Senior Research Associate

1. Formulation Development experience with specific dosage forms (e.g., Oral solid, Oral liquid etc.)

2. Expertise in development of formulations with solid dispersions, wurster techniques and handling of low dose and potent molecules

3. Tech transfer documents: MFR, BOM, Stability protocol and report, Photostability protocol and report, Thermal cycle study protocol and report, In use study protocol and report, Reconstitution study protocol and report, Specifications

4. Review of reports. Execution of TT activity

5. Regulatory filing document like 3.2.p.1, PDR (3.2.p.2) and other

6. Stability Data Interpretation.

7. Technology transfer to CMO site and support for SU and EB execution

8. Address to regulatory queries

M. Pharma in Pharmaceutics with 4 to 6 years of experience in formulation development of oral solid and oral liquid dosage forms

Experience in DR and ER Pellets formulations and platform technologies such as Hot Melt Extrusion (HME), Extrusion and Spheronization and other solid dispersion is must.