Regulatory Affairs Specialist

4 semanas atrás


Brasil Kenvue Tempo inteiro
Regulatory Affairs Assistant

Come work at the forefront of science and help iconic brands grow and evolve into the next generation.

This position reports into the Regulatory Affairs Manager and is based at Sao Paulo, Brazil or Sao Jose dos Campos, Brazil.

About 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.

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.

Key Responsibilities
  1. Work closely with the regulatory LatAm champion on strategic projects in the region and provide support for Local Regulatory.
  2. Ensure business continuity by supporting proper regulatory strategy definition and execution.
  3. Identify and communicate effectively local/regional requirements for regulatory submissions.
  4. Contribute to the revision of technical documentation and the preparation and compilation of regulatory dossiers.
  5. Attend project team meetings with RA lead to assist in strategic discussions.
  6. Review and approve artwork and labels to ensure regulatory compliance.
  7. Present status updates on regulatory/project activities to key internal partners.
  8. Partner with RA Liaison and RA Local colleagues to deliver regulatory outcomes.
  9. Develop and maintain regulatory affairs databases and tracking systems.
  10. Establish accountability for the preparation of necessary outlines, summaries, status reports, memos, graphs, charts, tables, and slides.
  11. Ensure quality and compliance in all actions.
Requirements
  1. Bachelor's degree in progress by Q4'2025.
  2. At least 1 year of professional experience, including internship and/or university research programs.
  3. Strong attention to detail and organizational skills.
  4. Excellent written and verbal communication skills.
  5. Proficiency in Microsoft Office and database management.
  6. Excellent project and time management skills required.
  7. Some knowledge in Cosmetics or Pharma regulations, guidelines, policies, etc. and Health Authorities in LATAM.
  8. Strong connection and teamwork skill with ability to work and communicate 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.



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