Formulations Scientist: Solid Dose & Parenteral Dev, cGMP

Quality Chemical Laboratories; Wilmington (NC); On-site; USD 80,000 - 105,000; Full time

Benefits offered by this job

Excellent benefits package

Career advancement opportunities

Leadership development

Job summary

Quality Chemical Laboratories in Wilmington seeks a highly motivated scientist for our formulation development laboratory focusing on solid oral dosage forms. The role involves developing formulations from concept to prototype and transferring processes into cGMP manufacturing.

Experience in parenteral dosage forms will be considered as growth for the company. The ideal candidate has a college degree and at least 3 years of formulation development experience, plus familiarity with regulatory

Qualifications

• A college degree is required with at least 3 years’ experience in formulation development.
• Experience in process development and technology transfer into cGMP manufacturing, familiarity with analytical techniques, regulatory requirements, and early phase cGMP manufacturing is preferred.

Responsibilities

• Develop and optimize solid oral dosage formulations.
• Transfer technology into cGMP manufacturing.
• Collaborate with analytical and regulatory teams.
• Work independently from concept through product prototype to transfer to manufacturing.

Skills

Problem solving

Customer service

Independent work

Formulation development

Education

Bachelor's degree

Job description

Quality Chemical Laboratories in Wilmington seeks a highly motivated scientist for our formulation development laboratory focusing on solid oral dosage forms. The role involves developing formulations from concept to prototype and transferring processes into cGMP manufacturing.

Experience in parenteral dosage forms will be considered as growth for the company. The ideal candidate has a college degree and at least 3 years of formulation development experience, plus familiarity with regulatory