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Job Description Summary GE Healthcare Fabrikk Oslo på Storo produserer sterile og aseptiske kontrastmidler. Kvalitetssikringsområdet innen Fabrikk Oslo har hovedansvar for kvalitetssikring av systemer, prosesser, lokaler og prosjekter, samt frigivelse av produkter til salg. Området består av to avdelinger: QA systemer og Dokumentasjon og batch release. For å styrke kvalitetssikringsavdelingens kompetanse og kapasitet hos QA systemer søker vi etter en person med bachelorutdannelse i realfag med interesse for kvalitetssikring. Stillingen er midlertidig, på ett år. GE HealthCare's Oslo factory in Storo produces sterile and aseptic contrast media. The Quality Assurance organization within the Oslo factory has overall responsibility for quality assurance of systems, processes, facilities, and projects, as well as for the release of products for sale. The organization consists of two departments: QA Systems and Documentation & Batch Release. To strengthen the competence and capacity of the Quality Assurance department within QA Systems, we are seeking a candidate with a bachelor's degree in a scientific discipline and an interest in quality assurance. This is a temporary position for a period of one year. Job Description Jobbsammendrag Vi søker en engasjert og kvalitetsbevisst Kvalitetssikringsspesialist til GE HealthCare AS. Rollen vil være sentral i å sikre kvalitet og regulatorisk etterlevelse innen steril og aseptisk legemiddelproduksjon. Du vil ha et særlig ansvar for kvalitetssikring av SAP-relaterte prosesser og godkjenning av artwork og emballasjemateriell, samt bidra til kontinuerlig forbedring gjennom en LEAN-basert tilnærming. Stillingen gir en unik mulighet til å påvirke kvalitet, effektivitet og pasientsikkerhet i et internasjonalt og høyt regulert miljø. Arbeidsoppgaver Sikre etterlevelse av GMP-krav og kvalitetsstandarder innen steril og aseptisk legemiddelproduksjon. Utføre kvalitetsrelaterte vurderinger og godkjenninger i SAP, herunder materialmasterdata, spesifikasjoner, produktstrukturer og endringsprosesser. Godkjenne artwork, etiketter, emballasjemateriell og tilhørende endringer for å sikre samsvar med regulatoriske krav og produktspesifikasjoner. Gi kvalitetssikringstøtte til produksjonsområder, laboratorier og støttefunksjoner. Bidra til kontinuerlig forbedring gjennom LEAN-prinsipper og strukturerte problemløsningsmetoder. Analysere kvalitetsdata og trender for å identifisere forbedringsmuligheter og styrke kvalitetssystemet. Utarbeide, revidere og godkjenne prosedyrer, arbeidsinstrukser og annen GMP-dokumentasjon. Delta i interne og eksterne revisjoner samt myndighetsinspeksjoner og sikre effektiv oppfølging av observasjoner. Bidra til opplæring og veiledning innen GMP, aseptisk adferd, dataintegritet og kvalitetsprosesser. Delta i håndtering av avvik, kvalitetsundersøkelser, CAPA og endringskontroll etter behov. Kvalifikasjoner Bachelor- eller mastergrad innen farmasi, kjemi, bioteknologi, ingeniørfag eller tilsvarende relevant utdanning. Erfaring fra farmasøytisk industri, fortrinnsvis innen steril eller aseptisk produksjon. God kunnskap om GMP-regelverk, inkludert EU GMP og Annex 1. Erfaring med SAP og kvalitetsrelaterte prosesser knyttet til masterdata, materialhåndtering eller produktvedlikehold. Erfaring med godkjenning av artwork, etiketter eller emballasjemateriell. Gode analytiske evner og en strukturert tilnærming til problemløsning. Gode samarbeidsevner og evne til å kommunisere på tvers av fagområder. Flytende norsk og engelsk, både muntlig og skriftlig. Det er en fordel om du har erfaring med Avvikshåndtering, CAPA og endringskontroll. LEAN, Operational Excellence eller kontinuerlig forbedringsarbeid. Risikostyring og revisjoner i regulerte miljøer. Strukturerte problemløsningsmetoder English job description Job Summary We are seeking a motivated and quality-focused Quality Assurance Specialist to join GE HealthCare AS. This role will be instrumental in ensuring quality and regulatory compliance within sterile and aseptic pharmaceutical manufacturing. The role will have a particular focus on quality assurance of SAP-related processes and the approval of artwork and packaging materials, while also driving continuous improvement through a LEAN-based approach. This position offers an opportunity to influence quality, operational efficiency, and patient safety in an international and highly regulated environment. Key Responsibilities Ensure compliance with GMP requirements and quality standards within sterile and aseptic pharmaceutical manufacturing. Perform quality-related assessments and approvals in SAP, including material master data, specifications, product structures, and change processes. Approve artwork, labels, packaging materials, and associated changes to ensure compliance with regulatory requirements and product specifications. Provide quality assurance support to manufacturing operations, laboratories, and support functions. Contribute to continuous improvement through LEAN principles and structured problem-solving methodologies. Analyze quality data and trends to identify improvement opportunities and strengthen the quality management system. Prepare, revise, and approve procedures, work instructions, and other GMP documentation. Participate in internal and external audits, as well as regulatory inspections, and ensure effective follow-up of observations. Support training and coaching in GMP, aseptic behavior, data integrity, and quality processes. Participate in the management of deviations, quality investigations, CAPA activities, and change controls as required. Qualifications Bachelor's or Master's degree in Pharmacy, Chemistry, Biotechnology, Engineering, or a related scientific discipline. Experience from the pharmaceutical industry, preferably within sterile or aseptic manufacturing. Strong knowledge of GMP regulations, including EU GMP and Annex 1. Experience with SAP and quality-related processes involving master data, material management, or product maintenance. Experience with approval of artwork, labels, or packaging materials. Strong analytical skills and a structured approach to problem solving. Excellent collaboration and communication skills, with the ability to work effectively across multiple functions. Fluent in Norwegian and English, both written and spoken. Preferred Qualifications Experience with the following is considered an advantage: Deviation management, CAPA, and change control. LEAN, Operational Excellence, or continuous improvement initiatives. Risk management and auditing in regulated environments. Structured problem-solving methodologies. #LI-PW1 Additional Information Relocation Assistance Provided: No

Job Description Summary We are looking for an experienced Software Engineer (Qt/QML) to join the Maternal & Fetal Care (MFC) Systems & Software Engineering team. In this role, you will be a core member of the product software team responsible for designing, developing, integrating, testing, and maintaining high-quality software for MFC products. You will contribute to software architecture, feature development, defect resolution, performance improvement, and sustaining activities in a regulated medical device environment. The ideal candidate is a strong team player with excellent communication skills, hands-on technical depth, and the ability to deliver results in a fast-paced Agile environment. GE Healthcare is a leading global medical technology and digital solutions innovator. Our mission is to improve lives in the moments that matter. 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 ­­Roles and Responsibilities: In this role, you will: Design, develop, integrate, and maintain software features, platform components, subsystems, and services for Infant Care products. Develop high-quality C++, Qt, and QML software on embedded Linux platforms, ensuring reliability, maintainability, scalability, and performance. Apply SDLC practices and methodologies such as Agile, Lean, CI/CD, software and product security, documentation, refactoring, and testing techniques. Write clean, efficient, testable code that meets coding standards and delivers the expected functionality within committed timelines. Work with product, technical, program, and system leadership to understand product requirements, user needs, product vision, and multi-generation technology plans. Translate requirements and product vision into well-defined user stories, software tasks, design inputs, and implementation plans. Participate in software design reviews, code reviews, interface definition, impact analysis, and technical decision-making. Analyze defects, perform root cause investigation, debug complex software issues, and implement corrective actions. Collaborate with verification, systems, hardware, program, and product teams to ensure complete and high-quality feature delivery. Support unit testing, integration testing, automation, static analysis, and other engineering practices that improve software quality and predictability. Understand the complete product, its modules, interfaces, and dependencies while developing expertise in the assigned component or subsystem. Identify opportunities to improve development efficiency, reduce duplication, increase reuse, and strengthen software development processes. Ensure compliance with applicable quality, regulatory, security, documentation, and process expectations for medical device software. Qualifications/Requirements: Bachelor’s degree in STEM discipline such as Computer Science, Electronics, Electrical Engineering, Biomedical Engineering, or a related field. Minimum of 3 years of professional software development experience in a production software environment. Strong hands-on experience in C++, Qt, QML, and object-oriented analysis and design on embedded Linux platforms. Experience working in Agile software development teams with exposure to SDLC, CI/CD, version control, code reviews, and defect management practices. Strong debugging and problem-solving skills, including experience working with existing and complex codebases. Ability to work independently with minimal supervision while collaborating effectively with cross-functional and global teams. Desired Characteristics: Experience in medical device software development or other regulated product development environments. Understanding of healthcare product development, quality management systems, design controls, traceability, verification, and validation practices. Proficiency in leveraging approved AI-assisted software development tools to enhance coding efficiency, test automation, code quality, debugging effectiveness, and overall engineering productivity while adhering to security, compliance, and quality standards. Experience with unit testing, integration testing, test automation, static analysis, performance profiling, and software quality improvement practices. Exposure to tools such as Git, GitLab, Jenkins, Jira, Rally, Coverity, SonarQube, or similar engineering toolchains. Strong analytical thinking, ownership mindset, communication skills, and ability to work with global cross-functional teams across time zones. Proven ability to ramp up quickly on complex and unfamiliar codebases and learn new languages, frameworks, tools, or product domains as needed. Note This Job Description is intended to provide a high level guide to the role. However, it is not intended to amend or otherwise restrict/expand the duties required from each individual employee as set out in their respective employment contract and/or as otherwise agreed between an employee and their manager. Additional Information Relocation Assistance Provided: Yes

Job Description Summary The Digital Adoption Sales Specialist plays a critical role in accelerating the adoption and commercial success of digital solutions in Radiation Oncology. This role is responsible for promoting, demonstrating, and managing trials of digital tools and platforms, while driving customer success, satisfaction, and long-term engagement. Working closely with Sales Account Managers and Product Specialist teams, the Digital Adoption Specialist ensures seamless integration of digital solutions into clinical workflows, expands share of wallet within existing accounts, and supports margin growth through value-based selling. Job Description Key Responsibilities • Digital Solution Promotion & Trials Lead product demonstrations and manage digital solution trials to support adoption of Radiation Oncology software and platforms . Define and execute the trial strategy to maximize impact and conversion. Collaborate with sales and product teams to ensure trials are integrated into broader commercial strategies and lead to long-term adoption. Develop and execute customer engagement programs such as symposiums, congresses, hands-on sessions, and webinars. • Customer Success & Engagement Drive customer success plans and act as the primary point of contact for Radiation Oncology solution users , ensuring high satisfaction, effective usage, and continuous value realization. • Commercial Enablement Collaborate closely with Sales Account Managers and Product Specialists to increase the attachment rate of digital solutions across all Radiation Oncology opportunities . Demonstrate the combined clinical and operational value of integrating digital platforms with imaging and oncology systems to drive synergy across hardware, software, and service sales. Identify upsell and cross-sell opportunities within existing accounts, contributing to revenue growth, margin expansion, and increased share of wallet. Support the sales team with tailored messaging, value propositions, and tools that highlight the strategic benefits of digital adoption in Radiation Oncology workflows . • Training & Education Alignment Ensure customer satisfaction by identifying specific training needs and aligning them with the Clinical Education team. Act as a liaison between the customer and internal training resources to ensure that educational programs are tailored to the clinical and operational requirements of each site. Support the planning and coordination of training delivery, ensuring a smooth onboarding experience and optimal use of digital solutions. • Feedback & Product Improvement Gather user feedback and usage data to inform product development and enhancements, acting as the voice of the customer within the organization. • Performance Monitoring Track adoption metrics, usage patterns, and customer satisfaction KPIs to drive continuous improvement and demonstrate ROI to stakeholders. • Strategic Account Development Support strategic account planning by identifying digital growth opportunities and aligning with broader commercial objectives. • Sales Accountability Responsible for achieving financial targets related to MIM Software and Radiation Oncology digital solution sales , both as standalone deals and as part of combined offerings. Work in partnership with Sales Account Managers and Product Sales teams to drive revenue, margin, and share of wallet expansion. • Collaboration with Digital Implementation Teams Work closely with the Imaging Digital Solutions team responsible for IT implementation. Define the best structure and offering during the sales process to align with customer needs, ensuring a smooth and proper installation of digital solutions. Required Qualifications Bachelor’s degree in Healthcare, Biomedical Engineering, Health IT, or a related field. 3+ years of experience in healthcare technology, digital health, or clinical applications, preferably within Radiation Oncology, Oncology Informatics, or healthcare software . Strong understanding of Radiation Oncology workflows and digital health ecosystems. Desired Characteristics Excellent communication and interpersonal skills, with the ability to engage both clinical and technical stakeholders. Demonstrated success in customer-facing roles, including training coordination, onboarding, or customer success. Experience with digital platforms, SaaS models, or enterprise healthcare software. Strong analytical mindset with the ability to interpret usage data and customer feedback. Collaborative team player with a proactive, solution-oriented approach. About Us GE HealthCare is a leading global medical technology and digital solutions innovator with over 100 years of healthcare industry experience and approximately 50,000 employees worldwide. We enable clinicians to make faster, more informed decisions through intelligent devices, data analytics, applications, and services, supported by our Edison intelligence platform. We operate at the center of an ecosystem working toward precision health by digitizing healthcare, helping drive productivity, and improving outcomes for patients, providers, health systems, and researchers around the world. Our total rewards are designed to unlock your ambition by providing the flexibility and support needed to turn your ideas into world-changing realities. Our salary and benefits are everything you would expect from an organization with global strength and scale, and you will be surrounded by career opportunities in a culture that fosters care, collaboration, and support. GE HealthCare is an Equal Opportunity Employer where inclusion matters. 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 – Creating a world where healthcare has no limits # LI-SV1 Additional Information Relocation Assistance Provided: No

Job Description Summary As a full stack developer in Imaging Platform team, you’ll be responsible for designing, building, delivering and maintaining next generation platform solutions for GE Healthcare Products. This platform includes Kubernetes as microservice orchestrator with different platform services for messaging, database, caching, DICOM, Camera, etc. Requires 3-6 years of hands-on development experience in microservice development using GO or Java, containerization using Kubernetes / Docker on Linux Env, deployment and packaging using helm, Python and Ansible. Responsible for end-to-end software delivery including activities such as feature grooming, requirement analysis, documentation/procedures, technology assessment, implementation, code reviews and formal release activities. Job Description Responsibilities: Collaborate with software developers and imaging teams to implement solutions that are aligned with and extend shared platforms and solutions. Apply Agile principles of Software Development Life Cycle and methodologies, Software and Product Security, Scalability, Documentation Practices, refactoring and Testing Techniques. Writes codes that meets standards and delivers desired functionality using the technology selected for the project. Build common microservices for Healthcare Imaging platform and healthcare solution using microservices architecture. Actively participate in grooming , PI planning, sprint reviews and demos. Perform Technical feasibility assessment and share outcomes that help conclude technology decisions. Understand performance parameters, assess application performance and address security issues. Ensure unit test automation using BDD and consistent code quality by adhering to SONAR quality gates. Activity manage formal verification and release activities. Coordinate with internal team members and other imaging teams for platform integration and defect fixes. Education Qualification Bachelor’s Degree in Computer Science or in “STEM” Majors (Science, Technology, Engineering and Math) . Master’s Degree in Computer Science/Maths or related field. A minimum of 3 to 6 years of professional experience (include technical skill) Primary Skills Minimum of 3 + years of software development experience. Python, Inferencing Engine (Onyx, Open Vino, Tensor Flow and Triton) and AI Model deployment Experience in containerization technologies like Kubernetes/Docker. HELM Charts, YAML, Ansible, Python, Shell scripting. Rest based microservice development using GO/Python/Java. BDD based automated testing using Cucumber. Good communication and presentation skills Inclusion and Diversity GE Healthcare is an Equal Opportunity Employer where inclusion matters. 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. 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. #LI-Hybrid #LI-MP2 Additional Information Relocation Assistance Provided: Yes

Job Description Summary The Staff Cyber Security Engineer will serve as the Product Security Representative (PSR) for AIS Digital Ecosystems – Imaging360, a cloud-enabled enterprise healthcare platform that connects with on-premises imaging scanners and integrates with third-party products and services. This role is responsible for embedding cybersecurity, privacy, and regulatory expectations into product design, software development, cloud operations, integrations, and lifecycle management. The successful candidate will partner with Product Security Leaders, engineering, architecture, product management, cloud operations, quality, compliance, and external vendor teams to ensure Imaging360 follows the GE HealthCare Design Engineering Privacy and Security (DEPS) process. The role requires strong experience securing enterprise-scale cloud products, distributed healthcare workflows, hybrid cloud/on-premises connectivity, APIs, identity and access management, third-party integrations, vulnerability management, and secure product lifecycle practices. The Senior Cyber Security Engineer will be expected to leverage open-source technology and industry standard programming languages to enhance cyber security operations. Success in this role will require delivery of engineering, software development, and build-automation projects in an agile environment. GE Healthcare is a leading global medical technology and digital solutions innovator. Our mission is to improve lives in the moments that matter. 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 Key Responsibilities Serve as the Product Security Representative for multiple Imaging360 products and releases, representing cybersecurity and privacy requirements throughout the product lifecycle. Drive execution of the GEHC DEPS process, including security and privacy planning, threat modeling, cybersecurity risk assessment, secure design reviews, vulnerability management, lifecycle security artifacts, and phase-appropriate security deliverables from concept through development and evaluation. Own Security Design Reviews across the product lifecycle, including concept definition, architecture and design, development execution, verification / evaluation, and release readiness for Imaging360 capabilities and integrations. Partner with Product Security Leaders and product teams to interpret and apply GEHC cybersecurity standards, regulatory expectations, and quality management system requirements. Lead threat modeling and security architecture reviews for cloud-hosted enterprise applications, APIs, data flows, scanner connectivity, on-premises integrations, identity services, and third-party product integrations. Assess cybersecurity risks associated with hybrid deployments involving cloud services, customer networks, on-premises scanners, edge components, and external vendor systems. Define and influence implementation of security controls for authentication, authorization, encryption, audit logging, secrets management, network segmentation, secure communication, data protection, and system hardening. Own or support cybersecurity management plans, vulnerability triage, remediation planning, risk acceptance discussions, and closure tracking across multiple product teams. Coordinate SAST, SCA, DAST, penetration testing, infrastructure scanning, container security, cloud security reviews, and remediation activities in partnership with engineering and operations teams. Generate, maintain, and assess Software Bill of Materials (SBOM) content, including open-source, commercial, and third-party components integrated into the product. Evaluate third-party product integrations for cybersecurity, privacy, data protection, interface security, supportability, and operational risk. Collaborate with architecture, platform, DevOps, cloud operations, quality, regulatory, privacy, and program teams to ensure secure-by-design and compliant delivery. Provide cybersecurity guidance to scrum teams, review design and implementation decisions, and help teams adopt secure SDLC and DevSecOps practices. Support fielded product security activities, including vulnerability impact assessments, customer notifications, remediation planning, patch strategy, and lifecycle risk management. Champion Imaging360-level security KPI reporting, governance dashboards, and ongoing monitoring of security health indicators, including vulnerability posture, remediation progress, open risks, security test coverage, SBOM readiness, and DEPS compliance status. Prepare clear technical and leadership-level communication on security posture, risks, remediation status, and product security readiness. Education Qualification Bachelor’s degree in Computer Science, Computer Engineering, Cybersecurity, Information Security, Software Engineering, or a related STEM discipline Technical Skill Set 12+ years of experience in software engineering, product security, application security, cloud security, or cybersecurity engineering for enterprise products. Hands-on experience securing cloud-hosted enterprise applications and distributed systems, preferably in AWS, Azure, or similar cloud environments. Experience with enterprise products that integrate with on-premises systems, connected devices, customer networks, or scanner / equipment workflows. Strong understanding of secure software development lifecycle practices, threat modeling, cybersecurity risk management, vulnerability management, and security control implementation. Working knowledge of application, API, container, infrastructure, network, and cloud security concepts. Experience with security assessment tools and practices such as SAST, SCA, DAST, penetration testing, container scanning, cloud posture management, SBOM generation, and dependency vulnerability analysis. Knowledge of OWASP Top 10, secure coding principles, identity and access management, encryption, audit logging, secure communications, and privacy-by-design principles. Ability to work effectively in a regulated product development environment and maintain compliance with quality, privacy, and cybersecurity processes. Demonstrated technical leadership, stakeholder management, and communication skills across engineering, product, quality, regulatory, security, and leadership audiences. Desired Skills Experience serving as a Product Security Representative, security architect, or product security owner for multiple products or releases. Experience with healthcare software, medical device software, imaging workflows, DICOM environments, or connected clinical systems. Familiarity with GEHC DEPS or equivalent product cybersecurity lifecycle processes in regulated industries. Understanding of applicable cybersecurity and privacy frameworks such as FDA cybersecurity guidance, NIST, ISO 27001, IEC 81001-5-1, HIPAA, GDPR, SOC 2, or similar standards. Experience assessing third-party products, SaaS services, APIs, vendor integrations, and data exchange workflows for cybersecurity and privacy risk. Hands-on experience with tools such as threat modeling tools, Black Duck, Syft, Grype, SonarQube, Burp Suite, Wiz, Twistlock / Prisma Cloud, or equivalent security platforms. Experience with DevSecOps practices, CI/CD security gates, automated security testing, infrastructure-as-code security, container security, and cloud-native monitoring. Strong understanding of identity federation and access control technologies such as SAML, OAuth, OIDC, SCIM, RBAC, and least-privilege access models. Security certifications such as CISSP, CSSLP, CISM, CCSP, CEH, or equivalent credentials are a plus. Ability to influence without authority, simplify complex security topics, and drive timely risk-based decisions across global and cross-functional teams. Inclusion and Diversity GE Healthcare is an Equal Opportunity Employer where inclusion matters. Employment decisions are made without regard to race, colour, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law. We expect all employees to live and breathe our behaviours: 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 would expect from an organization with global strength and scale, and you will be surrounded by career opportunities in a culture that fosters care, collaboration and support. #LI-Hybrid #LI-MP2 Additional Information Relocation Assistance Provided: Yes