1. Main Responsibility:
-- Involve CT R&D related S&L implementation, from system to component.
-- System/component level IEC and EMC evaluation, testing and evidence.
-- CFDA registration task: PTR responsible, safety & performance testing, EMC testing.
-- Plan for regulatory related testing and make alignment with project milestone.
-- Coordinate internal and external resource for regulatory related task.
-- Support country registration regulatory testing part.
-- Cooperation with Germany CT SE Approval team for global approval topics.
-- Join the IEC/China standard committee activity for standards updating and drafting.
2. Education and Experience
-- Experience with medical equipment regulatory, or 3rd party regulatory is preferred.
-- Bachelor’s degree or above

Organization: Siemens Healthineers

Company: Siemens Shanghai Medical Equipment Ltd.

Experience Level: Mid-level Professional

Job Type: Full-time