Regulatory Affairs Specialist
Há 3 dias
We are seeking a highly skilled Regulatory Affairs Specialist to join our team at Sewell Lincoln. This role will be responsible for coordinating and submitting new drug / medical devices applications to regulatory agencies in Brazil.
Key Responsibilities:
- Plan, conduct and coordinate JJV regulatory activities for Brazil, ensuring compliance with all relevant regulations.
- In partnership with RA management, establish and execute Brazil regulatory strategies for new and existing products, driving business growth and success.
- Diligently research and analyze regulatory requirements, providing expert guidance to ensure seamless product approvals.
The ideal candidate will possess excellent communication and problem-solving skills, with the ability to work effectively in a fast-paced environment. A strong understanding of Brazilian regulatory frameworks and procedures is essential.
Requirements- Bachelor's degree in Life Sciences, Pharmacy, or a related field.
- Minimum 3 years of experience in regulatory affairs, preferably in the pharmaceutical industry.
- Excellent knowledge of Brazilian regulatory agencies and procedures.
- Strong analytical and problem-solving skills.
- Effective communication and collaboration skills.
As a Regulatory Affairs Specialist at Sewell Lincoln, you can expect a competitive salary package, including:
- Salary: $80,000 - $100,000 per year (depending on experience).
- A comprehensive benefits package, including health insurance, retirement plan, and paid time off.
- Ongoing training and professional development opportunities.
- A dynamic and supportive work environment.
Sewell Lincoln is a leading automotive group dedicated to delivering exceptional customer experiences. Our team is passionate about innovation, excellence, and community involvement. If you're a motivated and detail-oriented individual who shares our values, we encourage you to apply for this exciting opportunity.
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