Regulatory Affairs Coordinator

Há 13 horas

São Paulo, São Paulo, Brasil Kenvue Tempo inteiro
Regulatory Affairs Assistant

Kenvue is seeking a highly motivated and detail-oriented Regulatory Affairs Assistant to join our team in Sao Paulo, Brazil or Sao Jose dos Campos, Brazil.

About Kenvue

We are a global healthcare company built on over a century of heritage and rooted in science. Our iconic brands, including NEUTROGENA, AVEENO, TYLENOL, LISTERINE, JOHNSON'S, and BAND-AID, are known for delivering high-quality products to our customers. Our team of 22,000 diverse and brilliant people is passionate about insights, innovation, and committed to delivering the best products to our customers.

Job Summary

The successful candidate will work closely with the regulatory LatAm champion on strategic projects in the region and provide support for Local Regulatory. This is an unprecedented opportunity to learn and collaborate with the whole RA process. The Regulatory Affairs Assistant 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 processes linked to RA responsibilities (artworks, dossiers management, and MDM framework).

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

We are looking for a candidate with a Bachelor's degree in progress by Q4'2025 and at least 1 year of professional experience, including internship and/or university research programs. The ideal candidate will have 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, and some knowledge in Cosmetics or Pharma regulations, guidelines, policies, etc. and Health Authorities in LATAM.

What We Offer

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.

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