Research Associate/ Scientist FRD

Job ID 17-00249

Industry Pharma

Job Type Permanent

Location Denville, NJ


- Execute experimental studies to support the development of solid oral dosage forms
- Review, compilation, evaluation, interpretation and reporting of experimental results.
- Prepare batch manufacturing records, protocols and reports as assigned
- Prepare Regulatory submission (PDR, QOS etc.) documents including writing CMC and formulation development reports.
- Knowledge of current FDA guidelines for product development. 
- Prepare the batch records/protocols
- Maintain experiment lab notebooks and equipment log books.
- Coordinate handling of Controlled Substances.
- Performs other related duties as assigned and prioritized by supervisor


- 3-4 years' experience in generics formulation development of Oral Solid dosage forms such as immediate release, extended release and delayed release dosage forms.

- Hands on experience with High Shear Granulator, Fluid Bed Drier, GPCG, Blender, Monolayer / bilayer Compression Machine and Coating Machine.