hirly

Gehc

Regulatory Affairs Manager

Waukesha

See how you match this job — and similar ones. Free.

Upload your resume and hirly scores it against this role at Gehc first, then against similar open jobs, and shows where you fit and why.

PDF or DOCX, up to 12MB. No sign-up to see your matches.

Get past the screening software and onto a recruiter's desk

hirly rewrites your resume for this job — matching the keywords and skills in the posting, moving your most relevant experience to the top, and writing a cover letter to fit. About 30 seconds.

  • Keywords matched to this posting
  • Fit score before you apply
  • Cover letter included

Matched against 2.3M live jobs from 200,000+ employers in 200+ countries.

Tailor my resume for this job →

hirly's read of this role

Seniority
Lead / management
Country
US
Work mode
On-site / unstated
First seen by hirly
27 Sept 2026

Derived automatically from the posting. Upload your resume above to see how the role scores against it.

the posting

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

Original posting on Gehc's site ↗

Want this one?

Upload your resume and hirly rewrites it for this job and writes the cover letter — in about thirty seconds, before you sign up.

Tailor my resume for this job