Regulatory affairs specialist – São Paulo/SP

Responsabilidades

• Ensuring the regulatory compliance of all products commercialized by the company in Brazil and LATAM.
• Acting as the local regulatory authority, working independently while coordinating closely with R&D, Quality, Purchasing, Operations and external manufacturing partners.
• Managing all regulatory documentation and product registrations.
• Tracking regulatory changes.
• Supporting audits with regulatory evidence.
• Ensuring timely, accurate compliance for new and existing products.

Requisitos

• Bachelor’s degree in Pharmacy, Chemistry, Chemical Engineering, Biology, or related scientific fields.
• 5–10 years of experience in Regulatory Affairs in the chemical, automotive, cosmetics, or pharmaceutical industries.
• Proven experience with product registrations, SDS creation/review, labeling compliance and regulatory audits.
• Strong understanding of ANP, ANVISA, MAPA and Inmetro requirements.
• English: Advanced (daily meetings with global/regional teams).
• Spanish: Advanced (constant interaction with LATAM teams & authorities).
• Highly autonomous, detail-oriented regulatory professional ready to take the lead locally.

Marcado como: ANVISA, Assuntos Regulatórios, Cosméticos, Indústria Automotiva, Indústria Química