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GE Healthcare

Imaging, monitoring, and healthcare IT solutions

Quality Assurance Manager Regional Quality

Regulatory & Quality (Life Sciences)Posted on Nov 13
Full-time

About the Job

Requirements

  • A master's degree from an accredited university or college, or a bachelor's degree and two years of relevant experience, or a high school diploma/GED with at least six years of relevant experience.
  • Strong oral and written communication skills.
  • Strong interpersonal and leadership skills.
  • Demonstrated ability to analyze and resolve problems.
  • Demonstrated ability to lead programs and projects.
  • Ability to document, plan, market, and execute programs.
  • Established project management skills.
  • Legally authorized to work in the United States; employment is conditioned upon successful completion of a drug screen, as applicable.

Responsibilities

  • Develop and maintain systems, rules, and processes to ensure fulfillment of internal and external requirements and ensure projects and products can meet specified standards.
  • Lead, coach, and develop Regional Quality team members supporting the U.S. market, ensuring operational excellence, regulatory compliance, customer focus, and effective execution of Quality responsibilities.
  • Drive engagement, clarity, accountability, and cross-functional collaboration across a geographically dispersed organization.
  • Foster a Quality and compliance culture across internal operations and external distribution partners.
  • Provide Quality leadership and governance for U.S. Regional Quality activities, primarily for radiopharmaceutical products and distribution operations, and support Contrast Media as needed.
  • Oversee the regional Quality Management System and align it with the Global QMS and applicable U.S. regulatory requirements.
  • Ensure compliance with applicable FDA requirements, cGMP, GDP distribution requirements, product-specific controls, applicable state requirements, and company Quality standards.
  • Oversee Quality across the product distribution lifecycle, including receipt, storage, handling, transportation, distribution, returns, recalls, and disposition, as applicable.
  • Oversee time- and temperature-sensitive radiopharmaceutical distribution, including required product handling and distribution controls.
  • Identify, assess, communicate, and escalate Quality and compliance risks to regional and business leadership.
  • Oversee U.S. distribution of radiopharmaceutical products across internal operations, distribution locations, logistics providers, and outsourced activities.
  • Ensure distribution processes maintain product quality, integrity, traceability, security, and supply-chain compliance.
  • Oversee Quality requirements for transportation, temperature excursions, distribution deviations, product complaints, returns, recalls, and other distribution-related Quality events.
  • Partner with Supply Chain, Operations, Regulatory Affairs, Pharmacovigilance, Medical, Commercial, and other functions to manage Quality risks effectively.
  • Support qualification, monitoring, and Quality governance of third-party logistics providers, distributors, suppliers, and other external partners.
  • Support Contrast Media distribution and Quality activities according to business priorities and regional needs.
  • Establish and monitor regional Quality objectives, KPIs, trends, and performance metrics.
  • Ensure timely and effective investigation, documentation, approval, and closure of deviations, CAPAs, complaints, change controls, temperature excursions, and other Quality records.
  • Ensure corrective and preventive actions are effective and identify recurring or systemic Quality issues through trending and management review.
  • Simplify, standardize, and continuously improve Regional Quality processes.
  • Participate in global and regional Quality initiatives and share best practices across the Pharmaceutical Diagnostics organization.
  • Maintain inspection readiness for U.S. Regional Quality and distribution activities.
  • Support and participate in regulatory inspections, internal audits, supplier and distributor audits, and other Quality assessments.
  • Represent Regional Quality in interactions with regulatory authorities and other external parties, as appropriate.
  • Ensure observations, nonconformities, and audit findings are investigated and corrective actions are completed effectively and on time.
  • Serve as a senior Quality partner to U.S. Regional, Supply Chain, Operations, Regulatory, and Commercial leadership.
  • Provide independent Quality oversight and escalate significant Quality, compliance, product, or distribution risks appropriately.
  • Balance regulatory and Quality requirements with operational needs while prioritizing patient safety, product quality, and compliance.
  • Communicate Quality performance, emerging risks, inspection readiness, and significant Quality events to leadership.

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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