To develop, analyse and validate analytical methods in the analytical department in accordance with cGLP compliance.
Key Responsibilities
- To develop and validate analytical methods required for the testing of product formulations using techniques such as HPLC/UPLC/GC, Dissolution, Particle size analyzer, Zetasizer, viscosity, surface tension etc.
- To coordinate outside analysis related to Q3 studies such as XRD, Raman, DSC, TGA, SEM, TEM etc.
- To prepare and periodically update the related SOPs
- To perform calibration and maintenance of analytical instruments in the laboratory
- To review drug substance DMFs and literature search for the method development
- To follow valuable documentation practices in the analytical laboratory
- Any other responsibility assigned as and when required.
📌 Sr. Research Scientist-AD (Gurugram)
🏢 Sentiss Pharma
📍 Gurugram
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