Being an Adaptive individual and an experienced professional with a demonstrated history of working in the pharmaceuticals industry for more than 8 years now I have got an opportunity to demonstrate & implement my skillset & expertise in a new industry.Roles & Responsibilities : • Analytical Support for Stability testing of Oral/Personal Care Products.• Global Key Coordinator for Counterfeit product assessment & tracking.• Data backup & Restoration Supervisor for Analytical Lab instruments.• Quality Standard Owner for Ambient Air Emission & LEV Systems.• Compliance to SOP/GMPs/GLP procedures and data integrity.• Analytical support for Root cause analysis for lab investigations.• Alcohol License renewal, procurement & management.

• Analytical Method Development & Pre-Validation for different Formulations. • Providing analytical assistance for Batch related Deviations & investigations. • Performing Stability Analysis of Drug Products (Formulations) as per GLP/cGMP. • Preparation of Method protocols with periodic revision & review of SOP's. • Calibration & maintenance of various laboratory instruments ex. HPLC/Dissolution/Weighing Balance.

• Hands on experience of ELIMS, Docspace & Track wise ETS Systems. • Ensuring execution of Stability testing in a timely & compliant manner. • Participating in customer Audits and Inspections ex: EMA, US FDA. etc. • Support Initiation of deviations and investigations in compliance to GLP/cGMP. • Documentation of all QC activities performed, in accordance to GLP/cGMP.

Completed my project report titled “Studies on Aeromonas Food Isolates” at Bhabha Atomic Research Center (B.A.R.C).