Research Scientist

## Description

• Responsible for execution of Analytical Method Development for **Transdermal and Topical and ODF dosage form** (Assay, Dissolution, Related substances, etc.)
• Responsible for execution of Analytical Method Development for **Adhesion testing**.
• Responsible for execution of Analytical Method Development for **IVRT and IVPT testing**.
• Responsible for execution of Analytical method feasibility activities of drug substance / drug product / excipients.
• Responsible for preparation of protocols / reports / standard operating procedures and Standard Testing Procedures.
• Responsible for following cGLP/cGMP compliance of the Analytical Laboratory, ensuring laboratory safety, Good laboratory practices, Good Documentation practice in the lab and general cleanliness and Training & development activities.
• Monitoring and supporting all method transfer related activities from ARD to the CMO locations.
• Responsible for to execute authorized to sign (as prepared and checked by) for, Certificate of analysis, Calibration record, Specification and Standard test procedure, Method Validation / transfer/Reverse Engineering / protocols and reports, Method equivalency report.

## M.Pharm
It's mandatory the candidate should have working experience in the U.S. regulatory market.
Ideally, the candidate should have graduated from a well-known educational institute (e.g., NIPER, BITS)./ Gate Qualified.
The candidate should have at least 3-4 years of experience in the transdermal dosage formulation department.
The candidate should have prior expertise with instruments such as UTMs, diffusion cells, and dissolving USP types V, VI, and VII.