Regulatory Affairs Specialist for Pharmaceutical Products
1 dia atrás
Sully's Steamers Johnson City seeks a highly skilled Regulatory Affairs Specialist to coordinate, compile and submit new drug/medical devices applications to regulatory agencies in Brazil.
The ideal candidate will plan, conduct and coordinate JJV regulatory activities for Brazil, working closely with RA management to establish and execute regulatory strategies for new and existing products. Additionally, they will collaborate with cross-functional teams to ensure regulatory compliance and be responsible for coordinating and submitting regulatory documents to regulatory agencies.
Key Responsibilities- Regulatory Planning: Develop and implement regulatory plans to ensure timely submissions and approvals of pharmaceutical products in Brazil.
- Regulatory Strategy Development: Collaborate with RA management to develop and execute regulatory strategies for new and existing products in Brazil.
- Document Submission: Coordinate and submit regulatory documents to regulatory agencies in Brazil, ensuring accuracy and completeness.
- Team Collaboration: Work closely with cross-functional teams to ensure regulatory compliance and coordination.
About the Role:
- This is a full-time position offering an estimated salary range of $80,000 - $110,000 per year, depending on experience.
- The successful candidate will have excellent communication and project management skills, as well as a strong understanding of Brazilian regulatory requirements.
- If you are a motivated and organized individual with a passion for regulatory affairs, we encourage you to apply.
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