Manager, Regulatory Affairs – Global Labeling, PDx

MS0230 GE Healthcare Inc.; United States; Teletrabalho; USD 106 000 - 160 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

401(k) plan with company contributions

Life, disability, and accident ins.</

Tuition reimbursement

Paid time off

Resumo da oferta

GE HealthCare is seeking a Manager, Regulatory Affairs – Global Labeling to develop and execute global labeling strategies, with a primary focus on US FDA labeling and USPI updates. The role partners with Clinical, CMC, Safety, Medical, Commercial, and global/regional Regulatory Affairs to ensure labeling is scientifically sound and globally aligned.

You will lead labeling updates, support FDA interactions, and coordinate CCDS alignment across markets while driving governance and continuous

Qualificações

• 7+ years of Regulatory Affairs experience with labeling expertise.
• Strong knowledge of FDA labeling requirements and US regulatory submissions.
• Experience maintaining US labeling and/or CCDS.

Responsabilidades

• Lead global labeling strategy with focus on US FDA labeling requirements.
• Provide labeling input to development programs and regulatory submissions.
• Ensure alignment between US labeling, CCDS, and regional plans.
• Lead preparation and review of US labeling content and FDA interactions.
• Collaborate with cross-functional teams to support labeling decisions.
• Maintain labeling governance, tracking, and inspection readiness.

Conhecimentos

Regulatory affairs

FDA labeling

Cross-functional collaboration

Communication

Formação académica

Life Sciences/Pharmacy degree

Ferramentas

Veeva RIM

Descrição da oferta de emprego

Job Description Summary The Manager, Regulatory Affairs – Global Labeling is responsible for developing and executing global labeling strategies for assigned PDx products, with primary accountability for US FDA labeling activities and US Prescribing Information. The role partners with Clinical, CMC, Safety, Medical, Commercial, global Regulatory Affairs and regional Regulatory Affairs teams to ensure labeling is scientifically sound, globally aligned, and supports product development, registration, lifecycle management, and commercialization.

Key Responsibilities

Global Labeling Strategy Lead global labeling strategy for assigned products, with primary focus on US FDA requirements and labeling expectations.

Provide labeling input to development programs, lifecycle management activities, and regulatory submissions.

Ensure alignment between US labeling, CCDS, and regional implementation strategies.

FDA Labeling Leadership Lead preparation and review of US labeling content, including USPI and FDA labeling updates. Support FDA interactions and labeling negotiations. Assess regulatory risks and communicate the impact of FDA feedback on development and commercialization plans.

Cross-Functional Collaboration Partner with Clinical, CMC, Safety, Medical, Market Access, Commercial, Legal, and Ad Promo teams to develop clear and defensible labeling positions. Translate complex regulatory requirements into business-relevant recommendations.

Governance & Compliance Support labeling governance processes and ensure inspection-ready documentation. Drive timely implementation of labeling changes and continuous process improvement. Contribute to labeling metrics, systems, and best practices across the organization.

CCDS Alignment & Global Implementation Support CCDS creation, maintenance, version control, and change-control activities, ensuring US labeling decisions are assessed for global impact and properly reflected in global labeling governance. Coordinate with global regulatory leads and regional RA teams to evaluate local implementation requirements, document deviations or exceptions from CCDS, and maintain transparent rationale for regional differences. Track implementation of labeling changes across US and global markets, including milestones, dependencies, approvals, exceptions, and closure status. Maintain labeling trackers, action logs, decision records, and implementation status to support global visibility and inspection readiness.

Required Qualifications

7+ years of Regulatory Affairs experience, including significant experience in labeling. Strong knowledge of FDA labeling requirements and experience supporting US regulatory submissions. Experience developing and maintaining US labeling and/or CCDS. Ability to influence cross-functional teams and manage complex projects. Excellent written and verbal communication skills.

We will not sponsor individuals for employment visas, now or in the future, for this job opening.

Preferred Qualifications

Experience interacting with FDA on labeling matters. Knowledge of EU and global labeling requirements. Experience with Veeva RIM or similar regulatory systems. Degree in Life Sciences, Pharmacy, or related field.

For U.S. based positions only, the pay range for this position is $106,400.00-$159,600.00 Annual. It is not typical for an individual to be hired at or near the top of the pay range and compensation decisions are dependent on the facts and circumstances of each case. The specific compensation offered to a candidate may be influenced by a variety of factors including skills, qualifications, experience and location. In addition, this position may also be eligible to earn performance based incentive compensation, which may include cash bonus(es) and/or long term incentives (LTI).

GE HealthCare offers a competitive benefits package, including not but limited to medical, dental, vision, paid time off, a 401(k) plan with employee and company contribution opportunities, life, disability, and accident insurance, and tuition reimbursement.

Additional Information

Relocation Assistance Provided: No

At GE HealthCare, we see possibilities through innovation. We’re partnering with our customers to fulfill healthcare’s greatest potential through groundbreaking medical technology, intelligent devices, and care solutions. Better tools enabling better patient care. Together, we are not only building a healthier future but living our purpose to create a world where healthcare has no limits.

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). While GE HealthCare does not currently require U.S. employees to be vaccinated against COVID-19, some GE HealthCare customers have vaccination mandates that may apply to certain GE HealthCare employees.