Job Overview
Location
Remote
Job Type
Full-time
Category
Human Resources
Date Posted
July 1, 2026
Full Job Description
đź“‹ Description
- • The Global Quality Assurance Auditor, Pharmacovigilance role at GE HealthCare Technologies Inc. is responsible for providing QA auditing for the Pharmaceutical Diagnostics (PDx) business, with a focus on GMP manufacturing sites and Pharmacovigilance (PV) functions to ensure global compliance and drive continuous improvement.
- • Day-to-day responsibilities include planning, preparing, and executing internal and external audits; ensuring timely remediation of audit findings; supporting regulatory inspections as a QA subject matter expert; conducting trend analysis of audit and quality data; managing vendor qualification and surveillance activities; participating in QMS improvements; guiding CAPA processes; and staying current with regulatory guidelines from MHRA, FDA, EMEA, and other bodies to inform procedural updates.
- • The role operates within GE HealthCare’s Pharmaceutical Diagnostics business, supporting global compliance efforts across manufacturing and pharmacovigilance functions, with a focus on proactive risk identification and process improvement through data-driven insights and regulatory awareness.
- • The auditor will develop expertise in global pharmaceutical regulations, audit management, CAPA systems, and quality trend analysis, while building influence in cross-functional collaboration and driving compliance culture across international sites.
🎯 Requirements
- • Bachelor’s degree from an accredited university or college (or high school diploma/GED with at least 8 years of pharmaceutical industry experience)
- • 6+ years of experience in the pharmaceutical industry
- • Previous auditing experience required
- • Experience interfacing with global regulatory agencies
- • Ability to comprehend and communicate key regulatory requirements and expectations
- • Knowledge of GPvP, cGMP, and GDP
🏖️ Benefits
- • Remote work flexibility
- • Opportunity to work with global regulatory agencies and influence compliance strategy
- • Involvement in quality management system improvements and CAPA process leadership
- • Exposure to trend analysis and data-driven quality initiatives across pharmaceutical diagnostics
- • Professional growth in auditing, regulatory compliance, and pharmaceutical quality systems
Skills & Technologies
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About GE HealthCare Technologies Inc.
GE HealthCare Technologies Inc. designs, manufactures and services medical imaging, diagnostics, monitoring and life-care equipment for hospitals, clinics and research institutions worldwide. The company’s portfolio includes MRI, CT, ultrasound, X-ray and molecular imaging systems, contrast agents, pharmaceutical diagnostics, ventilators and anaesthesia machines, enterprise digital solutions, and after-sales support, training and financing services. Headquartered in Chicago, Illinois, it operates manufacturing, R&D, sales and service facilities across North America, Europe and Asia.
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