Quality Engineer - SaMD
Remote, United States
The Quality Engineer provides quality engineering process support to GE HealthCare digital products in accordance with GE HealthCare medical device Quality Management System (QMS). They are responsible for the development, implementation, improvement and continuous reinforcement of established Quality Assurance fundamental practices that are utilized in the local business.
GE HealthCare is a leading global medical technology and digital solutions innovator. Our purpose is to create a world where healthcare has no limits. Unlock your ambition, turn ideas into world-changing realities, and join an organization where every voice makes a difference, and every difference builds a healthier world.
Job Description
In this role you will:
- Guide teams in creating software development plans, design change plans, design inputs, verification and validation plans and reports, risk management documentation, defect resolution, SDLC deliverables, design reviews, non-product software validation.
- Participate in core teams as the quality representative, and review and approve program documentation.
- Ensure program compliance to GE work instructions and applicable regulations such as ISO 13485, ISO 14971, IEC 62304, 21 CFR Part 820, MDD, MDR.
- Support nonconformance evaluations, investigations, CAPA action plans, effectiveness checks.
- Participate in internal audits and support internal and external audits.
- Perform other duties as assigned.
Basic Qualifications:
- Bachelor’s degree in engineering, computer science, or equivalent.
- Minimum 3 years’ experience in Quality Assurance/Regulatory Affairs.
- Experience in software within a regulated industry.
- Must be willing to travel as required.
- Legal authorization to work in the U.S. is required. We will not sponsor individuals for employment visas, now or in the future, for this job opening.
Desired Characteristics:
- Practical knowledge of software development and familiarity with Software Development Lifecycle (SDLC), design change and document change control, process verification and validation methodologies, manufacturing/production process control methodologies in medical device or healthcare software development environment.
- Demonstrated experience with Agile/Lean software development methods.
- Previous project management experience.
- Demonstrated understanding of Medical Device QMS requirements and regulatory requirements including but not limited to FDA CFR 21 820 and ISO 13485.
- Demonstrated expertise with effectively communicating within all levels of the organization around concepts of design controls, design verification and validation activities; production & process controls; Corrective & Preventive Action (CAPA), complaints & risk management.
- Experience in a global working environment.
- Experience leading and implementing change. Experience performing internal audits and participating in external audits.
- Demonstrated technical aptitude (i.e. able to read & comprehend technical documentation & execute procedures), global regulatory experience & demonstrated experience interfacing with regulators.
We expect all employees to live and breathe our behaviors: to act with humility and build trust; lead with transparency; deliver with focus, and drive ownership –always with unyielding integrity.
Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you’d expect from an organization with global strength and scale, and you’ll be surrounded by career opportunities in a culture that fosters care, collaboration and support.
For U.S. based positions only, the pay range for this position is $84,800.00-$127,200.00 Annual. It is not typical for an individual to be hired at or near the top of the pay range and compensation decisions are dependent on the facts and circumstances of each case. The specific compensation offered to a candidate may be influenced by a variety of factors including skills, qualifications, experience and location. In addition, this position may also be eligible to earn performance based incentive compensation, which may include cash bonus(es) and/or long term incentives (LTI). GE HealthCare offers a competitive benefits package, including not but limited to medical, dental, vision, paid time off, a 401(k) plan with employee and company contribution opportunities, life, disability, and accident insurance, and tuition reimbursement.Additional InformationGE HealthCare offers a great work environment, professional development, challenging careers, and competitive compensation. GE HealthCare is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.
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
Application Deadline: April 03, 2025 ApplyJob Profile
Legal authorization to work in the U.S. is required Must be willing to travel No Visa Sponsorship Remote U.S. based U.S. based positions only Willing to travel
Benefits/PerksAccident Insurance Career opportunities Cash bonuses Challenging careers Collaboration Collaboration and support Competitive benefits Competitive benefits package Competitive compensation Dental Flexibility Global strength and scale Great work environment Life, disability, and accident insurance Medical Medical, Dental, Vision Paid Time Off Professional development Support Total Rewards Tuition reimbursement Vision
Tasks- Collaboration
- Compliance
- Design
- Design reviews
- Development
- Documentation
- Ensure program compliance
- Guide software development plans
- Participate in audits
- Perform other duties as assigned
- Project management
- Quality assurance
- Support nonconformance evaluations
21 CFR Part 820 Agile AI Automation CAPA Clinical Clinical applications Collaboration Compliance Computer Computer Science Design Controls Design Validation Design verification Digital solutions Documentation Efficiency Engineering External audits FDA FDA CFR 21 820 Flexibility Healthcare IEC 62304 Implementation Integrity Internal Audits ISO ISO 13485 ISO 14971 IT Lean Management Manufacturing Medical device Medical device QMS Medical Devices Monitoring Nonconformance evaluations Organization Process Process controls Project Management Quality Quality Assurance Quality Management Quality Management System Radiology Regulatory Affairs Reimbursement Risk Management Software Software Development Teams Technical Technical Aptitude Technical Documentation Technology Ultrasound Validation
Experience3 years
EducationAS Bachelor Bachelor's degree in Computer Science Bachelor's degree in engineering Business Computer Science Degree Engineering Equivalent Healthcare IT Project Management Radiology Regulatory affairs Science Software Development Technology
Certifications TimezonesAmerica/Anchorage America/Chicago America/Denver America/Los_Angeles America/New_York Pacific/Honolulu UTC-10 UTC-5 UTC-6 UTC-7 UTC-8 UTC-9