Ankita Talathi
Senior Process Associate @Tata Consultancy Services
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WORK HISTORY
Senior Process Associate @Tata Consultancy Services
Ensured global regulatory compliance by authoring and maintaining 300+ Safety Data Sheets (SDS) daily using SAP EHS, in accordance with GHS, REACH, and CLP standards across multiple regions. Enhanced chemical safety protocols by conducting detailed hazard and toxicological assessments, resulting in improved classification and labeling accuracy for over 500 products. Support microbial hazard reviews, bioburden evaluations, and documentation for Health Canada, EPA, and REACH. Respond to client inquiries on microbial content, product sterility, and complian Streamlined regulatory operations by leveraging SAP, Salesforce, and ETQ systems to manage data, track compliance metrics, and process submissions for TSCA, Prop 65, SVHC, ROHS, PFAS, and other global regulations. Assist with CAPA investigations, internal audits, and documentation updates. Use Salesforce, SAP, and MS Office for request tracking, reporting, and cross-functional communication. Improved regulatory response time by 30% through coordination of Poison Centre Notifications (PCN) and vendor SDS updates, ensuring timely submissions and document accuracy. Led compliance documentation projects within the Product Support Services Group (PSSG), supporting audits, documentation control, and cross-functional collaboration for clinical, safety, and environmental product standards.
EDUCATION
University of Mumbai
Bachelor of Science - BS, Chemistry and Microbiology
AAPS College of Health, Science and Technology
Diploma Certificate, Pharmaceutical Regulatory Affairs
A. G. High School
SSC, HSC science
SVKM's Narsee Monjee Institute of Management Studies (NMIMS)
Master of Business Administration - MBA, HRM
University of Mumbai
Master of Science - MS, Microbiology
ABOUT ANKITA TALATHI
As a Senior Process Associate at Tata Consultancy Services, I manage and author over 300+ SDSs daily using SAP EHS, ensuring global compliance with regulations like GHS, REACH, TSCA, and Prop 65. By leveraging tools like Salesforce, ETQ, and SAP, I’ve streamlined regulatory workflows, improving response times by 30% and supporting Poison Centre Notifications, vendor SDS updates, and documentation audits. Earlier, as a Quality Control Officer at Micromaster Laboratories, I conducted microbiological and chemical testing, implemented efficiency-driven QC protocols (boosting testing accuracy by 25%), and ensured GMP/ISO 9001 compliance through precise reporting and collaboration with R&D teams. I hold a Master of Science in Microbiology from the University of Mumbai and an MBA in HRM from NMIMS University, combining strong scientific expertise with strategic business and people management skills. Certified in GMP, ISO 9001:2015 QMS, Chemical Safety, and Pharmaceutical Compliance, I combine scientific knowledge, regulatory expertise, and hands-on technical tools such as SAP EHS, Salesforce, ETQ, LIMS, and MS Office to deliver compliant, audit-ready documentation and enhance product safety. I am passionate about contributing to a dynamic Canadian life sciences or pharmaceutical organization where quality, safety, and compliance drive impact.
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