SP l São Paulo
Efetivo (CLT)
Biólogo
Biomédico
Farmacêutico
Responsabilidades
- Support business objectives by proactively providing regulatory guidance and information at both substance and product levels to ensure compliance with applicable chemical regulations across the region.
- Proactively monitor regulatory developments (existing and emerging requirements) related to chemical regulations and assess their impact on the company’s business, providing guidance and recommendations.
- Lead or facilitate substance registrations and notifications with regulatory authorities in Mexico, Central America, and South America.
- Represent the company in industry associations and maintain relationships with regulatory authorities.
- Prepare all regulatory information and documentation required to support new or modified products in the region.
- Develop and maintain strong working relationships with regional and global business teams, collaborating closely with R&D, Manufacturing, Procurement, Sales/Marketing, and Regulatory Affairs.
Requisitos
- QUALIFICAÇÕES MÍNIMAS
- Bachelor’s degree completed.
- Experience in Regulatory Affairs within the Personal Care industry.
- Excellent English communication skills, both written and spoken.
- Availability to travel approximately 10% of the time.
- Ability to work on-site in Itupeva, São Paulo, Brazil.
- QUALIFICAÇÕES PREFERENCIAIS
- Experience with ANVISA, IBAMA, and Hazard Communication (GHS/SDS)
- Brazilian Biodiversity, CGen, SisGen, MMA
- Spanish language skills, both written and spoken.
- A proactive mindset, strong interpersonal and communication skills, and the ability to act as a business partner by working closely with the business.
