Quality Lead Specialist - Regulatory Affairs

Job Description Summary Provides regulatory strategy and direction to the business regarding healthcare industry regulatory requirements for product launches, premarket submissions/registrations, and postmarket compliance, working closely with global healthcare regulatory bodies. Demonstrates an in-depth understanding of key business drivers and uses this knowledge to accomplish assigned work. Exhibits a strong understanding of how the team’s work integrates with other functions and contributes to the broader organization. Roles and Responsibilities Provides regulatory strategy and direction to the business regarding healthcare industry regulatory requirements for product launches, premarket submissions/registrations, and postmarket compliance, while collaborating with global healthcare regulatory bodies. Develops in-depth expertise within the discipline; applies prior experience and acquired knowledge to execute functional policy and strategy. Typically operates as an individual contributor with strong interpersonal skills. Communicates with colleagues and the business regarding design and coordination activities. Provides informal guidance to new team members and explains complex information in straightforward scenarios. Impacts projects, processes, and procedures within own field. Operates with some autonomy, focusing on execution and the provision of guidance within established functional practices and procedures. Activities require professional judgment and may involve occasional guidance from more senior team members. Utilizes technical expertise and judgment to solve problems. Applies analytical thinking and leverages multiple internal resources, including those outside the immediate team, to support decision-making. Qualifications Bachelor’s degree from an accredited university or college or a high school diploma/GED with at least 6 years of experience in the relevant job family/function. Strong oral and written communication skills. Demonstrated ability to analyze and resolve problems. Ability to document, plan, market, and execute programs. Established project management skills. Legal and Eligibility To comply with U.S. immigration and other legal requirements, it is necessary to specify the minimum number of years of experience required for roles based in the United States. For roles outside of the USA, job descriptions should focus on the substantive level of experience required rather than specifying a minimum number of years. We will not sponsor individuals for employment visas, now or in the future, for this job opening. Benefits and Work Environment 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 #J-18808-Ljbffr HC1316 GE Precision Healthcare LLC