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General Electric QC Chemistry Project Coordinator in Oslo, Norway

Job Description Summary

The Chem. Quality Control Department, Oslo Site, consists of 24 employees with different background within chemical analysis and GMP Compliance. The department is responsible for the quality control and approval of new materials, in- process and release analysis of aseptic products, in-process and release analysis for the APIs, complaints handling, changes related to the quality aspect for all contrast media and PET products manufactured at the Oslo Site.

As the company is currently growing and developing, QC is looking to improve and strengthen the project team within the QC Chem. organization. We are looking for someone with a background within compliance and analytical chemistry. Your responsibility in this position will include new materials (raw materials, primary packaging, and APIs) that are coming as NPIs into the Oslo Plant and all compliance task related to quality control.

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

Responsibilities

  • Responsible for writing and updating SOPs, protocols, reports, specifications related to NPIs

  • Prioritize tasks from the different projects into the project team and raw material group

  • Responsible for change controls, deviations and CAPAs related to projects

  • Responsible for making sure all established specifications and documentation is in compliance with current regulations as the different pharmacopeias and current GMP regulations.

  • Responsible for writing CoAs when required for projects

Qualifications and experience

  • Bachelors level within Chemistry or equivalent

  • Some experience working in a lab

  • Experience with updating quality documentation

  • Knowledge of method validation

  • Experience in quality control, manufacturing, or quality assurance from the pharmaceutical industry

  • Flexible attitude, work independently, proactive, and responsible

  • Effective time management and organizational skills; able to balance multiple priorities and to work under pressure, accuracy

  • Excellent verbal, and written communications skills, flexible attitude

  • Team player with strong interpersonal skills

  • Norwegian and English language 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.

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.

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Additional Information

Relocation Assistance Provided: No

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