About this opportunity
LHH lists this Senior Regulatory Affairs Lead - Medical Devices (510(k)/EU MDR) opportunity in dublin, California. Review the employer’s description below for duties, qualifications and application requirements.
Job description
LHH is seeking a Senior Regulatory Affairs Specialist in Dublin, California to support global regulatory strategies for medical devices. The role involves preparing submissions, leading communications with regulatory agencies, and ensuring compliance with evolving regulations.
The ideal candidate has over 8 years of experience in regulatory affairs, particularly with FDA 510(k) and EU MDR submissions. Strong project management and technical writing skills are essential.
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Worksite address
dublin, CA, 94568, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.