Senior Medical Device Regulatory Policy Lead
Hybrid (Bengaluru)Posted 1w ago
About the role
Senior Regulatory Policy Specialist role focused on driving Google’s advocacy in India for medical device features, coordinating with Indian health authorities and cross-functional teams to translate global health policy into proactive product guidance for safe, compliant market access.
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.
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, and monitoring regulatory developments and composing authoritative policy briefs.
- Experience leading government agency engagement outside of submission advocacy strategies and educating 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.
Skills
Required:Regulatory affairs in medical devicesGovernment engagement and stakeholder managementCross-functional collaboration
Last updated Oct 23, 2026. Interested? Apply on the company site.
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