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Director of Regulatory and QA - Medical Device

NPA WorldWide
Cambridge, Massachusetts, USA
$200K-$240K a year
Permanent
Full-time

Job description : *Director of Regulatory Affairs & Quality Assurance (RA / QA)*We're working closely with the C-suite at an exciting medical-device company to recruit a Director of Regulatory Affairs & Quality Assurance, who will lead the development and execution of comprehensive regulatory and quality systems.

This role is pivotal in both securing immediate FDA 510(k) approval for next-generation products and laying the groundwork for scalable operations that will support future growth.

What You'll Do : - Own the regulatory function, including managing a small regulatory team.- Lead efforts to obtain FDA 510(k) clearance, working closely with internal teams and external partners.

  • Design and execute clinical validation studies.- Build and implement quality assurance systems from the ground up.- Ensure compliance with US and global regulatory standards, including European regulations.
  • Collaborate with internal stakeholders and external clinicians at major US medical facilities.- Work in a flexible, hands-on environment where you will create and implement new processes.

Qualifications : What Youll Need : - Proven experience with FDA 510(k) submissions and medical device regulatory requirements.

  • Strong background in both hardware and software regulatory affairs and quality assurance.- Experience designing and executing clinical validation studies.
  • Ability to build scalable regulatory and quality systems from scratch.- Experience leading and mentoring a regulatory team.
  • Practical, hands-on approach and a startup mentalitycomfortable working in an evolving environment.- Strong collaboration skills and the ability to work closely with cross-functional teams, customers, and clinicians.
  • Must be based in the Boston area or within a 2-3 hour drive, with the ability to come to the office regularly. Why is This a Great Opportunity : Why Youll Want to Join : - Be a key leader in driving regulatory and quality systems for an innovative medical device company.
  • Hands-on role with significant impact on long-term growth and compliance.- Competitive compensation up to $240K plus stock options.
  • Collaborate with diverse teams across the US and internationally.- Flexible, startup-like environment where you can make a real difference.
  • Salary Type * : Annual Salary*Salary Min * : $ 200000*Salary Max * : $ 240000*Currency Type * : USD
  • 9 days ago
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