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Overjet

AI platform for dental clinical care

Head of Regulatory

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeSan Mateo, CA, USA

About the Job

Requirements

  • At least 7 years of experience in medical-device regulatory affairs, including at least 2 years working with software as a medical device under FDA and at least one international regulatory framework such as Health Canada, EU MDR, MHRA, or TGA.
  • Proven success managing regulatory submissions and approvals in multiple jurisdictions, such as FDA 510(k), De Novo, CE Marking, MDEL, UK MHRA registration, and TGA conformity assessments.
  • Deep knowledge of U.S. FDA regulations, including 21 CFR Part 820 and SaMD guidance; Canada's Medical Devices Regulations; EU MDR and IVDR, including Notified Body processes; UK Medical Device Regulations; and Australian TGA requirements, including the sponsor model.
  • Experience interacting directly with agencies and Notified Bodies, including leading meetings and responding to questions or deficiencies.
  • Expertise in ISO 13485, ISO 14971, and IEC 62304.
  • Strong knowledge of quality management systems and compliance audits, including internal and external inspection readiness.
  • Ability to translate technical and regulatory language for cross-functional teams.
  • Bachelor's degree in a scientific or engineering discipline.
  • High degree of ownership, self-direction, and comfort working in fast-paced, high-growth environments.

Responsibilities

  • Develop, lead, and execute the company's global regulatory strategy, ensuring alignment with business goals and evolving international requirements.
  • Own planning, coordination, and submission of regulatory filings, including FDA 510(k), De Novo, Health Canada Medical Device License (MDL), EU MDR through SGS Notified Body and Casus EU Responsible Person, UK MHRA registration through Casus UK Responsible Person, and Australian TGA through sponsor Emergo by UL.
  • Serve as the primary point of contact with regulatory authorities, including FDA, Health Canada, MHRA, TGA, and EU Notified Bodies, for product approvals, quality management system compliance, and ongoing reporting.
  • Interpret and communicate new or evolving global regulatory requirements across internal stakeholders, and incorporate them into the company's regulatory and quality systems.
  • Partner with Product, Clinical, Engineering, and QA teams to embed regulatory requirements throughout the product lifecycle, including design controls, validation, verification, and risk management.
  • Manage development and maintenance of submission-ready documentation and regulatory dossiers.
  • Provide regulatory input for clinical studies, real-world evidence programs, and data usage strategies.
  • Collaborate with the VP of Machine Learning & Compliance and Director of Security to align regulatory strategies with privacy, cybersecurity, and AI risk management frameworks.
  • Support regulatory due diligence for partnerships, audits, and customer-facing compliance engagements.
  • Lead inspections and audits from regulatory authorities and Notified Bodies, and ensure timely resolution of findings.
  • Build and manage the regulatory team as the company scales globally.

Desired Qualifications

  • Advanced degree, such as an MS, PhD, JD, or MPH, or RAC credential.
  • Familiarity with ISO 27001 and data protection standards such as HIPAA and GDPR.

About the Company

Overjet

AI platform for dental clinical care

Overjet provides AI-powered tools for dentistry with two platforms: Clinical Intelligence for providers and Claim Intelligence for payers. The Clinical platform combines AI analysis of dental radiographs with practice data to help clinicians improve precision, efficiency, training, and patient outcomes. The Claim platform analyzes radiographic claims and related data to speed up reviews and allow AI-confirmed claims to be approved quickly while human reviewers focus on the most important cases. By focusing on dentistry and serving both providers and payers with tailored, end-to-end solutions, its goal is to make dental care more precise, efficient, and patient-centered through AI-assisted care and streamlined claims processing.

Company size
201-500
Company stage
Series C
Total funding
$130.6M
Headquarters
Cambridge, MA
Founded
2018

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