• Independently Handle Instruments Like LCMS, ICP MS, Ion Chromatograph, GC HSMS, HPLC, UV, Gas Chromatography, Atomic Absorption Spectroscopy and Titration.
• Desired candidate should be independently develop or validate methods for parameters like Assay, Dissolution and Related Substances
• Perform analysis on Finished Drug Products.
• In depth knowledge of Qtegra, Analyst and Chromeleon software.
• Integrate Peaks and Perform Calculations for Analysis Done.
• Independently Report the Analysis.
• Preparation of Analytical Method Development Reports, Analytical Development Validation Reports, Standard Testing Practices, Certificate of Analysis and other analytical related documents.
• Knowledge of Extractable and Leachable will be a plus.
• Maintain GLP Requirements.
• Have adequate knowledge about Quality Management Systems.
• Independently Perform analysis like Assay, Dissolution, Content Uniformity, Forced Degradation & Related Substance.
• Should be able to calibrate instruments
• Candidate should have "Go-Getter" Attitude and be a Team Player
• Candidates ready to join will be preferred.

Contact - Mohit Kowani - HR

This is a walk-in to proceed further contact HR at the venue on date and time mentioned.

Fusion Scientific Laboratories Pvt. Ltd. is an US FDA approved contract research organisation providing services pertaining to Formulation Development and Analytical Services to pharmaceutical companies globally catering to regulated markets like Us, Canada, Australia, UK, Gulf and more.