Director of Regulatory Affairs - Remote

UnitedHealth Group•Eden Prairie, MN

2d•$134,600 - $230,800•Remote

About The Position

The Director of Regulatory Affairs will be a member of the Legal Team responsible for providing the enterprise with strategic counsel and support on regulatory and quality matters related to medical devices, including software and algorithms, and other digital health technologies. As a subject matter expert and leader, the Director of Regulatory Affairs will play a key role in developing and optimizing our regulatory affairs team, programs, and services. The Director of Regulatory Affairs will be responsible for maintaining and continuously improving enterprise regulatory affairs policies and procedures. Working closely with their team, legal and compliance colleagues, and business stakeholders, the Director of Regulatory Affairs will lead or support a wide range of regulatory activities, including regulatory assessments for new product/therapies and changes to existing products and the development and the execution of regulatory plans/strategies as required. You’ll enjoy the flexibility to work remotely from anywhere within the U.S. as you take on some tough challenges. For all hires in the Minneapolis or Washington, D.C. area, you will be required to work in the office a minimum of four days per week.

Requirements

10+ years of experience in medical device regulatory affairs or related field
Proven experience in preparing and submitting regulatory documentation including filings to the FDA, EU MDR, and/or other global regulatory agencies
Experience with completing or supporting regulatory compliance activities like site registrations, audits, post-market vigilance reporting, and product recalls
Demonstrated familiarity using and/or managing electronic quality management systems
Proven expertise and working knowledge of applicable regulations, standards and guidance for medical devices (FDA, QSMR, SaMD, ISO 13485, ISO 14971, IEC 62304, and other global regulatory requirements and quality standards)
Proven ability to learn and adapt to provide strategic regulatory advice in an evolving industry
Proven excellent written and oral communication, interpersonal, and problem-solving skills to effectively interact with others, including cross-functional teams and regulatory agencies, and address regulatory matters
Demonstrated ability to successfully manage multiple regulatory projects, priorities, and people, if relevant

Nice To Haves

J.D., RAC Certification, ISO 13485 or other medical device auditor certification
Direct experience with Software as a Medical Devices (SaMD), other Digital Health products, and accessories
Direct experience with AI/ML-enabled medical devices or digital health technology

Responsibilities

Lead and draft, review, and provide guidance on regulatory product assessments and other deliverables
Prepare regulatory plans/strategies and provide ongoing support as needed for various regulatory, quality, and compliance activities
Provide expert and practical regulatory advice and support on regulatory and quality requirements throughout a project or product lifecycle
Effectively communicate complex regulatory topics to a broad audience in our enterprise and collaborate across the enterprise to successfully strategize and achieve regulatory and quality objectives
Review and provide guidance on labeling including promotional labeling and advertisements (promotional communications)
Collecting, analyzing, and disseminating regulatory intelligence on new and changing requirements, policies, and guidelines
Support regulatory compliance activities, including manufacturing site registration, audits, inspections, post-market vigilance reporting, and product recalls
Prepare or support regulatory submissions and filings as needed
Develop and present educational and training material covering medical device and digital health regulatory affairs topics
Manage and participate in trade associations covering medical device topics and issues