Result oriented professional with many years of experience in pharmaceutical and consumer health care related industry within a cGMP environment. Worked on various solid, semi-solids, liquid, dosage forms. Performed Method development, Method Validation, Method Verification and Method Transfer. Hands on experience on UPLC (Acvity H-Class), HPLC, GC, Auto-Dissolution USP apparatus I,II and IV(Sotax)Flow through Cell, AA, IR and UV-VIS instrumentation, with excellent analytical, problem solving and troubleshooting skills. Proficient in ANDA complete stability studies and release analysis. Maintaining good documentation practices according to cGMP standards. Good Analytical, communication & interpersonal skills with clear understanding of procedures and quick learner. Familiar with EHS and OSHA regulations. Trained New Hires with proper guidelines and ensured cGMP Procedures are followed. Always met deadlines with reference to ANDA submissions, Manufacture equipment release. Capable of handling multiple tasks. Interprets data (Chromatography, Spectroscopy and physical testing) and performs analytical method transfer to Quality Control following transfer guidelines. Effective time management for completion of projects by planning with Excellent Team co-ordination and support.

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