Find Jobs
Find Jobs Near You – Available Work in Your Location
Skip to job details
GH
GE HealthCare
Regulatory Affairs Leader - ARC
Career Insights for Regulatory Affairs Specialist
See where this job fits in the broader career landscape. Knowing your career path helps you see what's possible from here.
Scorecard
Based on Wisconsin data
Review key factors to help you decide if this role fits your goals. How is this calculated?
What they do
A Regulatory Affairs Specialist maintains specialized knowledge of state and federal government regulations that affect an employer. Interprets regulations and implements procedures that bring an employer into compliance with regulations; may audit internal compliance with regulations.
$82,908 / year median in Wisconsin
+1% projected growth
Job Description
- Job Description Summary
- This position provides strategic regulatory leadership for major regulatory projects, programs and regulatory submissions, working closely with a cross-functional team and global regulatory bodies.
- Job Description
Responsibilities :
1. Provides regulatory leadership and strategic direction for ARC regulatory programs, including global RA support for registration planning, submissions, notified body and quality system audits, and program implementation across a cross-functional team with communication to leadership. Supports compliance of premarket submissions/registrations and post market compliance, working closely with healthcare regulatory bodies globally. 2. Develops regulatory strategies to help optimize regulatory submission pathways, taking into consideration regulatory requirements (including product testing, clinical data, etc), product claims and country regulatory dependencies to ensure optimized sequencing for submissions. 3. Explains information clearly with the right level of detail for the audience, and works to understand a situation, potential risks, and develop possible solutions; brings team members to consensus around topics within the field. 4. Recognizes when additional support from senior levels within RA is needed to ensure sound decisions are made and risks are minimized. 5. Utilizes technical expertise and judgement to solve problems. Leverages technical skills and analytic thinking required to solve problems. May use multiple internal sources outside of own team to arrive at decisions. 6. Assesses changes in existing products and determines the need for new / revised licenses or registrations. 7. Reviews and approves advertising and promotion material to ensure consistency with approved claims and regulatory requirements. 8. Contributes to writing and editing technical documents 9. Researches, analyzes, integrates and organizes background information from diverse sources for regulatory submissions 10. Understands and applies regulatory requirements and their impacts for submissions and pre- and post-market compliance.Qualifications :
1. This role requires advanced experience in the Quality & Regulatory Affairs. Knowledge level is comparable to a Bachelor's degree from an accredited university or college. 2. Minimum of 3 years experience working in a regulated field 3. Strong communication skills in English (both written and oral).Characteristics :
1. Strong communication, project management, and organizational skills 2. Ability to work independently in fast-paced environment and adapt to change. 3. Has ability to prioritize information for data analysis and recognize when additional information and support is needed. 4. Team-oriented and responsive to customer needs. 5. Attention to Detail and Results-Oriented. 6. Ability to understand technical documentation and execute associated procedures- Inclusion and Diversity
- GE HealthCare is an Equal Opportunity Employer where inclusion matters.
- Additional Information
Relocation Assistance Provided:
- No