Oral Solid Dosage Formulation Scientist - Tech Transfer

Atrium Staffing LLC; Cranbury Township (NJ); On-site; USD 70,000 - 105,000; Full time

Benefits offered by this job

Medical

Dental

Vision

Job summary

Atrium Staffing LLC is seeking an experienced Oral Solid Dosage Formulation Scientist for a pharmaceutical development client in New Jersey. The role focuses on developing and optimizing tablets, capsules, and oral liquids with minimal supervision.

You will scale up processes, transfer technology to manufacturing, and prepare technical documents while applying QbD and regulatory guidelines. Collaboration across PM, Manufacturing, Analytical R&D, QA, and external customers is essential.

Qualifications

• Direct pharmaceutical formulation development experience in oral solid dosage required.
• Experience with tablets, capsules, and oral liquids is essential.
• Demonstrated hands-on formulation development and tech transfer experience.
• Familiarity with cGMPs and safety practices.

Responsibilities

• Independently design and optimize oral solid dosage formulations.
• Develop and execute product development and technology transfer plans.
• Draft SOPs, proposals, batch records, protocols, and regulatory documents.
• Mentor junior scientists and work with cross-functional teams.
• Apply QbD principles and ensure regulatory compliance.

Skills

Oral Solid Dosage

Formulation Development

Tech Transfer

cGMP

Project Management

Communication

Education

B.S. in Pharmaceutical Sciences

M.S. in Pharmaceutics

Ph.D. in Pharmaceutical Sciences

Tools

Fluid Beds

High Shear Granulators

Roller Compactors

Tableting

Coating Machines

Blenders

Mills

Job description

Atrium Staffing LLC is seeking an experienced Oral Solid Dosage Formulation Scientist for a pharmaceutical development client in New Jersey. The role focuses on developing and optimizing tablets, capsules, and oral liquids with minimal supervision.

You will scale up processes, transfer technology to manufacturing, and prepare technical documents while applying QbD and regulatory guidelines. Collaboration across PM, Manufacturing, Analytical R&D, QA, and external customers is essential.