CMC Regulatory Affairs Senior/Consultant - Small Molecules
Join our Global Regulatory Affairs team as a CMC Regulatory Affairs Senior/Consultant. Ensure reputed company's small molecule products are developed and maintained in compliance with global regulatory requirements.
Requirements
• 4–6 years of CMC regulatory experience in the pharmaceutical industry
• Proven reputed company in preparing regulatory documentation for FDA, EMA, and Health Canada
• In-depth understanding of drug development, manufacturing processes, GMP, and regulatory frameworks for small molecules
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