Global Technical Publication Leader, MR

GE HealthCare • Waukesha, WI

1d • Onsite

About The Position

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. The Global Technical Publication Leader is responsible for the wing-to-wing execution of operator documentation deliverables for Magnetic Resonance (MR) scanner programs. This role ensures that all operator manuals and related documentation meet regulatory, quality, and usability standards, supporting safe and effective system operation by healthcare professionals worldwide. At GE Healthcare, our passionate people are creating the products, solutions and services our customers need to deliver the best patient care possible. Must be able to work onsite daily out of our Waukesha, WI location.

Requirements

• Bachelor’s degree in Biomedical Engineering, or related field; advanced degree preferred.
• 5 years of experience in the medical device industry (MR preferred)
• Strong understanding of MR technology and operator workflows.
• Proven ability to manage complex projects with multiple stakeholders and tight deadlines.
• Software proficiency including Microsoft Office, basic Linux commands, DOORs, and My Workshop applications
• Knowledge of documentation tools and content management systems.
• Excellent communication, leadership, and problem-solving skills

Nice To Haves

• Advanced degree (Masters or PhD).
• At least 8 yrs. experience in the medical industry.
• Knowledge of clinical MR scanning
• Previous GE Healthcare experience.
• Competitive experience.

Responsibilities

• Lead the end-to-end process for operator documentation across MR scanner programs, from planning through release.
• Help define documentation scope, structure, and standards to ensure clarity, compliance, and alignment with product features.
• Partner with engineering, clinical, regulatory, program management, and central OM teams to gather technical inputs and ensure timely delivery.
• Ensure documentation meets global regulatory requirements, internal quality standards, and usability best practices.
• Drive continuous improvement in documentation workflows, tools, and templates to enhance efficiency and consistency.
• Identify and mitigate risks related to documentation deliverables impacting program timelines or compliance.
• Provide regular updates on documentation status, risks, and mitigation plans to program leadership.
• Create and execute validation processes per QMS standards
• Support necessary engineering activities related to product delivery and release

Benefits

• GE HealthCare offers a great work environment, professional development, challenging careers, and competitive compensation.
• GE HealthCare is an Equal Opportunity Employer.
• 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 will only employ those who are legally authorized to work in the United States for this opening.
• Any offer of employment is conditioned upon the successful completion of a drug screen (as applicable).
• Relocation Assistance Provided: Yes

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Number of Employees: 5,001-10,000 employees