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SHL Senior Regulatory Affairs Specialist

Job Description

Mission/Position Headline:       

Fast and efficient registration for responsible products and contribute the time to market.

Areas of Responsibilities:           

  • Monitor the change of regulation, technical requirements and standards timely and adapt into product registration.
  • Maintain or develop good working relationship and cooperation with relevant authorities like test labs, CMDE etc. to improve working efficiency;
  • Provide regulatory support on both pre-market and post-market issues on responsible product lines.
   

Requirements:

  • Bachelor’s degree or above relevant in medical/ biological/engineering etc.
  • Above 2 years in regulatory affairs of active medical device, RA experience on image systems is priority.
  • Experience in active medical device industry, include but not limited to product registration, R&D, clinical etc.
  • Good coordination and communication skills and teamwork spirit.

Organization: Siemens Healthineers

Company: Siemens Healthineers Ltd.

Experience Level: Experienced Professional

Job Type: Full-time

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