Piramal Consumer Products Division is a leading consumer care business division for Piramal Pharma Limited. Piramal CPD has strived for customer-centricity and solving routine disrupting problems. since 2009. As part of the over 38-year-old Piramal Group, we are proud to have a rich legacy founded on the values of Knowledge, Action, Care, and Impact, which are evident in how we operate as an organization. We live by our mission statement of "Doing Well and Doing Good." Piramal Consumer Products Division has touched the lives of over 7 crore Indians.
Post : Executive Regulatory Affairs
Job Description
Regulations and Compliance
• Execute tasks as per SOP and work process
• Read and understand all regulatory requirements as per business needs
• Stay updated on new regulations
• Liaise with internal stakeholders to ensure OTIF delivery of projects
Regulatory Review
• Review documents for regulatory compliance
• Conduct review of artworks of assigned products
• Conduct review of labels, pack inserts, promotional material – banners, leaflets, print ads,
• TVC, social media campaigns of assigned products
• Support marketing in evaluating NPDs of assigned projects
Exports, Institutional Sales & Ecommerce
• Search, read and understand regulatory requirements of export markets
• Prepare product dossiers for registration
• Provide all regulatory documents in a timely manner Archive all submissions Update and maintain status of regulatory filings
• Ensure regulatory compliance in export markets post registration
Documentation
• Maintain a repository of regulatory and scientific documents
• Maintain tracker for trademarks, artworks, promotional material, exports, institutional sales
• Archive all regulatory correspondence
Candidate Profile
• MSc (Life Science/ Biology/ Biochem/ Molecular Biology)
OR
• BSc (Life-Sciences/ Biochem /Biotech)/BPharm
• 2-5 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
• Interact and maintain relations with cross-functional team
• Ability to independently manage assigned tasks
• Basic IT knowledge
Additional Information
Experience : 2-5 years
Qualification : M.Sc, B.Sc, BPharm
Location : Mumbai, Maharashtra
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Regulatory Affairs
End Date : 25th January, 2024
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