To work for an organization that will assign challenging job in order to bring out best of my talent utilizing my skills to the fullest and offer me learning experience so that I may be able to achieve desired goals of mine and those of the organization.
Overview
2025
2025
years of professional experience
2006
2006
years of post-secondary education
2
2
Languages
Work History
Sr. Executive
Sun Pharmaceuticals Industries Limited
01.2015 - Current
Product Release as per SOP
To give usage decision for intermediates
Filling of Vendor Questionnaire
Review of analytical data
Preparation of annual product quality Review
To assist in handling of customer queries
To assist in handling of market complaints
Review of Batch Processing record and verify the compliance as per applicable review check list
Review of customer’s quality assurance agreements and ensure their compliance
Daily plant round to maintain quality system in production according to cGMP
Executive
Panacea Biotec Limited
12.2012 - 01.2015
Product release and its proper documentation
Review and updation of Site Master File (SMF)
Review and updating the QA SOP’s
Handling of change control and deviations
To maintain quality system in production according to cGMP
Analysis of in-process sample
Review of batch production record
Issuance and control of documents
Preparation of annual product quality review
Coordination with other departments like Production, Quality Control, Supply Chain Management, and R&D etc
For compliance of day to day requirements in the facility
Sr. Officer
Ind-Swift Laboratories Ltd.
4 2007 - 12.2012
Company Overview: USFDA APPROVED
Product release and its proper documentation as per product release SOP
Review of analytical data
Timely and accurate filling of vendor questionnaire
To assist in handling of customer enquiry
Handling of returned material
To assist in handling of market complaints
Review of customer’s quality assurance agreements and ensure their compliance
Handling of change control, deviations & amendments
To maintain quality system in production according to cGMP
Preparation of material safety data sheet
To perform the Internal Audit
To provide key input into the preparation, amendment and harmonization of procedures
Issuance of analytical protocol and raw data sheet