G

GE Healthcare

Imaging, monitoring, and healthcare IT solutions

Lead Specialist - Quality, Digital

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-time

About the Job

Requirements

  • A bachelor's degree in Engineering, Computer Science, Software Engineering, Quality, Life Sciences, or a related technical discipline, or a high school diploma/GED with at least 10 years of relevant experience.
  • At least 6 years of experience in software quality, software engineering, design assurance, quality systems, regulatory compliance, or digital product development.
  • Experience supporting Agile, Scrum, DevOps, DevSecOps, or similar software-development methodologies.
  • Knowledge of software lifecycle principles, including requirements, design, development, verification, validation, configuration management, release management, and change control.
  • Experience translating quality-system requirements into practical processes for product and engineering teams.
  • Technical writing, documentation review, analytical, problem-solving, and communication skills.
  • Ability to work independently, exercise sound judgment, and identify when escalation or additional expertise is needed.
  • Must be legally authorized to work in the United States.

Responsibilities

  • Provide quality guidance throughout product development, release, deployment, maintenance, change, and retirement activities.
  • Support non-medical-device software, SaaS, cloud applications, digital platforms, APIs, reusable components, and software services used by or integrated with regulated medical-device products.
  • Evaluate product intended use, software boundaries, and risk to determine appropriate quality, regulatory, lifecycle, design control, and documentation requirements.
  • Provide oversight of software lifecycle activities, including requirements, design, development, verification, validation, release readiness, configuration management, and change control.
  • Review lifecycle and quality documentation for completeness, consistency, traceability, objective evidence, and compliance.
  • Partner with product and engineering teams to implement scalable quality practices within Agile, DevSecOps, cloud, and continuous-delivery environments.
  • Support software, cybersecurity, operational, data, integration, supplier, and component risk-management activities.
  • Participate in design, technical, release-readiness, change-control, and lifecycle milestone reviews as the Quality representative.
  • Develop and improve procedures, work instructions, templates, training materials, checklists, and quality records.
  • Identify opportunities to simplify, standardize, and automate quality processes and integrate compliance into development workflows.
  • Train and coach cross-functional teams on software lifecycle, documentation, risk management, verification and validation, and QMS expectations.
  • Develop and monitor quality metrics and leading indicators to identify trends, risks, and improvement opportunities.
  • Support investigations, CAPAs, audits, inspections, and other quality-system activities.
  • Collaborate across functions to resolve complex software quality issues and establish sustainable solutions.
  • Monitor evolving software, cloud, digital health, AI, cybersecurity, and quality-system requirements and assess their applicability.
  • Promote a quality culture focused on prevention, accountability, continuous improvement, and efficient compliance.

Desired Qualifications

  • Experience in medical devices, healthcare technology, digital health, or another regulated software environment.
  • Experience supporting both regulated medical-device software and non-medical-device software.
  • Experience with cloud-native applications, SaaS, APIs, microservices, reusable components, or software platforms.
  • Familiarity with applicable standards and regulations, including ISO 13485, IEC 62304, ISO 14971, IEC 82304-1, FDA software expectations, cybersecurity requirements, and software-validation principles.
  • Experience with software risk management, design and change control, verification and validation, traceability, supplier or component management, and release readiness.
  • Familiarity with CI/CD pipelines, software repositories, automated testing, and electronic quality evidence.
  • Experience supporting AI/ML-enabled software, data platforms, or cloud-based healthcare applications.
  • Experience developing procedures, templates, training, quality records, or process improvements.
  • Project-management and stakeholder-influencing skills.

About the Company

GE Healthcare

Imaging, monitoring, and healthcare IT solutions

GE Healthcare Systems provides medical technologies and digital infrastructure to improve diagnosis, treatment, and monitoring of patients. Its products include imaging systems (radiology and cardiology), mobile diagnostic tools, patient monitoring devices, and healthcare IT software that combine hardware, software, and services sold to hospitals, clinics, and research institutions, with revenue from device sales, software licenses, and long-term service contracts. The company differentiates itself by offering a wide, integrated ecosystem of hardware, software, and services, plus AI-driven analytics and a global service network supported by substantial R&D investment. Its goal is to improve patient outcomes and healthcare efficiency by delivering reliable imaging, diagnostics, monitoring, and IT solutions for clinicians.

Company size
1-10
Company stage
IPO
Headquarters
Chicago, IL
Founded
1892

Recently Posted Jobs

Explore more opportunities at GE Healthcare

See more jobs