Medical Device Regulatory Specialist

## Benefits Package
In accordance with Washington state law, we are highlighting our comprehensive benefits package, which is available to all eligible US‑based employees. Benefits for this role include:

– Health, dental, vision, life, disability insurance
– Retirement Benefits: 401(k) with company match
– Paid Time Off: 20 days of vacation per year, accruing at a rate of 6.15 hours per pay period for the first five years of employment
– Sick Time: 40 hours/year (increased to 69 hours/year for Seattle), including 5 discretionary sick days per instance
– Maternity Leave (Short‑Term Disability + Baby Bonding): 28–30 weeks
– Baby Bonding Leave: 18 weeks
– Holidays: 13 paid days per year

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## Minimum Qualifications
– Master’s degree in Engineering, a related technical field, or equivalent practical experience.
– 5 years of experience in regulatory affairs and engagement with global regulatory bodies.
– Experience with medical device standards and Software as a Medical Device (SaMD) frameworks.
– Experience monitoring regulatory developments and composing white papers or policy briefs.

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## Preferred Qualifications
– Experience at leading med‑tech firms, having served as the Directly Responsible Individual (DRI) for innovative product launches.
– Experience within digital health or AI policy space, including deep understanding of how generative models are integrated into clinical settings.
– Familiarity with Cloud‑native Quality Management Systems (ISO 13485) and AI‑specific quality standards (ISO 42001).
– Deep understanding of international harmonization efforts such as IMDRF and the processes regulators use to develop policy and guidance in major markets like the US and EU.
– Proven track record of contributing to the creation of international standards through organizations such as ISO/IEC and AAMI.

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## About the Job
The Digital Health Regulatory Quality and Strategy (DHRQS) team serves as the advisors helping Google navigate the complex and evolving global health regulatory landscape. Our team is at the forefront of defining how AI can safely and effectively transform healthcare.

We focus on three primary pillars:
1. Providing regulatory strategy and operational infrastructure to help product teams across Google build and launch regulated products globally.
2. Safeguarding Google’s core platforms and general‑purpose models from being unintentionally regulated or exposed to liability, ensuring a clear separation between regulated features and core business services.
3. Actively partnering with global health authorities to shape international standards and national policies, ensuring AI regulations balance innovation with safety.

In this role, you will operate at the nexus of the health ecosystem, technological advancement, and regulatory expertise to steer Google’s platforms in supporting billions of individuals throughout their health experiences. You will work with engineers, product builders, and clinicians who are passionate about applying technology in health.

Google for Health is a company‑wide effort to help billions of people be healthier. We work toward this vision by meeting people in their everyday moments, empowering them to stay healthy, and partnering with care teams to provide more accurate and accessible care. Our teams apply expertise and technology to improve health outcomes globally — with high‑quality information and tools to help people manage their health and wellbeing, solutions to transform care delivery, research to catalyze the use of artificial intelligence for screening and diagnosis, and data and insights for the public health community.

Individual pay is determined by factors including job‑related skills, experience, and relevant education or training.

**US Compensation:**
$144,000 – $209,000 (USD) + 15% bonus target + equity + benefits

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## Responsibilities
– Monitor and analyze legislative and regulatory developments related to AI and healthcare policy. Coordinate and facilitate professional regulatory engagements with regulators and policymakers and prepare formal submissions.
– Maintain expertise regarding emerging regulatory frameworks as they pertain to Medical Devices and Software as a Medical Device (SaMD).
– Liaise with engineering and clinical functions at Google to align regulatory claims with necessary evidence. Provide support to Leadership during high‑level meetings with regulators and contribute to international standards development.
– Conduct comprehensive monitoring and analysis of legislative and regulatory shifts in AI and healthcare policy.
– Compose authoritative white papers, policy briefs, and participate in formal responses to public consultations initiated by regulatory entities or standards development organizations.

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## Equal Opportunity Statement
Google is proud to be an equal opportunity and affirmative action employer. We are committed to building a workforce that is representative of the users we serve, creating a culture of belonging, and providing equal employment opportunity regardless of race, creed, color, religion, gender, sexual orientation, gender identity/expression, national origin, disability, age, genetic information, veteran status, marital status, pregnancy or related condition (including breastfeeding), expecting or parents‑to‑be, criminal histories consistent with legal requirements, or any other basis protected by law.

See also Google’s EEO Policy, Know Your Rights: Workplace Discrimination Is Illegal, Belonging at Google, and How We Hire.

If you have a need that requires accommodation, please let us know by completing our Accommodations for Applicants form.

Google is a global company and, to facilitate efficient collaboration and communication globally, English proficiency is a requirement for all roles unless stated otherwise in the job posting.

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## Additional Information
To all recruitment agencies: Google does not accept agency resumes. Please do not forward resumes to our jobs alias, Google employees, or any other organization location. Google is not responsible for any fees related to unsolicited resumes.

Equity is granted exclusively and discretionarily by Alphabet Inc. on the basis of an agreement concluded between you and Alphabet Inc. Alphabet Inc. is your sole contractual partner with respect to equity grants. GSU grants are not guaranteed, are discretionary, are subject to approval by the Alphabet Inc. board of directors or its delegate, the terms of the relevant Alphabet Inc. stock plan, and your grant agreement. They have no impact on statutory payments. Current or past grants do not confer an acquired right.

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