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Regulatory Affairs Associate

Functiegebied:
Publicatie datum:
Einddatum:
ID:
2607045006W

Deel deze vacature:

Kenvue is momenteel op zoek naar een:

Regulatory Affairs Associate

Wat we doen

Bij Kenvue realiseren we de buitengewone kracht van dagelijkse verzorging. Gebouwd op meer dan een eeuw erfgoed en geworteld in de wetenschap, zijn we het huis van iconische merken - waaronder NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON'S® en BAND-AID® die je al kent en waar je van houdt. Wetenschap is onze passie; Zorg is ons talent.

Wie we zijn

Ons wereldwijde team bestaat uit ~ 22.000 briljante mensen met een werkcultuur waar elke stem telt en elke bijdrage wordt gewaardeerd. We zijn gepassioneerd door inzichten, innovatie en toegewijd aan het leveren van de beste producten aan onze klanten. Met expertise en empathie betekent een Kenvuer zijn dat je elke dag de kracht hebt om miljoenen mensen te beïnvloeden. We stellen mensen op de eerste plaats, geven er veel om, verdienen vertrouwen met de wetenschap en lossen op met moed - en hebben schitterende kansen voor je klaarliggen! Geef samen met ons vorm aan onze toekomst - en die van jou. Klik voor meer informatie op here.

Rol rapporteert aan:

Regulatory Affairs Manager

Locatie:

Asia Pacific, India, Maharashtra, Greater Mumbai

Werklocatie:

Hybride

Wat je gaat doen

Associate - Regulatory Affairs

This position reports to Regulatory Affairs Manager and is based at Mulund, 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® Brand Adhesive Bandages that you already know and love. Science is our passion; care is our talent. Our global team is made up of ~ 22,000 diverse and brilliant people, passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact the 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.

Role reports to: Manager - Regulatory Affairs

Location: Mulund, Mumbai

Ingredient & Formula Regulatory Compliance (APAC)

  • Perform regulatory clearance of raw materials and formulas for APAC markets.

  • Review ingredient compliance against applicable APAC regulations, including but not limited to: ASEAN Cosmetic Directive China CSAR Japan, Korea, Australia, India cosmetic and chemical regulations

  • Support regulatory assessments for NPD, Base Business, Importation, Rubicon, and Supplier‑driven changes.

  • Document regulatory decisions accurately in internal compliance systems and databases.

Impact Assessment

  • Conduct impact assessments to identify affected products, materials, or suppliers.

  • Support development and execution of mitigation strategies in collaboration with cross‑functional teams.

  • Escalate critical regulatory risks impacting timelines or market access.

Cross‑Functional Collaboration

  • Partner with APAC Regional Regulatory Affairs, R&D, Materials, Safety/Toxicology, Quality, and Supply Chain teams.

  • Act as an APAC ingredient compliance point of contact for assigned portfolios.

  • Coordinate with external regulatory service providers or consultants where applicable.

Implementation & Governance

  • Support implementation of new ingredient regulatory requirements through established governance and change‑control processes.

  • Track execution of compliance actions and support on‑time delivery of regulatory commitments.

  • Contribute to standardization and continuous improvement of APAC ingredient compliance workflows.

Knowledge Sharing

  • Support APAC‑specific training and onboarding initiatives.

  • Participate in cross‑regional alignment sessions to share APAC learnings and best practices.

  • Contribute to development and maintenance of regulatory guidance and work instructions.

What we are looking for

Required Qualifications

  • Master’s in pharmacy, Chemistry / Life sciences with PG Diploma/ certification in Regulatory Affairs.

Desired Qualifications

  • Experience: Minimum 4-5 Years .in FMCG/ Consumer Products industry.

What’s in it for you

  • Competitive Total Rewards Package*

  • Paid Company Holidays, Paid Vacation, Volunteer Time & More!

  • Learning & Development Opportunities

  • Employee Resource Groups 

  • This list could vary based on location/region

*Note: Total Rewards at Kenvue include salary, bonus (if applicable) and benefits. Your Talent Access Partner will be able to share more about our total rewards offerings and the specific salary range for the relevant location(s) during the recruitment & hiring process.

Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment based on business needs, job requirements, and individual qualifications, without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, protected veteran status, or any other legally protected characteristic, and will not be discriminated against on the basis of disability.

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