Sonova·13 days ago
13 days ago
Senior Specialist, International (China) Regulatory Affairs
Sign up free to see how well your resume matches this role.
What you'll do
- Supporting regulatory activities for Class III medical devices in China and Taiwan
- Preparing regulatory submissions
- Ensuring compliance
What they're looking for
- Significant experience in medical device regulatory affairs
Summarised by NextRaise from the employer’s description, which follows in full below.
Full description from employer
Become part of our team as a Senior Specialist, International (China) Regulatory Affairs, supporting regulatory activities for Class III medical devices in China and Taiwan. Key responsibilities include preparing regulatory submissions and ensuring compliance. Ideal for candidates with significant experience in medical device regulatory affairs.
Skills
- regulatory affairs
- medical device regulatory compliance
- china regulatory requirements
- taiwan regulatory requirements
- regulatory submissions
- product technical documentation
- sop development
- process improvement
- regulatory impact assessment
- product access management
- regulatory information management systems
- sap
- microsoft office
- data management
- documentation organization
- english
- agile plm
- proofreading
- problem solving
- writing
- remote work technology
Company
Sonova
city, United States of America
Company facts come from this company's own listings. We only show what the postings themselves carry.