Job Description:
Develop and validate analytical methods for testing of product formulations, finished products, raw materials, and APIs using techniques such as HPLC/UPLC/UV/GC/IC, Dissolution, Particle Size Analyzer, Zetasizer, Viscosity, Surface Tension, and wet chemical methods.
Prepare method development reports from developmental trials, method validation/verification protocols and reports, Specifications, STPs, and Certificates of Analysis from routine analysis and vendor documents.
Perform analysis of raw materials, APIs, and excipients as per Pharmacopoeial/vendor methods, including analysis of routine and stress samples of finished products.
Prepare method transfer sheets and transfer analytical methods to plant QC.




Coordinate outside analysis related to Q3 studies such as XRD, Raman, DSC, TGA, SEM, TEM, etc.
Review drug substance DMFs and conduct literature searches to support method development.
Prepare and periodically update relevant SOPs; perform calibration and maintenance of analytical instruments in the laboratory.
Follow valuable documentation practices and perform all analytical activities in compliance with cGLP.
Handle any other responsibilities assigned as required.

Experience Required: 3–10 years
(Designation will be offered based on candidate's experience and skill set)

📌 Research Scientist/Senior Research Scientist (Gurugram)
🏢 Sentiss Pharma
📍 Gurugram