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GE Healthcare

Imaging, monitoring, and healthcare IT solutions

Global Regulatory Packaging Compliance Leader

Full-Time
No salary listed
Expert
Bachelor's, Master's
Bengaluru, Karnataka, India
In PersonRelocation assistance is provided.
Biology & BiotechRegulatory & Quality (Life Sciences)

About the job

Requirements
  • A bachelor's degree in Mechanical Engineering, Regulatory Affairs, Environmental Science, or a related technical discipline.
  • At least 15 years of professional experience in Regulatory Affairs, Regulatory Compliance, Product Compliance, or a related regulated-industry function.
  • Experience in Packaging Regulatory Affairs or Regulatory Compliance within the medical device, MedTech, healthcare technology, or another highly regulated manufacturing industry.
  • Experience interpreting, assessing, and implementing regulatory requirements across multiple countries or geographic regions.
  • Ability to translate complex regulatory requirements into practical business processes, technical requirements, and implementation plans.
  • Experience leading regulatory compliance initiatives and coordinating activities across global, cross-functional teams.
  • Understanding of regulatory risk assessment, compliance documentation, governance processes, and regulatory change management.
  • Ability to independently manage complex compliance programs, establish priorities, and drive implementation through cross-functional stakeholders.
  • Ability to communicate, manage stakeholders, and influence senior leadership and global teams effectively.
  • Analytical, problem-solving, and risk-based decision-making capabilities.
Responsibilities
  • Establish a global packaging regulatory compliance framework across business segments, products, and geographic markets.
  • Monitor existing and emerging global packaging regulations, including the European Union Packaging and Packaging Waste Regulation (PPWR), Extended Producer Responsibility (EPR), and applicable country-specific packaging, environmental, recycling, and waste-management requirements.
  • Conduct regulatory applicability assessments, evaluate business and operational impacts, and communicate regulatory changes, compliance risks, and implementation priorities to stakeholders and leadership.
  • Interpret regulatory requirements and translate them into technical, engineering, packaging, quality, sourcing, and business requirements.
  • Develop regulatory implementation roadmaps, compliance calendars, readiness assessments, and cross-functional action plans.
  • Lead and coordinate PPWR regulatory assessments, technical compliance activities, and implementation initiatives with relevant global teams.
  • Establish and maintain standardized regulatory compliance processes, procedures, governance mechanisms, and documentation requirements.
  • Coordinate the preparation and maintenance of regulatory declarations, technical documentation, compliance assessments, change notifications, and supporting evidence.
  • Develop and maintain a global packaging regulatory risk register, identify compliance gaps, and coordinate risk mitigation and corrective action plans.
  • Establish regulatory compliance key performance indicators, dashboards, and monitoring mechanisms to track regulatory readiness, implementation progress, and compliance risks.
  • Coordinate EPR compliance activities, including country-specific registration, reporting, documentation, and clarification of functional ownership and accountability.
  • Partner with Regulatory Affairs, Product Compliance, Engineering, Packaging Centers of Excellence, Quality, Sourcing, Manufacturing, Sustainability, Environmental Health and Safety, Logistics, and suppliers to advance global regulatory compliance practices.
  • Develop and deliver regulatory training, compliance communications, and awareness programs.
  • Provide global leadership with updates and recommendations on regulatory developments, business risks, compliance status, and implementation progress.
  • Improve and standardize packaging regulatory compliance practices while supporting uninterrupted business operations and global market access.
Desired Qualifications
  • A master's degree in Packaging Engineering, Regulatory Affairs, Environmental Engineering, or a related discipline.
  • Knowledge of global packaging regulations, including EU PPWR, Extended Producer Responsibility (EPR), packaging waste management, recycling requirements, and environmental compliance obligations.
  • Experience in packaging regulatory compliance, packaging engineering, packaging materials, or product labeling requirements.
  • Familiarity with applicable ISO packaging and labeling standards.
  • Experience developing regulatory compliance frameworks, governance processes, implementation roadmaps, risk registers, key performance indicators, and compliance dashboards.
  • Understanding of packaging sustainability regulations, carbon footprint reduction initiatives, hazardous material restrictions, and circular economy requirements.
  • Experience supporting regulatory change notifications, compliance assessments, technical documentation, and regulatory reporting.
  • Ability to anticipate emerging regulatory risks, provide practical recommendations, and influence decisions across a global organization.
  • Regulatory judgment, cross-functional collaboration, documentation rigor, and a continuous improvement mindset.

About the company

GE Healthcare Systems provides medical technologies and digital infrastructure to improve diagnosis, treatment, and monitoring of patients. Its products include imaging systems, mobile diagnostic devices, patient monitoring tools, and healthcare IT software that work together as hardware, software, and services to support hospitals, clinics, and researchers. The company differentiates itself with a large, integrated ecosystem, strong focus on AI analytics, and a global service network backed by substantial R&D investment. Its goal is to improve patient outcomes and the efficiency of healthcare delivery by enabling accurate diagnoses, effective treatments, and scaled operations.

Company Size

1-10

Company Stage

IPO

Headquarters

Chicago, Illinois

Founded

1892

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Simplify Jobs

Simplify's Take

What believers are saying

  • Q2 2026 orders rose 11% and backlog reached a record $23.9 billion.
  • CareIntellect for Operations launched September 2026 with Duke Health and Queen's Health Systems.
  • CE mark and FDA progress for Photonova Spectra expand 2026-2027 commercial momentum.

What critics are saying

  • FDA logged multiple 2026 Class 2 recalls, including AW Server and telemetry systems.
  • Patient Care Solutions remained weak in Q2 2026; management is reviewing a sale.
  • SOFIE closes only after 2027 regulatory approvals; PET supply integration can slip badly.

What makes GE Healthcare unique

  • GE HealthCare combines imaging hardware, radiopharmaceuticals, and workflow software across hospitals.
  • Photonova Spectra and Vivid 2026 show premium innovation plus AI-enabled clinical automation.
  • SOFIE's 21 cyclotrons extend GE HealthCare into radiotracer manufacturing, not just scanners.

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Benefits

  • Health Insurance
  • Dental Insurance
  • Vision Insurance
  • Life Insurance
  • Disability Insurance
  • 401(k) Retirement Plan
  • 401(k) Company Match
  • Tuition Reimbursement
  • Relocation Assistance

Company News

Associated Press
Oct 20th, 2026
GE HealthCare launches five-institution global trial of StarGuide GX theranostics SPECT/CT system

GE HealthCare has launched a clinical evaluation program for StarGuide GX, its next-generation digital 4D SPECT/CT system. Five institutions across three continents will take part. They are Hadassah Medical Center and Rambam Health Care Campus in Israel, Mayo Clinic in the US, Oncopole Claudius Regaud in France, and Peking University First Hospital in China. Each will assess image quality, quantitative performance, dynamic imaging, and workflow, and give feedback to guide the system's development. StarGuide GX uses dual-sided cadmium zinc telluride detectors and a dual-collimator design meant to remove manual collimator changes. It also uses NVIDIA RTX accelerated computing for image reconstruction. The system received CE Mark in November 2025 and is on sale in select EU states. Its US Food and Drug Administration 510(k) clearance is pending.

Yahoo Finance
Oct 19th, 2026
GE HealthCare launches LOGIQ Focus ultrasound with AI tools, 26% faster scans

GE HealthCare has launched LOGIQ Focus, a new general imaging ultrasound system in its LOGIQ family. The company announced the product in Chicago on October 19, 2026. The system runs on cSound Architecture and pairs high-definition imaging with AI-enabled tools. One of them, Auto Preset Assistant, detects the anatomy being scanned and activates the matching preset, saving up to five clicks per exam. In a third-party study, 90% of participants rated its image quality as excellent. The system was 26% faster than the predicate system. LOGIQ Focus is 510(k) cleared and CE Marked. GE HealthCare expects it and several other new products to add 1% to 2% to revenue growth, following more than $5 billion in innovation investment since 2023.

Business Wire
Oct 5th, 2026
GE HealthCare to acquire SOFIE Biosciences for $945M to expand US radiopharmaceutical supply

GE HealthCare has agreed to acquire SOFIE Biosciences, a US-based contract manufacturer of PET radiopharmaceuticals, for $945 million in cash. The deal with seller Trilantic North America is expected to close in the first half of 2027, subject to regulatory approvals. SOFIE Biosciences operates 15 contract manufacturing sites with 21 cyclotrons across the US, plus a theranostics-focused development and manufacturing facility. The acquisition establishes GE HealthCare's presence in the time-critical "final mile" of US PET radiopharmaceutical supply. The PET radiopharmaceutical market is expanding rapidly with approximately 20 PET radiotracers and over 30 radiotherapeutics currently under development. SOFIE Biosciences' portfolio includes a Phase III FAPI asset for which GE HealthCare already holds non-US rights. GE HealthCare estimates the transaction will be accretive to revenue growth, earnings margin, and earnings per share in the first full year of ownership.

PR Newswire
Sep 30th, 2026
AsiaMedic first in ASEAN to deploy GE HealthCare's MR31 deep learning MRI platform

AsiaMedic has become the first site in ASEAN to implement MR31, GE HealthCare's latest generation MRI platform featuring deep learning technology. The Singapore-based imaging centre is among the earliest adopters in Asia Pacific. MR31 incorporates deep learning technologies that reduce scan times and enable detailed examinations across neurological, musculoskeletal and nerve imaging. Sonic DL for 3D delivers up to 12 times scan acceleration, reducing examination times across brain, spine, orthopaedic and body scans. The platform also supports high-quality prostate MRI imaging. AIR Recon DL Phase Correction provides improved visualisation of clinically significant lesions, whilst high-resolution T2-weighted imaging aids lesion localisation for prostate fusion biopsy planning. Shorter scan times mean reduced patient time in scanners and may help decrease repeat examinations caused by movement.

Associated Press
Sep 22nd, 2026
GE HealthCare raises quarterly dividend 14% to $0.04 per share for Q3 2026

GE HealthCare Technologies announced a 14% dividend increase for the third quarter of 2026. The company's board declared a cash dividend of $0.04 per share, up from the previous quarter. The dividend will be paid on 13 November 2026 to shareholders of record as of 23 October 2026. GE HealthCare is a global healthcare solutions provider specialising in medical technology, pharmaceutical diagnostics, and AI-enabled software solutions. The company operates a $20.6 billion business with approximately 54,000 employees worldwide, serving the healthcare industry through its Advanced Imaging Solutions, Pharmaceutical Diagnostics, and Patient Care Solutions segments.