Position Details
About this role
Director/Associate level process engineer for oral solid dosage formulation, responsible for experimental design, process development, and technology transfer from R&D to manufacturing with regulatory submissions.
Key Responsibilities
- Independently design, execute, interpret experiments
- Master new techniques
- Innovate protocols
- Coordinate with cross-functional teams
- Write internal reports and support regulatory submissions
Technical Overview
Hands-on lab-based formulation development, scale-up expertise, regulatory submission experience, and cross-functional collaboration across clinical development and manufacturing.
Ideal Candidate
The ideal candidate is a mid-level process engineer with 5+ years in oral solid dosage formulation and technology transfer, capable of independently designing experiments, scaling processes, and communicating effectively across R&D and manufacturing teams.
Must-Have Skills
Nice-to-Have Skills
Required Skills
Hard Skills
Soft Skills
Industry & Role
Keywords for Your Resume
Deal Breakers
Lack of hands-on formulation or scale-up experience, Inability to work in a lab-based, regulated environment, No experience with technology transfer in pharma
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