Regulatory Affairs Analyst – Mid-level

BRG

Regulatory Affairs Analyst ensuring compliance with ANVISA regulations at BRG Suplementos Nutricionais. Collaborating with various internal teams on product regularization processes.

Posted 7/4/2026full-timeEmbu-Guaçu • 🇧🇷 BrazilMid-LevelSeniorWebsite

About the role

Key responsibilities & impact

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

What you’ll need

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.

Benefits

Comp & perks

Hybrid model (3 days in the office and 2 days remote)
On-site cafeteria
On-site parking
Meal voucher and/or grocery allowance
Health and dental insurance
Pharmacy partnership
Group life insurance
Transportation voucher or mobility allowance
Profit sharing (PLR)
Gympass
Discount on brand products

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

Regulatory Compliance AssessmentsLabeling Preparation and ReviewLegislation AnalysisTechnical SupportProduct Registration Processes