Related skills
english portuguese medical devices pharma gmp📋 Description
- Ensures submissions for market licenses, changes, renewals, and registrations.
- Coordinate establishment registrations and related regulatory activities.
- Balance multiple projects and interact with stakeholders.
- Support audits and post-approval activities.
🎯 Requirements
- 1-2 years regulatory experience; submissions for Brazilian Health Authorities; track record.
- Desirable: Medical Devices or Pharma background.
- Bachelor's degree in Engineering, Pharmacy, or life sciences. Proficient in English; fluent in Portuguese.
- Excel proficiency for data management.
🎁 Benefits
- Hybrid work arrangement with a major consumer products client.
- Contract role (12 months) with renewal option.
- Global CRO focused on quality and development.
- Strong training and career development culture.
- Diverse and inclusive workplace.
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