Jobs › GE HealthCare

This position has closed. GE HealthCare removed this listing from their careers page on Oct 6, 2026. The interview prep below is still useful, and there are similar open roles at the bottom of this page.

Regulatory Affairs Manager

GE HealthCare · Waukesha, WI · Full time

Posted Sep 8, 2026 · We last checked this listing on Oct 5, 2026

Likely interview questions for this role

Written from this job description, not a generic list. Each one notes what the interviewer is really checking.

About your past

Tell me about a submission you led that ran into trouble with a regulator. How did you handle it?

What they are checking: Whether they can manage regulator questions and setbacks while keeping the business informed.

Tell me about a time you influenced a cross-functional team without direct authority.

What they are checking: Whether they can lead by expertise and trust, since regulatory rarely owns the team doing the work.

How do you explain a complicated regulatory risk to a business leader in a few minutes?

What they are checking: Whether they can make regulatory risk clear enough for leaders to make good decisions.

What would you do

Engineering wants to launch on a date your regulatory plan cannot support. What do you do?

What they are checking: Whether they can hold a firm compliance position while offering real options to the business.

How do you handle device classification questions in a market where the rules are unclear?

What they are checking: Whether they can make and defend a reasoned determination and know when to consult the regulator.

About the work

Walk me through how you would build a global regulatory strategy for a new invasive cardiology device.

What they are checking: Whether they can plan US, EU and other market submissions together rather than one country at a time.

How do you decide whether a change to an existing product needs a new 510(k) or a letter to file?

What they are checking: Whether they can apply FDA guidance on device changes with sound, documented reasoning.

How do you review advertising and promotional material for a medical device?

What they are checking: Whether they know claims must match cleared indications and can spot overreach in marketing copy.

What does post-market reporting involve for a cardiology device, and how do you stay on top of it?

What they are checking: Whether they understand complaint, MDR and vigilance duties after a product is on the market.

How do you keep up with regulatory changes like the EU MDR and pass that knowledge to teams?

What they are checking: Whether they practice regulatory intelligence and flow requirements down to engineering.

How do you make sure product labeling stays compliant across many countries?

What they are checking: Whether they have a system for labeling control, since mistakes there cause recalls.

Practice this interview out loud.

Offer builds a real interview for this exact role at GE HealthCare from your resume and this job description, asks the questions one at a time, and tells you what landed. The first one is free.

Practice this out loud

The full job description

As published by GE HealthCare.

Job Description Summary This position provides strategic regulatory leadership for the Invasive Cardiology programs. This includes leading major regulatory projects, programs and regulatory submissions, working closely with a cross-functional team and global regulatory bodies. The Regulatory Affairs Manager will be involved with regulatory activities such as global premarket submissions and registrations, device classifications and determinations, project management, business communication and strategy, risk management, post-market reporting, regulatory intelligence, regulatory requirements flow-down, advertising and promotion review, product labeling compliance, etc. Job Description Roles and Responsibilities • Provides regulatory strategy and direction to the business regarding healthcare industry regulatory requirements for product launch, premarket submissions/registrations and post market compliance, working closely with healthcare regulatory bodies globally • Develops global regulatory strategies, including execution of the regulatory product registrations to support global new product introduction launches. Works closely with cross-functional teams like engineering and product management to drive solutions. • Assesses changes in existing products and determines the need for new / revised licenses or registrations. • Reviews and approves advertising and promotional material to ensure consistency with approved claims and regulatory requirements. • Leads regulatory inspection support, as well as support for regulatory inquiries from authorities related to adverse events or recalls. • Developing specialized depth and/or breadth of expertise in own job discipline or field. Serves as best practice/quality resource. Has awareness of latest functional developments in own area. Contributes towards strategy and policy development, and ensures delivery within area of responsibility. • Skilled influencer, able to communicate complex messages to others. Acts as a resource for colleagues with less experience. May lead small projects with moderate risks and resource requirements. Explains difficult or sensitive information; works to build consensus. Developing persuasion skills required to influence others on topics within field. • Uses judgment to make decisions or solve moderately complex tasks or problems that impact the function. Takes new perspective on existing solutions. Uses technical experience and expertise for data analysis to support recommendations. Uses multiple internal and limited external sources outside of own function to arrive at decisions. Required Qualifications • Bachelor's Degree in a Scientific or Engineering discipline (OR a minimum of 12 years work experience.) • A minimum of 8 years Regulatory Affairs / Quality Assurance experience • A minimum of 8 years experience in the medical device or pharmaceutical industry Desired Characteristics • Strong oral and written communication skills. • Strong interpersonal and leadership skills. • Demonstrated ability to analyze and resolve problems. • Demonstrated ability to lead programs / projects. • Ability to document, plan, market, and execute programs. • Established project management skills. • Advanced degree in scientific, technology or regulatory affairs disciplines • Regulatory Affairs Certification (RAPS) We will not sponsor individuals for employment visas, now or in the future, for this job opening.

 Additional Information 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. Relocation Assistance Provided: No