Job Details: Job Location: DifGen Pharmaceuticals Pvt Ltd- R&D - Prashanti Nagar IE Kukatpally Hyderabad, TELANGANA, Salary Range: Undisclosed, Job Shift: Day, 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.