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Job description
Johnson & Johnson is seeking a Senior Regulatory Affairs Program Lead to drive regulatory strategy and execution for the OTTAVA robotics portfolio, collaborating closely with engineering and clinical teams. The role focuses on US and international submissions, including FDA filings, to enable timely market access.
The candidate will work across global health authorities, coordinate with product development, and support strategic regulatory initiatives, with up to 25% travel.
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Worksite address
cincinnati, OH, 45208, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.