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Regulatory Affairs Specialist (Medical Device)
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- Regulatory Affairs Specialist (Medical Device)
- Regulatory Affairs/Medical Device experience (1-2 years)
- The Regulatory Affairs Specialist - Contractor will assist with a variety of regulatory tasks in support of global regulatory strategy, regulatory assessment for modified product, regulatory filing for new/modified product, regulatory operation and processes, post-market surveillance.
- Assist in post-market surveillance activities, such as complaint handling and vigilance reporting
- Assist in regulatory involved QMS activities, such as CAPA, Non-Conformance
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