[Hiring] MedTech Subject Matter Expert – Edge AI & Connectivity Platform @Codvo.ai

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Role Description

We are seeking a highly experienced MedTech Subject Matter Expert (SME) to lead domain strategy, compliance alignment, and clinical relevance for a next-generation Edge AI & Connectivity Platform. This role is critical to ensuring that the solution aligns with healthcare regulatory requirements, clinical workflows, and emerging standards in connected diagnostics, real-time patient monitoring, and intelligent medical devices.
• Serve as the MedTech domain authority across platform design, development, and validation activities.
• Translate clinical, regulatory, and business requirements into platform architecture guidance, user needs, and technical features.
• Ensure end-to-end alignment with global MedTech standards including:
• FDA 510(k) submission requirements
• HIPAA and data privacy laws
• EU MDR and ISO 13485 QMS
• IEC 62304 for medical device software
• Review technical design documents, requirement specifications, and validation protocols to ensure regulatory readiness.
• Work with solution architects to validate use cases such as remote patient monitoring, connected diagnostics, and real-time health telemetry.
• Collaborate with product and engineering teams to define edge-to-cloud data flows, security models, and interoperability using HL7, FHIR, and DICOM standards.
• Lead compliance documentation for V&V (Verification & Validation), audit support, and risk management (ISO 14971).
• Participate in client-facing workshops, roadmap planning sessions, and technical presentations to drive stakeholder buy-in.
• Stay updated on innovations and trends in Digital Health, Real-time AI/ML in MedTech, Device Interoperability, and emerging FDA guidance.

Qualifications
• 10–18 years of experience in the Medical Device or Digital Health industry, preferably with exposure to edge, IoT, or AI-based solutions.
• Proven track record of working on regulated healthcare products (Class I, II, or III medical devices).
• Deep understanding of clinical workflows, device lifecycle management, and digital transformation within hospitals or diagnostics labs.
• Prior experience working on product submissions to FDA, CE, or other regulatory authorities.
• Strong grasp of software design controls, clinical risk management, usability engineering, and medical data privacy.

Requirements
• Medical device software development lifecycle (IEC 62304)
• Quality management systems (ISO 13485)
• Risk management standards (ISO 14971)
• Data privacy & security regulations (HIPAA, GDPR)
• FDA regulatory pathways (e.g., 510(k), De Novo)
• EU MDR guidelines and documentation requirements
• Medical interoperability protocols: HL7, FHIR, DICOM

Preferred Skills & Certifications
• RAC Certification (Regulatory Affairs Certification)
• Certified HIPAA Professional (CHP)
• Biomedical Engineering, Clinical Informatics, or HealthTech Product Development background
• Experience working with cloud-to-edge data platforms (e.g., Azure IoT, GCP Edge, AWS Greengrass)
• Familiarity with cybersecurity for medical devices (e.g., FDA Pre-market Guidance for Cybersecurity)

Stakeholder Engagement & Communication
• Comfortable presenting complex regulatory and clinical content to technical and non-technical stakeholders.
• Prior experience leading workshops, requirement elicitation sessions, and technical steering committees.
• Ability to work closely with product managers, clinical advisors, embedded engineers, and cloud/AI architects.
• Strong documentation and writing skills for review of QMS documentation, SoPs, and V&V reports.

Why Join This Project

You’ll be the face of MedTech strategy for a cutting-edge connected healthcare platform designed to reshape patient outcomes and real-time diagnostics. This is an opportunity to work at the intersection of regulatory science, clinical innovation, and applied AI backed by a global delivery team with strong engineering depth and execution maturity.