FDA Regulatory Consultant Needed for Class II Medical Device (Preliminary Advisory Engagement)

Remote Full-time
We are seeking an experienced FDA regulatory consultant with deep expertise in Class II medical devices - particularly those involving light-based technologies (e.g., red light/photobiomodulation) and electromagnetic pulse components. This initial engagement will be a preliminary consulting call to help us: - Understand the regulatory pathway for a new Class II device - Verify assumptions regarding 510(k) strategy, timeline, and cost - Evaluate the regulatory requirements for our device architecture - Determine scope and readiness for a full 510(k) submission - Establish whether you might serve as our long-term regulatory advisor through submission and FDA clearance The underlying application and use-case will be discussed privately after NDA; therefore, this posting deliberately keeps the product description high-level. About the Device (High-Level Only) - Non-invasive, light-based technology using red light and incoherent light - Includes electromagnetic pulse components - Professional-grade device - No drug, no implant, no invasive features Further details will be shared during the call. What We Need From You (Initial Phase): A 1–2 hour paid consultation covering: - Regulatory pathway analysis (including possible predicate devices) - High-level assessment of 510(k) data needs and testing requirements - Expected FDA interactions, timeline, and budget ranges including your consulting - Recommended next steps to move efficiently toward clearance - Identification of gaps or risks we should account for early Future Scope (Optional, Not Required for Initial Engagement) Based on the outcome of the preliminary consultation, we may expand the engagement to: - Full 510(k) project management and authoring - FDA pre-submission (Q-Sub) and reviewer interaction - End-to-end regulatory strategy through final clearance What to Include in Your Proposal - Brief overview of your FDA Class II experience - Example(s) of 510(k) submissions you’ve led (public details only) - Familiarity with devices using light, lasers, LEDs, or EM energy if applicable - Your hourly rate for the preliminary consultation - Availability for an introductory call within the next 1–2 weeks Apply tot his job
Apply Now →

Similar Jobs

VBC Performance Specialist- Remote

Remote

Regulatory Affairs Consultant (part time)-Medical Devices

Remote

Director of Quality and Regulatory Affairs (Remote)

Remote

Regulatory Affairs Consultant - Medical Devices IVD/CDx (home or office based)

Remote

Healthcare Technology Consulting – Regulatory Reporting Lead

Remote

Nutrition & Regulatory Consultant

Remote

Remote Risk Manager- Risk Management & Patient Safety,

Remote

Risk & Quality Performance Manager (Remote)

Remote

Director, Quality Improvement & Risk Management in Wilmington, DE – Westside Family Healthcare Inc – vsmartpros

Remote

Sr. Manager, Risk Management

Remote

[Remote] Research Scientist Intern (TikTok Recommendation-Large Recommender Models) - 2026 Start (PhD)

Remote

Senior SAP CO Business Analyst - Remote or Hybrid

Remote

Executive Assistant, Current Series & Development (FX) Los Angeles, CA, USA

Remote

Experienced Remote Data Entry Specialist – Amazon Ecommerce Operations with blithequark: Part-Time Opportunity for Detail-Oriented and Self-Motivated Individuals

Remote

Remote Telehealth Compact and State Specific - PM- EO

Remote

Apple Data Entry Jobs (Part-Time Remote) - Hiri...

Remote

Experienced Data Entry Operator – Detail-Oriented and Organized Professional for Accurate Data Management and Team Collaboration

Remote

HIS Operational SME

Remote

**Experienced Customer Care Representative - Delivering Exceptional Service from the Comfort of Your Own Home**

Remote

**Experienced Remote Customer Service Representative - Deliver Exceptional Support Experience to Diverse Client Base**

Remote
← Back