Industry / Sector / Domain

Medical Devices


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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Personal Details

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