💼 About This Role

You'll manage regulatory submissions for a major consumer products client, ensuring timely approvals and renewals. You'll collaborate with cross-functional teams and government agencies to support business plans. This hybrid role offers career growth within a global CRO.

🎯 What You'll Do

• Prepare and submit regulatory dossiers for new registrations and changes.
• Coordinate with stakeholders to obtain documentation and manage submissions.
• Review labels and ensure compliance with local regulations.
• Support audits and maintain records of regulatory activities.

📋 Requirements

• 1-2 years of experience in regulatory environment.
• Bachelor's degree in Engineering, Pharmacy, or life science.
• Fluent in Portuguese and advanced English reading/writing.
• Experience preparing submissions for Brazilian Health Authorities.

✨ Nice to Have

• Medical devices or pharma background.
• Project management skills and Excel proficiency.
• Intermediate to advanced English speaking.

🎁 Benefits & Perks

• 🏖️ Hybrid work - 3 days remote per week.
• 📈 Career development opportunities in global CRO.
• 🔄 12-month contract with potential renewable.

📨 Hiring Process

Estimated timeline: 2-3 weeks · AI estimate

1. 1Recruiter Call· 30 min
2. 2Hiring Manager Interview· 60 min
3. 3Offer· 1 week