Full Time

Executive Regulatory Affairs

Kenvue
Mumbai, Hybrid
₹10 - ₹14 LPA
Posted 16/01/2026

About the Role

Roles & Responsibilities
• Provide timely regulatory support for Skin Health and Essential Health portfolios
• Ensure right-first-time dossier submissions and compliant product registrations
• Review and approve product artworks through the Artwork Management System
• Manage regulatory submissions and authority responses (CDSCO, State FDAs, ASCI)
• Track and interpret Indian regulatory changes for cosmetics, OTC, and commodities
• Support policy shaping and proactive regulatory risk mitigation
• Ensure audit readiness with zero critical regulatory observations
• Review and approve product claims and promotional materials as per regulations


Qualification

• Master’s degree in Pharmacy or Science
• PG Diploma or Certification in Regulatory Affairs


Experience

• 6-7 years of hands-on experience in Indian cosmetics and commodities regulatory affairs
• Exposure to drugs regulations (including NPPA) preferred
• Experience with medical device regulations is an added advantage


Skills

• Strong knowledge of Indian regulatory frameworks and compliance requirements
• Expertise in dossier preparation and regulatory submissions
• Excellent regulatory interpretation and documentation skills
• Effective stakeholder communication and coordination abilities
• Ability to manage multiple priorities in a fast-paced environment


About the Company

Kenvue is a global consumer health leader behind trusted brands such as Neutrogena, Aveeno, Tylenol, Listerine and Johnson’s, combining science-led innovation with a strong commitment to care, quality, and regulatory excellence to improve everyday health worldwide.

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