Executive-Regulatory Affairs

This position reports to Associate Manager-Regulatory Affairs and is based at Mumbai.

Who We Are

At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent. Our global team is made up with 22,000 diverse and brilliant people, passionate about insights, innovation and committed to deliver the best products to our customers. With expertise and empathy, being a Kenvuer means to have the power to impact life of millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours. For more information, click here.

What you will do

The Executive-Regulatory Affairs is responsible contribute regulatory expertise in various aspects including regulatory submissions, right first-time dossiers, timely addressal of queries, etc. for various product categories such as Cosmetics, Drugs and Food products etc. and in external engagements, while maintaining regulatory compliance to achieve the organization's expectations for productivity, quality, and goal accomplishment:

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Key Responsibilities:

· On-time regulatory support for all existing as well as upcoming projects including for Selfcare (Drugs], Skin Health & Essential Health, along with maintaining regulatory compliance for flawless execution, right first-time dossier submission and speedy product registrations in compliant manner.

· Approvals of artworks in Artworks system for respective products in Selfcare (Drug], Skin Health & Essential Health Franchise.

· Stay updated on current changes in regulatory environment in various markets on OTC, Cosmetics policies/regulations and use them appropriately to support in local policy & relation shaping.

· Foreseeing & supporting any possible changes in policies that will enable JNTL Consumer Health (India) to act in timely manner.

· Ensuring timely responding to regulatory queries including CDSCO, State Drug Control offices, ASCI, etc.

· Ensuring no critical regulatory findings in internal & external audits. Ensure compliance to both external regulatory requirements & internal systems.

· Ensure timely approval of claims & promotional materials for Selfcare (Drugs),Skin Health and Essential Health portfolio while ensuring regulatory compliance.

Qualifications

What We Are Looking For

EDUCATION:

Required Oualifications

· Master's in pharmacy / science with PG Diploma/ certification in Regulatory Affairs.

Desired Qualifications

· Experience: Minimum 6 to 7 Years in Indian cosmetics, Drugs (including NPPA related work], medical devices, and commodities regulatory domain.

· Skills: Adequate regulatory and technical knowledge in cosmetics, drugs, medical devices and commodities portfolio, proficiency in law interpretation skills, effective interpersonal skills, and with high adaptability, in a complex environment with strong work ethics.