Description
Kenvue is currently recruiting for:

Regulatory Affairs Assistant (Fixed Term 24 Months)
This position reports into Regulatory Affairs Manager and is based at Sao Paulo, Brazil or Sao Jose dos Campos, Brazil.

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 by 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.

What you will do
The successful candidate will work very close to the regulatory Lat Am champion for strategic projects in the region and provide support for Local Regulatory, which is an unprecedented opportunity to learn and collaborate to the whole RA process. You will hold a position connecting with Local RA and a multifunctional team (Marketing, R&D, Supply Chain, Quality Assurance, Planning and others) to support and deploy the regulatory strategy, besides running process linked to RA responsibilities (artworks, dossiers management and MDM framework).
Additionally, they provide general administrative support as directed:
Key Responsibilities

• Work with different areas by being a point of connection and providing support to local and regional RA.

• Ensure business continuity by supporting proper regulatory strategy definition and execution.

• Identify and communicate effectively local/regional requirements for regulatory submissions.

• Contribute with the revision of technical documentation and with the preparation and compilation of regulatory dossiers.

• Attend project team meetings with RA lead to assist in strategic discussions.

• Review and approve artwork and labels to ensure regulatory compliance.

• Present status updates on regulatory/project activities to key internal partners.

• Partner with RA Liaison and RA Local colleagues to deliver regulatory outcomes.

• Develop and maintain regulatory affairs databases and tracking systems

• Establish accountability for the preparation of necessary outlines, summaries, status reports, memos, graphs, charts, tables, and slides.

• Ensure quality and compliance in all actions.

Qualifications
What we are looking for
Required Qualifications

• Bachelor’s degree in progress by Q4’2025

• At least 1 year of professional experience, including internship and/or university research programs

• Strong attention to detail and organizational skills

• Excellent written and verbal communication skills

• Proficiency in Microsoft Office and database management

• Excellent project and time management skills required

• Some knowledge in Cosmetics or Pharma regulations, guidelines, policies, etc. and Health Authorities in LATAM.

• Strong connection and teamwork skill with ability to work and communication with different partners like Marketing, Local Regulatory, Supply Chain and Quality.

Kenvue is proud to be an 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.

Primary Location Latin America-Brazil-São Paulo-São Paulo

Job Function Regulatory Compliance