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Regulatory Specialist II
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- This position is a one year contract with the possibility of extension or conversion to permanent.
- 5+ years of regulatory affairs experience
- Medical Device regulatory affairs experience
- Understand country-specific requirements and deliver those to internal stakeholders, including product management, engineering, labeling, etc., for product registration and change planning.
- Communicate weekly with affiliate RAs in different time zones to catch up on ongoing projects and discuss the issues to solve.
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