Regulatory Affairs Associate

我们做什么

在 Kenvue，我们意识到日常护理的非凡力量。我们以一个多世纪的传统为基础，植根于科学，是标志性品牌的品牌 - 包括您已经熟悉和喜爱的 NEUTRGENA®、AVEENO、TYLENOL®®、LISTERINE®、JOHNSON'S® 和 BAND-AID®。科学是我们的热情所在;关心就是我们的才能。

我们是谁

我们的全球团队由 ~ 22,000 名才华横溢的员工组成，他们的职场文化中，每个声音都很重要，每一个贡献都受到赞赏。 我们热衷于洞察， 创新并致力于为我们的客户提供最好的产品。凭借专业知识和同理心，成为 Kenvuer 意味着每天有能力影响数百万人。我们以人为本，热切关怀，以科学赢得信任，以勇气解决——有绝佳的机会等着您！加入我们，塑造我们和您的未来。有关更多信息，请单击 here.

Role reports to：

Global Ingredient Management Director

位置：

Asia Pacific, India, Maharashtra, Greater Mumbai

工作地点：

混合

你会做什么

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.

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