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

[Remote] HRIS & Payroll Specialist (Remote in CST or EST)

Remote Full-time

Experienced Senior Analyst, Contract Management – 340B Program Operations and Negotiations Specialist

Remote Full-time

Part Time Triage Nurse – Remote, KY

Remote Full-time

Experienced Remote Data Entry Specialist – Flexible Part-Time Work from Home Opportunity with arenaflex

Remote Full-time

Experienced Customer Service and Inside Sales Representative for a Dynamic Food Distribution Company - arenaflex

Remote Full-time

Mainframe Systems Programming - CICS

Remote Full-time

Experienced Remote Data Entry Specialist - Join Blithequark's Dynamic Team and Bring Magic to Life from the Comfort of Your Home

Remote Full-time

Experienced Remote Data Entry Clerk and Administrative Support Specialist for Part-Time Opportunity with blithequark

Remote Full-time

Office Manager/Accounting & Project Manager

Remote Full-time

[Remote] Corporate Video Editor

Remote Full-time
← Back to Home