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The Senior Director leads global Notified Body engagement, certification strategy, and audit governance to ensure regulatory compliance across GE HealthCare. They also oversee QMS integration assessments for mergers and acquisitions while providing strategic guidance to executive leadership.
Roles and Responsibilities
Represents GE HealthCare to Notified Bodies, certification bodies, auditing organizations, and external regulatory stakeholders, establishing strategic relationships that support certification activities, regulatory compliance, and business objectives.
Owns the enterprise strategy for Notified Body engagement and certification management, including certification transfers, scope expansions, site additions, legal entity changes, remediation strategies, and certification pathway planning.
Provides strategic oversight and governance of Notified Body audits, technical documentation assessments, surveillance audits, recertification audits, and unannounced audits, including risk assessment, escalation management, and issue resolution. Develops, standardizes, and continuously improves tools and standard work supporting Notified Body engagement.
Serves as the primary point of contact between GE HealthCare and Notified Bodies, driving contract negotiations and resolving certification, compliance, capacity, and service-related concerns.
Leads QMS post-acquisition integration assessments for acquisitions, mergers, divestitures, and business expansions, including compliance evaluations, certification impact assessments, and supporting integration planning.
Generates metrics, trend analyses, executive dashboards, and leadership presentations related to audit performance, certification status, compliance risks, Notified Body effectiveness, and QMS integration activities.
Leads through complexity by managing competing priorities across regions, business units, product lines, and regulatory frameworks while building consensus among internal and external stakeholders.
Required Qualifications
Master’s degree and a minimum of 10 years’ experience in the medical device industry; or bachelor’s degree and a minimum of 15 years’ experience in the medical device industry.
Demonstrated understanding of Medical Device QMS and regulatory requirements including but not limited to FDA CFR 21 820, EU MDR, MDSAP and ISO 13485.
Minimum 5 years of progressive Quality and/or Regulatory Affairs experience at a GE HealthCare site, with demonstrated responsibility for supporting or leading interactions with Notified Bodies during audits, certifications, surveillance activities, technical reviews, or compliance-related engagements.
Demonstrated experience developing metrics, analyzing quality or regulatory data, identifying trends, and preparing executive-level communications or presentations to support decision-making.
Demonstrated expertise communicating across all levels of the organization on design controls, design verification and validation, production and process controls, CAPA, complaints, risk management, certification strategy, and regulatory compliance expectations.
Excellent written and verbal communication skills in English, with a demonstrated commitment to integrity, ethical decision-making, and professional conduct.
Desired Characteristics
Demonstrated understanding of medical device and quality management system certification programs, including EU MDR, MDSAP, ISO 13485, ISO 9001, UKCA, legal entity considerations, and certification management strategies.
Experience working directly with Notified Bodies, certification bodies, auditing organizations, regulators, or external regulatory stakeholders in a global medical device environment including managing certification portfolios, Notified Body relationships, contract negotiations, service expectations, and associated budgets.
Demonstrated ability to influence organizational strategy and drive alignment across global functions, business units, sites, executive leaders, and external stakeholders.
Strong analytical, problem-solving, and root cause analysis skills, with the ability to manage multiple priorities, interpret technical documentation, convert data into actionable insights, and communicate risks clearly.
Ability to travel domestically and internationally up to 20%.
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
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