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GE Healthcare

Imaging, monitoring, and healthcare IT solutions

Quality Assurance Lead Engineer

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeWaukesha, WI, USANo salary listed

About the Job

Requirements

  • A bachelor's degree in an engineering or technical discipline, or a high school diploma with a minimum of seven years of experience in manufacturing, engineering, or quality assurance.
  • A minimum of three years of experience working in a regulated industry.
  • Demonstrated understanding of, or aptitude to understand, medical device Quality Management System requirements and regulatory requirements, including FDA CFR 21 820 and ISO 13485.
  • Willingness to work a hybrid schedule with three days per week on-site at the GE HealthCare office in Waukesha, Wisconsin.
  • Flexibility in work hours and willingness to partner with and accommodate global teams and schedules.

Responsibilities

  • Create a quality culture by driving compliance activities around a specific product, site, or region, including responsibility for the business's total Quality Management System and Quality metrics.
  • Ensure quality and regulatory compliance while driving process effectiveness and efficiency.
  • Represent GE Healthcare to external agencies and champion the evolution of the quality culture, including executing and driving quality objectives, metrics, reporting, and operating mechanisms.
  • Develop in-depth knowledge of a discipline.
  • Use prior experience and acquired expertise to execute functional policy and strategy.
  • Communicate with direct colleagues and the business about design and coordination services rendered.
  • Provide informal guidance to new team members.
  • Explain complex information to others in straightforward situations.
  • Impact projects, processes, and procedures in the role's field.
  • Operate with some autonomy, focused on executing activities and providing advice within an enabling discipline covered by standard functional practices and procedures.
  • Exercise professional judgment while performing activities that may require guidance from more senior staff.
  • Use technical expertise and judgment to solve problems.
  • Leverage technical skills and analytic thinking to solve problems.
  • Use multiple internal sources outside the team as needed to arrive at decisions.

Desired Qualifications

  • Knowledge of Quality Management System tools, continuous improvement methodologies, site-level products, and related processes.
  • Understanding of product development lifecycles, design change and document change control, process verification and validation methodologies, manufacturing and production process control methodologies, and servicing in a medical device environment.
  • Ability to communicate effectively at all organizational levels about design controls, design verification and validation activities, production and process controls, Corrective and Preventive Action, complaints and risk management, and product quality improvement using tools such as Six Sigma and DFR.
  • Collaboration, negotiation, and conflict resolution skills.
  • Ability to lead, acknowledge, develop, communicate, and implement a strategy to ensure compliance.
  • Oral communication, report writing, business correspondence, and procedure-writing skills.
  • Ability to lead, acknowledge, develop, communicate, and implement a strategy under crisis situations to ensure compliance.
  • Ability to drive change as a change agent.
  • Analytical, problem-solving, and root-cause analysis skills.
  • Ability to multitask and handle tasks with competing priorities effectively.
  • Understanding of customer needs, marketplace dynamics, industry trends, and the competitive landscape in the industry or function, and consideration of the external impact of business activities and decisions.
  • Ability to simplify strategy into specific actions with clear accountability, make decisions with speed and accuracy based on the best available information, and communicate priorities clearly and concisely.

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

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