Global Regulatory Affairs Manager
hace 1 semana
About Us
Smith+Nephew is a leading medical technology company dedicated to helping healthcare professionals restore function and form in patients' lives. We pride ourselves on our commitment to innovation, customer satisfaction, and excellence in all aspects of our business.
Job Summary
We are seeking a highly skilled Regulatory Affairs Specialist II to join our team. The ideal candidate will have a strong background in regulatory affairs, excellent communication skills, and the ability to work effectively in a fast-paced environment.
Main Responsibilities:
- Develop and implement regulatory strategies to ensure compliance with US and global regulatory requirements.
- Prepare international dossiers for EU and global market affiliates.
- Collaborate with cross-functional teams to deliver high-quality regulatory submissions.
- Provide expert advice on regulatory matters to internal stakeholders.
What You'll Need:
- Bachelor's degree in Engineering, Biomedical Science, Pharmacy, Medicine, or a related field.
- 2+ years of experience in the Regulatory Affairs medical device industry.
- Excellent research and analytical skills, with attention to detail.
Why Join Us?
At Smith+Nephew, we're passionate about improving patient outcomes and enhancing the quality of life for individuals around the world. If you share our commitment to excellence and customer satisfaction, we invite you to explore this opportunity further.
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