WhatsApp Group
Join Now
WhatsApp Channel
Join Now
Telegram Group
Join Now

Antal International Hiring Regulatory Affairs Specialist

Published on

Antal International

B.Pharm, M.Pharm, Pharm.D, Msc, BSc

Not disclosed

Mumbai, Maharashtra, India

4-8 years

Verified Job

Skills Required

  • Regulatory Documentation
  • Tax Deducted at Source (TDS)
  • GHS (Globally Harmonized System)
  • CLP (Classification, Labeling, and Packaging)
  • US OSHA (Occupational Safety and Health Administration)
  • Canadian HPR (Hazardous Products Regulations)
  • China GHS
  • IATA (International Air Transport Association) regulations
  • IMDG (International Maritime Dangerous Goods) transport regulations
  • HALAL and Kosher certification
  • COA (Certificate of Analysis)
  • TDS (Technical Data Sheet)
  • MSDS (Material Safety Data Sheet)
  • Process improvement and automation
  • Chemistry knowledge

Responsibilities

  1. Lead the technical and regulatory documentation for smooth operations.
  2. Ensure accuracy and quality of COA, TDS, MSDS, and other related technical documents.
  3. Maintain a real-time database of products and suppliers with corresponding technical documents.
  4. Mentor and guide the documentation team on best practices and processes.
  5. Support the demand and supply team with suitable inputs on specifications.
  6. Manage regulatory information, certificates, and declarations.

Application Link

Share This Job

✅ Job Copied Successfully!

PharmaBharat Editorial Team

The PharmaBharat Editorial Team, comprised of pharmaceutical industry experts with over 3 years of collective experience in research, regulatory affairs, and market analysis, delivers accurate and timely updates on trends, innovations, and career opportunities. Our content is rigorously vetted by professionals with advanced degrees in pharmacy and biotechnology, ensuring authoritative and trustworthy insights for job seekers in the pharmaceutical sector.