Lead Specialist, Quality, Digital
$106.4k - $159.6kGE Healthcare
Job Description Summary
The Lead Specialist Digital Quality provides quality leadership and technical expertise for software products cloud-based solutions digital platforms and software services developed within the Pacific Northwest Science & Technology Organization. This role partners with Product Engineering Regulatory Cybersecurity Privacy Data/AI and Quality teams to establish practical risk-based controls throughout the software lifecycle. The Lead Specialist serves as a trusted advisor translating Quality Management System requirements into scalable and efficient development practices.Job Description
Roles and 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 the 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.
Required Qualifications
- Bachelors 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.
- 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.
- Strong 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.
Desired Characteristics
- 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.
- Strong project-management and stakeholder-influencing skills.
Additional Information
GE HealthCare offers a great work environment professional development challenging careers and competitive compensation. GE HealthCare is an Equal Opportunity Employer
GE HealthCare will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a drug screen (as applicable).
While GE HealthCare does not currently require U.S. employees to be vaccinated against COVID-19 some GE HealthCare customers have vaccination mandates that may apply to certain GE HealthCare employees.
Relocation Assistance Provided: No
Required Experience:
IC
$106.4k - $159.6k
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