Regulatory Affairs Analyst – Mid-level

Jobtailor; Embu-Guaçu; Presencial; BRL 60 000 - 90 000; Tempo integral

Resumo da oferta

Jobtailor is seeking a Regulatory Affairs Specialist to oversee product regularization and registration before ANVISA and other authorities. You will ensure labeling and ingredient compliance, perform regulatory assessments, and support internal teams with technical regulatory guidance.

Responsibilities include monitoring inspections, preparing documentation, and participating in regulatory projects to adapt to evolving legislation.

Qualificações

• Regulatory knowledge applicable to health/sanitary regulations.
• Ability to prepare and review regulatory documents and labeling.
• Experience supporting internal teams (R&D, Marketing, Quality, Supply, Commercial).
• Familiarity with ANVISA systems and international standards is desirable.

Responsabilidades

• Prepares labeling and regulatory assessments; manages notifications and registrations.
• Provides technical support to R&D, Marketing, Quality, Supply and Commercial teams.
• Monitors inspections and prepares regulatory documentation.
• Participates in regulatory projects and tracks legislative changes.

Conhecimentos

Regulatory interpretation

Technical writing

Formação académica

Degree in Pharmacy, Chemistry, Biomedicine, Nutrition or related fields

Ferramentas

Solicita

SEI

Datavisa

Descrição da oferta de emprego

• Responsible for conducting product regularization and registration processes before ANVISA and other competent authorities, ensuring compliance with applicable legislation, particularly relating to dietary supplements, ingredients and labeling.
• Prepares and reviews labeling, performs regulatory compliance assessments, manages notifications and registrations, analyzes legislation, provides technical support to internal areas (R&D, Marketing, Quality, Supply and Commercial), monitors inspections and prepares technical and regulatory documentation.
• Participates in the implementation of regulatory projects and in monitoring changes in legislation, ensuring the ongoing compliance of products and processes.

Requirements

• Previous experience in the role
• Experience interpreting and applying sanitary/health regulations
• Degree in Pharmacy, Chemistry, Biomedicine, Nutrition or related fields
• Experience with ANVISA systems (Solicita, SEI, Datavisa) and familiarity with international standards (Codex, FDA) is desirable.