: The incumbent will be responsible for reviewing and finalizing regulatory documents, providing regulatory documents to institutional and ecommerce team, compiling and submitting regulatory dossier to export team, preliminary review of artworks and promotional material, understanding and staying up to date with all relevant regulations, maintaining a repository of regulatory and scientific documents, follow all departmental SOPs. Key Stakeholder: Internal: Marketing, Supply Chain, Quality Assurance, R&D, Sales, Business Development Key Stakeholder: External: Corporate Regulatory, Corporate Legal Reporting Structure: Chief Manager - Medical and Regulatory Affairs MSc (Life Science/ Biology/ Biochem/ Molecular Biology) with 3 years of experience BSc (Life-Sciences/ Biochem /Biotech)/BPharm with at least 5 years of experience Experience: 3 to 6 years of experience Well-versed with regulations such as FSSAI, D&C Act, DMR Act, BIS, Legal Metrology Has a good understanding of the operational processes of FSSAI, DCGI and other regulatory bodies Previous regulatory experience in drugs and/or nutraceutical Ability to critically review manufacturing, pharmacology, pre-clinical and clinical data, reports, literature and documentation
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