

Mumbai, India
Senior Regulatory Affairs & RIMS Consultant | Regulatory Affairs
Local Time - 02:12 PM
About Me
Regulatory Affairs Specialist with 9 years of experience in Indian pharma. I help small pharma, nutra, and biotech companies with:
• SOP drafting Document Control, CAPA, Change Control, Deviation Handling
• Regulatory submissions FSSAI, CDSCO, dossier modules
• RIMS data management and cleanup at scale
• Audit readiness for FDA, WHO GMP, and Schedule M inspections
• Technical and regulatory writing
Previous employers: Abbott India Registration Management Associate, Genpact Lead Associate, RA, AmarDeep Pharma RA Executive.
Education: MSc Bioanalytical Sciences 2015, BSc Microbiology 2013
Available for project based work with 2 7 day turnarounds depending on scope.
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