Formulations/Manufacturing Development Director

Quality Chemical Laboratories; Wilmington (NC); On-site; USD 120,000 - 180,000; Full time

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. This role emphasizes solid oral dosage forms and independent work from concept to cGMP production.

The ideal candidate has a college degree and 3–5 years in formulation development and GMP manufacturing, with familiarity in analytical techniques, regulatory requirements, and early phase cGMP

Qualifications

• 3–5 years experience in formulation development and GMP manufacturing.
• Exposure to regulatory requirements and analytical techniques.
• Experience leading cross-functional teams is a plus.

Responsibilities

• Lead the Formulations team across development and GMP manufacturing.
• Oversee concept through cGMP production for solid oral dosage forms.
• Interface with clients, Project Management, Business Development, Supply Chain and Analytical Support.

Skills

Leadership

Problem solving

GMP Manufacturing

Formulation development

Analytical techniques

Regulatory requirements

Early phase cGMP

Client interfacing

Education

Bachelor's degree

Job description

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.