Principal Regulatory Affairs Specialist job
Medical Device Company - Eden Prairie, MN
Direct hire - salary up to $130K + bonus
As the Principal Regulatory Affairs Specialist you will work on electro-mechanical medical devices, where you will you be responsible for global regulatory affairs strategy including authoring 510K submissions and interacting directly with the FDA.
You will lead cross functional interactions with product development, sales, marketing and all other core teams to manage the full product life cycle.
The ideal candidate must have 7 years of regulatory affairs experience in the medical device industry and have experience authoring 510K submissions.
If you are interested in finding out more about this opportunity please apply with your resume.
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