GE HealthCare

Medical Director

• Define and drive the clinical strategy for the assigned care area (oncology)
• Lead the development of Target Product Profiles (TPPs), Integrated Evidence Generation Plans (IEGPs), and clinical development plans
• Represent the therapeutic area in governance forums and regulatory interactions
• Engage with KOLs and external experts to shape development strategy
• Oversee cross-functional alignment across Regulatory, Medical Affairs, Commercial, and Clinical Operations
• Mentor and guide clinical scientists and medical monitors working within the care area
• Provide medical oversight for one or more clinical trials
• Review safety data, assess adverse events, and support dose modifications or protocol amendments
• Respond to investigator queries and support site engagement
• Participate in Data Safety Monitoring Boards (DSMBs) and internal safety reviews
• Contribute to clinical study reports (CSRs), regulatory submissions, and medical writing
• Collaborate with Clinical Operations and Pharmacovigilance teams

Senior Medical Director

Program Manager

• Lead day‑to‑day execution of complex AI‑driven digital programs, coordinating across global, cross‑functional teams including software engineering, ML engineering, regulatory, clinical, and cybersecurity.
• Drive AI Development Lifecycle (AI‑DLC) execution from concept ideation, data strategy, model development, validation, deployment, post‑market monitoring, and lifecycle optimization.
• Lead tollgate execution for NPI, requisition, and sustaining programs, ensuring alignment with customer CTQs, regulatory expectations, and AI/ML governance requirements.
• Oversee delivery of AI‑enabled initiatives, including proof‑of‑concepts, algorithm development, platform releases, cloud and edge deployments, clinical/pilot trials, and install base enhancements.
• Champion the use of Generative AI tools across the development lifecycle (ideation, requirements generation, design, coding, testing, documentation, risk analysis, and commercialization readiness).
• Collaborate with business segments, enterprise partners, regulatory and quality teams, and third‑party vendors to deliver safe, effective, explainable, and compliant AI solutions.
• Define, apply, and continuously improve AI‑inclusive execution methodologies, agile/DevOps practices, and program management standards used across digital programs.
• Identify and proactively manage AI‑specific risks, including data quality, model bias, transparency, cybersecurity, clinical validation, scalability, and regulatory readiness.
• Communicate program progress, AI maturity, risks, and critical decisions with clarity and consistency to senior leadership and key stakeholders.
• Apply strong technical and product judgment to resolve moderately complex AI, software, platform, and operational challenges.
• Use data‑driven insights, analytics, and cross‑functional inputs to drive decision‑making and recommend scalable, customer‑focused AI solutions.

Senior Program Manager

Director

• The Intelligence Director for the Resilience Center of Excellence plays a critical role in enabling an anticipatory, data-driven, and action-oriented risk and resilience posture across business operations.
• This role is responsible for developing, integrating, and operationalizing real-time and forward-looking intelligence that informs both strategic, long-term risk mitigation and short-term risk monitoring, escalation, and response.
• Build, manage, and continually refine the enterprise’s intelligence framework spanning geopolitical risk, supply chain risk, regulatory changes, climate and physical threats, technology disruptions, and emerging operational hazards.
• Conduct ongoing analysis of global and regional risk signals; integrating internal data and external intelligence to generate decision-relevant insights tailored for Segments and Functions.
• Produce and deliver actionable risk assessments with explicit implications for business continuity, supply chain resiliency, customer commitments, and operational execution.
• Lead daily monitoring of acute risk indicators (weather events, geopolitical escalations, industrial action, transportation/logistics disruptions, supplier instability).
• Generate timely intelligence during crisis or incident response efforts, ensuring leadership has a clear understanding of developments of a situation/incident and potential impact.
• Design, deploy and manage a hybrid intelligence ecosystem, leveraging traditional research driven intelligence methods alongside external risk intelligence platforms to support global risk monitoring and analysis.
• Directly manage and develop intelligence analysts and/or contractors, including goal setting, performance management, coaching, and capability development.

Resilience Intelligence Director

Systems Engineer

• Provide first-class service and support to GE Healthcare Solution for Enterprise Imaging (SEI) customers through a team of technical specialists for Radiology RIS, PACS and Cardiology IT solutions
• Act as a Senior IT System Engineer interfacing with the customers, respond to reported incident issues, attend regular service support visits
• Support a remote team of installation & upgrade on site, perform software O/S patching or Safety updates when needed
• Manage customer expectations, and ensure clear communication between the customer and GEHC
• Perform structured fault analysis across complex IT environments (servers, networks, applications)
• Analyze system, performance, and stability issues and implement sustainable solutions, including updates and upgrades
• Provide independent on‑site and remote troubleshooting, support Incident, Problem, and Change Management processes, and ensure high system availability and technical quality
• Manage service activities end‑to‑end, ensure SLA compliance, response times, and customer satisfaction
• Maintain accurate system documentation, configurations, tickets, and service reports while adhering to quality, safety, and compliance requirements
• Collaborate closely with internal teams (Service, Engineering, Support, Sales) and external partners, and contribute to IT projects such as migrations, upgrades, and new system architectures

Senior IT System Engineer

Field Engineer

• Maintain all models specific to a modality in the assigned area.
• Perform total system level trouble-shooting on complex multi-symptom problems.
• Communicate clearly with end-users and department managers on equipment status; maintain customer satisfaction.
• Assist in Account Sales visits, help train others where necessary, and identify Sales opportunities and communicate them to account team.
• Assist in the growth and direction of business in geographic area.
• Responsible for Warranty and PMS contract cost control.
• Responsibly complete all administration tasks on time (e.g., ensure timely completion of FMI’s and PMS inspections documentation for assigned accounts).
• Play a leading role in complex and multifunctional rooms.
• Share best practices.
• Maintain effective quality systems and programs compliant with ISO 9001 standard, according to the GE Service Quality Policy Statement.

Field Service Engineer, RX/CT/RM

• Define and drive the clinical strategy for the assigned care area (molecular imaging)
• Lead the development of Target Product Profiles (TPPs)
• Represent the therapeutic area in governance forums and regulatory interactions
• Engage with KOLs and external experts to shape development strategy
• Oversee cross-functional alignment across Regulatory, Medical Affairs, Commercial, and Clinical Operations
• Mentor and guide clinical scientists and medical monitors working within the care area
• Provide medical oversight for one or more clinical trials
• Review safety data, assess adverse events, and support dose modifications or protocol amendments
• Respond to investigator queries and support site engagement
• Participate in Data Safety Monitoring Boards (DSMBs) and internal safety reviews
• Contribute to clinical study reports (CSRs), regulatory submissions, and medical writing
• Collaborate with Clinical Operations and Pharmacovigilance teams

Manager

• 代表公司利益与美国政府以及其他国家/地区政府和机构打交道的非律师人员
• 可以协助制定政府合同、国内产品偏好、礼品和酬金规定、前政府雇员限制条件
• 参与包括政策制定在内的长期工作
• 充当最佳实践/质量资源
• 了解自己领域的最新职能发展

Senior Government Affairs Manager

• Mantener en especificaciones todos los equipos de las distintas modalidades asignadas.
• Resolución de fallas multifactoriales en sistemas de alta complejidad.
• Relacionamiento diario con Doctores, Medicos y Técnicos en lo que respecta a atención de equipos de Imagenologia.
• Asistir al área de ventas en visitas técnicas.
• Control de costos en las garantías y contratos de servicios.

Field Service Engineer

Sales

• Deliver on quarterly & annual orders and revenue sales targets; maximize profit margin on equipment sales
• Cultivate and maintain strong relationships with healthcare stakeholders within hospital, physician practice and imaging center account service lines to identify qualified leads, grow market share, increase revenue, and reduce customer attrition
• Assist with leading cross-functional commercial teams to orchestrate deals and long-term plans that align with a mutually beneficial strategy that contributes to increased market share, revenue, and profitability
• Leverage diagnostic imaging and MR product knowledge to drive funnel growth for the region
• Demonstrate expertise in customers’ installed base and develop sales proposals that map with their annual budget process
• Lead and collaborate within the account community team to support co-developed negotiation strategies
• Reduce cycle time by leveraging Salesforce.com (CRM tool) to track customer and account activity, map visibility, drive market share, and prioritize sales funnel

MRI Regional Sales Modality Leader

Operations

• Provide strategic direction and oversight for global pharmacovigilance and drug safety operations across all regions
• Ensure compliant PV system is in place for the collection, evaluation, and submission of individual case safety reports
• Collaborate closely with PV QA team to produce clear SOPs, CAPA, quality documentation and standards for Global Pharmacovigilance
• Collaborate closely with the EU/UK QPPV to ensure PV Operations processes meet requirements
• Ensure vendor oversight for global PV including case management activities
• Own PV operational budgets, purchase orders, statements of work, and invoice oversight
• Drive process optimization, standardization, and digital innovation across PV operations
• Embrace LEAN methodologies and monitor operational metrics
• Lead change and continuous improvement activities in global PV Operations

Director, Global PV Operations

Software Engineer

• Responds to service calls to evaluate, diagnose, and perform repair and planned maintenance (PM) on customers' basic biomedical equipment.
• Drives customer satisfaction through service excellence.
• Under supervision, evaluate basic customer biomedical equipment issues, implement appropriate repairs, and as assigned, perform PM and safety/environmental inspections.
• May assist more experienced technicians on basic and more complex repairs/resolution.
• Effectively communicate and partner with teammates and colleagues.
• Follow appropriate GE policies, procedures, hospital protocol, and completes necessary documentation.
• Maintain daily communications with customers as directed, to ensure resolution and proper follow-up, leading to strong customer relations and ongoing customer satisfaction.
• As instructed, implement GE/customer facility contract and supports business goals/objectives.
• Work as a member of local team to provide efficient service delivery to all accounts within the assigned area.
• When trained, able to share on-call responsibility.
• Document all repair actions and submit reports/summaries according to schedule.
• Ensure proper care of spares, tools, and test equipment, and ensure calibration.
• Enhance and maintain technical knowledge of current standards, codes, and procedures regarding safe and effective use of medical equipment through formal instruction.
• Understand and utilize sources of help (i.e., manuals, tech support, Facetime app, online resources) to answer questions when performing PM.

Biomedical Engineering Technician, Level 1

• Define, lead and drive the regional regulatory strategy across the entire product lifecycle, including development, registration and post‑authorization activities, in compliance with EMA, CMDh, national competent authorities and Health Canada requirements.
• Apply strategic regulatory thinking to anticipate regulatory risks and opportunities, enabling informed decision‑making for products in development as well as legacy products seeking new indications or markets.
• Provide early, proactive regulatory input to development programs in support of the global Regulatory Affairs (RA) team, and influence clinical, CMC and data‑generation strategies to facilitate successful approvals.
• Ensure close collaboration between the team and global RA for effective product lifecycle management, including variations, renewals, post‑authorization commitments and regulatory actions related to safety, while ensuring compliance.
• Work closely with global RA to integrate local regulatory requirements and strategy into the product’s global regulatory strategy and requirements.
• Serve as the senior regulatory interface with the EMA and EU national authorities, leading scientific advice requests, regulatory meetings and complex negotiations.
• Lead, develop and coach the Regulatory Affairs team, ensuring clear accountability, well‑defined roles and skills development.
• Contribute to overall regulatory governance, standardization and continuous improvement initiatives within PDx.
• Support structured knowledge transfer, handover and risk‑management activities to ensure regulatory continuity.
• Drive initiatives to improve regulatory efficiency and proactively manage non‑compliance risks.
• Participate in due diligence activities related to product development, acquisitions and inbound licensing opportunities; assess regulatory risks and requirements.
• Contribute to the Regulatory Affairs function’s budget planning.

Senior Director, EU Direct, A&Z, Canada

• OMLP is a 2-year program consisting of 3 eight-month rotations that allow members to build leadership and functional skills through challenging rotational assignments and world-class training.
• Typical rotations include one or more of the following: • Manufacturing Shop Operations Supervisor • Sourcing/Materials Management (procurement, material flow) • Technical – (lean, manufacturing engineer / process engineer) • Environment, Health & Safety (site operations support, EHS media support)

Operations Management Leadership Program

Analyst

• Own core treasury functions: cash management, intercompany funding, trade finance, FX risk management, bank solutions and relationship.
• Partner with business units to deliver tailored treasury solutions that support growth and mitigate risk.
• Optimize cash management structures and drive yield-enhancing strategies across the region.
• Lead trade finance issuances and activities, including managing bank guarantees, SBLCs, surety bonds, bank reconciliation, fee payment and credit lines.
• Collaborate with global and regional stakeholders to streamline processes and enhance treasury activities.
• Advise on treasury aspects of commercial deals and regulatory environments.
• Drive strategic projects and process improvements that deliver measurable impact.
• Report key metrics and insights to senior leadership, keeping them informed and empowered.
• Support broader regional treasury activities as needed.
• Provide backup coverage for other regional treasury teams for planned/unplanned absences, holiday coverage or outages.

Regional Treasury Lead Analyst

• Lead and oversee the regulatory strategy in the region across the product lifecycle.
• Apply strategic regulatory thinking to anticipate regulatory risks and opportunities.
• Provide early, proactive regulatory input to development programs supporting the RA Global team.
• Ensure compliance and collaborate with the RA global team for effective lifecycle management.
• Serve as the senior regulatory interface with the commercial team in the region.
• Lead, develop, and mentor the Regulatory Affairs team, ensuring clear accountability.

Senior Medical Director

Senior Program Manager

Resilience Intelligence Director

Senior IT System Engineer

Field Service Engineer, RX/CT/RM

Senior Medical Director

Senior Government Affairs Manager

Field Service Engineer

MRI Regional Sales Modality Leader

Director, Global PV Operations

Biomedical Engineering Technician, Level 1

Senior Director, EU Direct, A&Z, Canada

Operations Management Leadership Program

Regional Treasury Lead Analyst

Senior Director, EU Indirect, MEACAT