Compliance SME – Medical Device Software (Remote)

Remote 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 Full-time

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

Remote Full-time

Electric Compliance & Risk Consultant, Senior

Remote Full-time

Regulatory Submission Associate III - Remote (Part-Time)

Remote Full-time

[Remote] Regulatory Consultant CMC - Small Molecule

Remote Full-time

POLICE DEPARTMENT – Communications Operator (911 Dispatcher)

Remote Full-time

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

Remote Full-time

Coordinator, Sales & Artistry - Austin

Remote Full-time

Assistant Farm Coordinator - Yapahnk, NY

Remote Full-time

North America Retail Positions Sign-Up

Remote Full-time

Sourcer *REMOTE

Remote Full-time

Delta Airlines (Data Entry) Work From Home Position Jobs - Apply Now

Remote Full-time

Associate Counsel - Remote (CA, WA, OR, MT, NM, AK, TX)

Remote Full-time

Leader of Financial Planning & Analysis (Remote - NC, Research Triangle & Boston)

Remote Full-time

**Experienced Data Entry Research Panelist – Flexible Remote Work Opportunity at blithequark**

Remote Full-time

**Experienced Part-Time Remote Data Entry Specialist – Healthcare Industry Support**

Remote Full-time

Python Developer Needed to Debug & Stabilize Slide Generator Pipeline (DOCX → JSON → HTML → PDF) - Contract to Hire

Remote Full-time

Career with American Airlines:Flight Attendant | Hiring

Remote Full-time

Experienced Data Entry Professional - Work from Home Opportunity at blithequark

Remote Full-time

Experienced Customer Service Professional – Remote Customer Assistance Agent with Competitive Pay and Flexible Scheduling at arenaflex

Remote Full-time
← Back to Home