Senior Medical Device Regulatory Policy Lead
Google · Bangalore
Collected role description
Role overview
Senior Medical Device Regulatory Policy Lead at Google
Required qualifications
- Minimum qualification: 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 and skills
- Preferred qualification: 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).
Employment details
- Location: Bengaluru [Karnataka] [India]
Application details
- Information collected and processed as part of your Google Careers profile, and any job applications you choose to submit is subject to Google's Applicant and Candidate Privacy Policy .
About the employer
- Google is proud to be an equal opportunity and affirmative action employer.
- Google is a global company and, in order to facilitate efficient collaboration and communication globally, English proficiency is a requirement for all roles unless stated otherwise in the job posting.
- Please do not forward resumes to our jobs alias, Google employees, or any other organization location.
Additional role details
- We are committed to building a workforce that is representative of the users we serve, creating a culture of belonging, and providing an 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 .
- To all recruitment agencies: Google does not accept agency resumes.
- 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.
Collected minimum qualification
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.
Collected preferred qualification
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).
Collected experience requirement
8 years of professional experience in regulatory affairs.