Industry / Sector / Domain
Medical Devices
Location
Beijing, China
Experience Range
2-10 years
Company Profile
A leading multinational company in the medical devices domain
Job Profile
- Responsible for the registration of products and the service of the company in the region
- Execute regulatory plans for complex projects including new products, renewal and modification for existing marketing authorizations
- Draft product standard according to internal specification and regional standards
- Maintain, update and archive the submission sets together with approved product documents
- Perform gap analysis on regulatory requirements and propose solutions
Candidate Profile
- Working knowledge of healthcare along with experience of registration and regulatory affairs in the Medical Devices Industry
- Familiar with regional medical devices registration, policies and relevant declaration processes
- Excellent communication skills and organizational skills
- Ability to interact with all levels of employees and working closely with colleagues
- Relevant educational qualification with 2 to 10 years of working experience
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