Senior Medical Device Regulatory Policy Lead

Google; Gurugram District; Hybrid; INR 4,000,000 - 7,000,000; Full time

Job summary

Google in India is seeking a Senior Regulatory Policy Specialist to drive advocacy for medical device features and AI policy. You will build executive relationships with health authorities and translate policy into product guidance.

Collaborate with Clinical, Engineering, and Government Affairs to ensure compliance and accelerate market access while representing Google's positions in industry coalitions and standards bodies.

Qualifications

• Master's degree in Science, Engineering, Software, Law, Public Health, Public Policy, or related field, or equivalent practical experience.
• 8 years of professional experience in regulatory affairs.
• Experience with medical device standards and SaMD frameworks.
• Lead government agency engagement beyond submission advocacy strategies.
• Collaborate cross-functionally with clinical, quality, and engineering teams to align product strategy with regulatory requirements.

Responsibilities

• Coordinate engagements with Indian health authorities such as the CDSCO and represent Google's regulatory positions at high-level meetings.
• Monitor India’s regulatory developments related to digital health, healthcare AI, and SaMD.
• Represent Google across industry associations and standards bodies to build policy coalitions.
• Liaise with internal teams to align device feature claims with evidence and support India marketing authorizations.
• Provide regulatory policy counsel to leadership and harmonize India policy with global launches.

Skills

Regulatory affairs

SaMD standards

Cross-functional collaboration

Policy advocacy

Stakeholder engagement

Education

Master's degree or equivalent

Job description

Note: By applying to this position you will have an opportunity to share your preferred working location from the following: Bengaluru, Karnataka, India; Gurugram, Haryana, India.

Minimum qualifications:

• Master's degree in Science, Engineering, Software, Law, Public Health, Public Policy, a related field, or equivalent practical experience.
• 8 years of professional experience in regulatory affairs.
• Experience with medical device standards and Software as a Medical Device (SaMD) frameworks, and monitoring regulatory developments and composing authoritative policy briefs.
• Experience to lead government agency engagement outside of submission advocacy strategies and educate global health authorities on modern oversight frameworks for AI.
• Experience working cross-functionally with clinical, quality, and engineering teams to align product strategy with regulatory requirements.

Preferred qualifications:

• Experience in engaging with Regulatory agencies outside of submission.
• Experience within digital health or AI policy and understanding of generative models in clinical settings.
• Previous participation and proven effectiveness in international regulatory/industry forums/standards organizations.
• Track record of contributing to international standards (ISO/IEC, AAMI).

About the job

As a Senior Regulatory Policy Specialist reporting directly to the Senior Director of Digital Health Strategy, you will help drive Google’s advocacy in India for medical device features. Serving as an essential partner and a catalyst, you will facilitate executive-level agency relationships, prepare leadership for high-level engagements, and represent company technical positions in industry coalitions, public consultations, and standards bodies. Additionally, you will collaborate closely with internal stakeholders across Clinical, Engineering, and Government Affairs to translate evolving global health policy into clear, proactive product guidance that accelerates safe, compliant market access.

Google for Health is a company-wide effort to help billions of people be healthier. We work toward this direction by meeting people in their everyday moments and empowering them to stay healthy and partnering with care teams to provide more accurate and accessible care. Our teams are applying our 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 the screening and diagnosis of disease, and data and insights to the public health community.

Responsibilities

• Coordinate and facilitate engagements with Indian health authorities such as the CDSCO, supporting leadership during high-level meetings and representing Google's regulatory positions where executive presence is needed.
• Monitor and analyze India’s legislative, statutory, and medical device regulatory developments related to digital health, healthcare AI, and Software as a Medical Device (SaMD).
• Represent Google across key India industry trade associations and standards bodies, including CTA Health, WHO-India, APAC med, and ISO committees, and other advocacy groups to build collaborative policy coalitions..
• Liaise with internal engineering, clinical, quality, and government affairs teams to align device feature claims with necessary clinical evidence and support India marketing authorizations.
• Provide regulatory policy counsel to leadership and collaborate with regional leads to ensure India policy initiatives harmonize with global digital health launches.

Google is proud to be an equal opportunity workplace and is an affirmative action employer. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status. We also consider qualified applicants regardless of criminal histories, consistent with legal requirements. See also Google's EEO Policy and EEO is the Law. If you have a disability or special need that requires accommodation, please let us know by completing our Accommodations for Applicants form .