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Global Regulatory Specialist
2 weeks ago
This role involves working on international regulatory affairs, handling dossier preparation for Class I and II products. The ideal candidate will have a strong background in biomedical engineering and at least 6 years of experience in regulatory affairs.
">- Key Responsibilities:
- Be recognized as a key talent in international regulatory filings and procedures
- Centralize regulatory operations to enhance compliance, efficiency, and global market readiness
About Us
We are a health technology company that believes every human matters. We work towards making quality healthcare accessible to everyone.
What We Offer
We provide opportunities for professional growth and development. Our teams collaborate effectively, and we prioritize teamwork and communication skills.
Your Role in Our Team
You will be an impactful member of our Regulatory Affairs team, trusted by management as an independent regulatory team member. You will assist in building a center of excellence for RA operations and enable regulatory compliance in various markets.
