Compliance SME – Medical Device Software (Remote)

Remote, USA Full-time
Job Description: Compliance SME – Medical Device Software Department: Regulatory & Quality Assurance Role Overview: We are seeking a highly skilled and detail-oriented Compliance Subject Matter Expert (SME) to lead and support regulatory compliance initiatives for medical device software. The ideal candidate will have deep expertise in global regulatory frameworks, quality management systems, and risk management practices applicable to software as a medical device (SaMD). Key Responsibilities: Regulatory Strategy & Engagement: • Lead classification and regulatory pathway analysis for SaMD under FDA guidelines, including 510(k) submissions. • Facilitate early engagement with FDA through pre-submission meetings. Quality Management System (QMS): • Implement and maintain QMS in accordance with ISO 13485:2016. • Oversee document control, change management, and supplier qualification processes. • Ensure integration of risk management into QMS activities. Software Lifecycle Compliance: • Ensure software development processes align with IEC 62304 standards. • Manage software safety classification (Class B or higher). • Oversee development planning, requirements analysis, design, implementation, verification, validation, and release. Risk Management: • Apply ISO 14971 principles to identify, evaluate, and mitigate risks throughout the product lifecycle. • Collaborate with cross-functional teams to ensure risk controls are effectively implemented and documented. Required Qualifications: • Bachelor's or Master’s degree in Engineering, Life Sciences, or related field. • 7+ years of experience in regulatory compliance for medical devices or SaMD. • Proven expertise in FDA regulations, ISO 13485, IEC 62304, and ISO 14971. • Strong understanding of software development and validation processes. • Excellent communication and documentation skills. Preferred Qualifications: • Experience with international regulatory bodies (e.g., EU MDR, Health Canada). • Certification in Regulatory Affairs or Quality Management. • Familiarity with digital health technologies and AI/ML in medical devices. What We Offer: • Opportunity to work on cutting-edge medical technologies. • Collaborative and inclusive work environment. • Competitive compensation and benefits. Apply tot his job
Apply Now

Similar Jobs

Regulatory Counsel

Remote, USA Full-time

[Remote] U.S. Cybersecurity Policy Consultant – Federal Regulation Advisory Role (Hourly or Project)

Remote, USA Full-time

Electric Compliance & Risk Consultant, Senior

Remote, USA Full-time

Regulatory Submission Associate III - Remote (Part-Time)

Remote, USA Full-time

[Remote] Regulatory Consultant CMC - Small Molecule

Remote, USA Full-time

POLICE DEPARTMENT – Communications Operator (911 Dispatcher)

Remote, USA Full-time

Accounts Payable Clerk job at Astrix Technology Group in New Brunswick, NJ

Remote, USA Full-time

Coordinator, Sales & Artistry - Austin

Remote, USA Full-time

Assistant Farm Coordinator - Yapahnk, NY

Remote, USA Full-time

North America Retail Positions Sign-Up

Remote, USA Full-time

Remote Healthcare Consultant Jobs In New York

Remote, USA Full-time

Technical Account Manager (Partner Integrations) with BI (MySQL & Tableau/Looker)

Remote, USA Full-time

Amazon Delivery Station Warehouse Associate Rem...

Remote, USA Full-time

**Experienced Customer Engagement Associate – Global Customer Service and Support**

Remote, USA Full-time

Legal Assistant- NOT REMOTE

Remote, USA Full-time

Part-Time Scientific Research Writer, Nursing Research

Remote, USA Full-time

**Experienced Remote Chat Support Agent – Deliver Exceptional Customer Service from Anywhere, Earning $25-$35/hr**

Remote, USA Full-time

International Tax Accounting Advisor

Remote, USA Full-time

Experienced Remote Data Entry Specialist – Join the Dynamic Team at blithequark and Elevate Your Career in Aviation

Remote, USA Full-time

Sales Associate (Full-Time) - Colony Plaza, Aug...

Remote, USA Full-time
Back to Home