Hybrid Regulatory Affairs Specialist / Manager, CDx

Posted 5 hours ago

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About the role

  • Regulatory Affairs Specialist managing FDA submissions for innovative medical diagnostics. Drive regulatory strategies and collaborate with teams to ensure compliance and approvals.

Responsibilities

  • Provide strategic and operational regulatory support for diagnostic and CDx products, including software-based and other complex IVD medical devices.
  • Drive and coordinate the development and execution of US FDA and global regulatory strategies and submission plans (e.g. Q-Subs, 510(k), PMA, and equivalent pathways) to support timely product clearances and approvals.
  • Contribute to the drafting, review, and compilation of regulatory submissions and responses, collaborating closely with clinical, quality, R&D, and commercial teams.
  • Support interactions with regulatory authorities (e.g. FDA and other key agencies) and act as a central point of contact for CDx/IVD regulatory topics across internal stakeholders.

Requirements

  • 5-8 years' Regulatory Affairs experience within Diagnostics and/or Medical Devices (complex Class II / Class III)
  • Practical experience contributing to FDA submissions for diagnostic and/or software medical devices (e.g. Q-Subs, 510(k), De Novo, PMA or supplements), with tangible involvement in drafting or compiling submission content
  • Background in diagnostics (CDx and/or broader IVD) with an understanding of NGS and/or software as a medical device highly beneficial
  • Experience interacting with Health Authorities (e.g. FDA) essential; exposure to additional global agencies (e.g. Health Canada, TGA, PMDA or EU Notified Bodies) highly beneficial
  • Familiarity with global regulatory requirements for diagnostics and an interest in expanding knowledge into new regions and evolving frameworks
  • Must be fluent in English.

Benefits

  • Outstanding Medical, Dental & Vision with 90% Employer Contribution
  • Company matched 401K at 4%
  • Company-paid short & long-term disability insurance
  • FSA commuter benefits
  • 20 Days PTO, increasing to 25 with tenure; 5 Days Sick and 14 Public Holidays
  • Free EAP

Job title

Regulatory Affairs Specialist / Manager, CDx

Job type

Experience level

Mid levelSenior

Salary

$71,000 - $143,000 per year

Degree requirement

Bachelor's Degree

Location requirements

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