Pulpdent Corporation in Watertown, MA, seeks a Head of Regulatory Affairs to guide global regulatory strategy across R&D, manufacturing, and marketing. Lead a high-performing team, manage FDA submissions, and ensure compliance with EU MDR and ISO 13485.
This on-site role partners with R&D, quality, and operations to enable safe, compliant products worldwide. The ideal candidate has 10+ years in medical devices regulatory affairs, a strong leadership track record, and deep knowledge of

#J-18808-Ljbffr Pulpdent-Corporation