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GE Healthcare

Imaging, monitoring, and healthcare IT solutions

Lead Analytical Scientist

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeOslo, NorwayNo salary listedIn-person

About the Job

Requirements

  • A Ph.D. or M.Sc. in Analytical Chemistry, Pharmaceutical Sciences, Chemistry, or a related scientific discipline, with relevant industry experience.
  • Extensive hands-on experience with HPLC method development, optimization, validation, verification, transfer, and lifecycle management.
  • Strong practical experience with HPLC-UV, chromatographic data systems, system troubleshooting, and analytical sample preparation.
  • Strong scientific judgement, structured problem-solving skills, experience interpreting complex analytical data, and ability to prepare clear scientific and technical documentation.
  • Ability to work effectively in a multidisciplinary and time-sensitive environment.
  • Fluency in English, both written and verbal.

Responsibilities

  • Serve as the laboratory-based Analytical Chemistry subject matter expert for control methods supporting Molecular Imaging agents.
  • Develop, optimize, and validate HPLC-UV and HPLC-radiometric methods for Molecular Imaging agents in the new product introduction pipeline.
  • Provide hands-on troubleshooting of chromatographic methods, instrumentation, sample preparation, and analytical investigations.
  • Plan and support method transfer, verification, and implementation within internal and external receiving laboratories.
  • Author and review analytical procedures, protocols, development and validation reports, transfer documentation, investigation reports, and regulatory-supporting documents.
  • Communicate analytical results, risks, and recommendations to cross-functional project teams and contribute to control strategy decisions.
  • Contribute to standardized working practices, technical capability building, and continuous improvement within Analytical Chemistry.

Desired Qualifications

  • Experience supporting radiopharmaceutical or Molecular Imaging product development and manufacture, especially with HPLC coupled to radiometric detection, including gamma-detection systems.
  • Hands-on experience with liquid chromatography-mass spectrometry, mass-spectral interpretation, and impurity characterization.
  • Experience working under good manufacturing practice/good practice (GMP/GxP) or within an accredited laboratory.
  • Knowledge of applicable International Council for Harmonisation and regulatory expectations for analytical methods across the pharmaceutical development lifecycle.
  • Fluency in Norwegian, or willingness to learn if based in Oslo.

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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