacturing/packaging operations.
• Oversee the Formulations team and coordinate with clients, Project Management, Business Development, Supply Chain and Analytics.
• Ensure compliance with regulatory requirements and cGMP standards.

Education

Bachelor's degree in a relevant field

Job description

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.