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Job description
A leading medical technology firm is seeking a Regulatory Affairs professional to develop and execute regulatory strategies for innovative medical devices. The ideal candidate will have 8-10 years of experience in US and/or EU regulatory affairs, particularly in Software as a Medical Device (SaMD). This full-time position offers a competitive salary package and excellent benefits including medical, dental, vision insurance, and a 401(k) plan with company match. This position is remote, allowing flexibility in managing work-life balance.
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Worksite address
san francisco, CA, 94199, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.