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Regulatory Affairs Associate

Функция работы:
Дата публикации:
Дата окончания:
ID:
2507036069W

Поделиться этой вакансией:

Kenvue в настоящее время набирает сотрудников на:

Regulatory Affairs Associate

Что мы делаем

At Kenvue, мы осознаем необычайную силу повседневной заботы. Основанный на более чем вековом наследии и уходящий корнями в науку, мы являемся домом культовых брендов, включая NEUTROGENA®, AVEENO,® TYLENOL,® LISTERINE,® JOHNSON'S® и BAND-AID®, которые вы уже знаете и любите. Наука – наша страсть; забота – это наш талант.

Кто мы

Наша глобальная команда – это ~ 22 000 блестящих людей с культурой рабочего места, где каждый голос имеет значение, а каждый вклад ценится. Мы увлечены идеями, инновации и стремление поставлять нашим клиентам лучшие продукты. Обладая опытом и эмпатией, быть Kenvuer означает иметь возможность влиять на миллионы людей каждый день. Мы ставим людей на первое место, заботимся о настолько, завоевываем доверие наукой и смело решаем – и вас ждут блестящие возможности! Присоединяйтесь к нам, чтобы формировать наше будущее и ваше. Для получения дополнительной информации, нажмите here.

Role reports to:

Global Ingredient Management Director

Местонахождение:

Asia Pacific, India, Maharashtra, Greater Mumbai

Место работы:

Гибрид

Что ты будешь делать

Kenvue is currently recruiting for:

Regulatory Affairs Associate

The job location is 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

Kenvue is looking for a highly skilled and detail-oriented Regulatory Affairs Associate for Cosmetics, Commodities and Packaging within our Global portfolio. In this role, you will manage raw material and formula clearance projects while ensuring compliance with relevant Health authority legislations, Chemical regulatory requirements and Kenvue internal policies. You will support analysis of upcoming regulations and their impacts on our portfolio and collaborate with both internal and external partners to drive compliance initiatives effectively.

Key Responsibilities:

  • Manage raw material, formula and packaging clearance projects, ensuring compliance with relevant regulatory requirements and Kenvue internal policies.
  • Support monitoring and analysis of upcoming regulations affecting our portfolio and assess their implications.
  • Oversee global change control processes and ensure timely execution.
  • Collaborate with internal teams (e.g., Product R&D, Packaging R&D, Regional/ Local Regulatory Affairs, Tech ops, Quality assurance, Safety team, Materials team) and external partners to facilitate clear communication and alignment on compliance matters.
  • Engage with Global stakeholders to ensure cohesive regulatory strategies and project execution.
  • Work as part of a multidisciplinary team to drive compliance initiatives and promote a culture of regulatory excellence.
  • Lead or Partner in Continuous improvements initiatives to bring agility to our work and team.

What We Are Looking For

Experience and Skills:

Required:

  • Masters in Pharmacy or Masters degree in scientific discipline (Chemistry, Biochemistry, Biotechnology, or related field).
  • 5-6 years of relevant experience in regulatory affairs in FMCG, particularly in ingredient and formula compliance
  • Strong knowledge of Packaging, Commodity and Cosmetic Product regulations and their application.
  • In-depth knowledge of global regulatory requirements and processes related to consumer health products.
  • Excellent analytical, organizational, and project management skills.
  • Strong verbal and written communication abilities, with an emphasis on collaboration and clarity.
  • Proven ability to work effectively in a fast-paced, team-oriented environment with global stakeholders.

Preferred Qualifications:

  • Experience working with industry standards preferred.
  • Ability to manage multiple stakeholders and priorities.

Kenvue is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

Если вы являетесь человеком с ограниченными возможностями, пожалуйста, ознакомьтесь с нашим страница помощи инвалидам для получения информации о том, как запросить приспособление.