Community

Home >

Jobs >

Regulatory Quality Safety Expert, Google Health

Regulatory Quality Safety Expert, Google Health

1 Month ago • 10 Years + • Quality Assurance

About the job

1 skill required for this role

Test your skills to join the top 1% applicants for this job

risk-management

Job Description

The Regulatory Quality Safety Expert at Google Health partners with teams to ensure product compliance with health regulations and data handling requirements. Responsibilities include navigating regulatory submissions in EMEA for SaMD products, managing applications with regulatory authorities, developing understanding of regional regulations, providing strategic regulatory guidance to stakeholders, collaborating with Google's Government Affairs team, building relationships with industry stakeholders and regulatory bodies, and offering Safety Risk Management expertise to product teams. The role ensures safe, compliant, and timely product launches globally. A strong understanding of SaMD, AI, and relevant global standards (FDA, ISO 13485, ISO 14971, etc.) is crucial.

Must have:

Bachelor's degree in scientific or engineering field
10+ years experience in medical device design quality and safety
Experience with Software as a Medical Device (SaMD)
Regulatory submissions experience
Knowledge of global safety standards and regulations
Safety risk management expertise

Good to have:

Master's degree in scientific or engineering field
Professional certification in Quality, Safety, or Regulatory Affairs
Experience with cloud-based SaMD safety risk assessments
Knowledge of Generative AI and ML models

Minimum qualifications:

Bachelor's degree in a Scientific or Engineering field (e.g., Biomedical Engineering, Life Sciences), or equivalent practical experience.
10 years of experience in design quality and safety risk management in the medical device industry with focus on Software as a Medical Device.
Experience applying medical device requirements to software as a medical device and Artificial Intelligence (AI), including launching and managing the lifecycle of Business-to-Consumer (B2C) Digital Products.
Experience in supporting regulatory audits and Inspections.

Preferred qualifications:

Master’s degree in a Scientific or Engineering field (e.g., Biomedical Engineering, Life Sciences), or equivalent practical experience.
Professional certification in Quality, Safety or Regulatory affairs.
Experience in handling safety risk assessments for cloud based software as medical devices.
Experience with global safety standards and regulations e.g. FDA Quality System Regulation, ISO 13485, ISO 14971, DCB 0129, IEC 62304, AAMI TIR 45 and IEC 62366.
Knowledge of Generative Artificial Intelligence (AI) and Machine Learning (ML) models.
Ability to guide product development teams, navigate regulatory pathways and meet quality/safety standards.

About the job

In this role, you will partner with Googlers to ensure products meet the appropriate health regulations and data handling requirements, and translate quality and safety standards into actionable steps to enable safe, compliant, timely and trusted launches into markets globally. Google's health privacy experts support Privacy Working Groups (PWGs), Counsel and other horizontal teams on complex cases and the operationalization of new health privacy policies.

Google 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 and empowering them to stay healthy and partnering with care teams to provide more accurate, accessible, and equitable 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

Navigate regulatory submissions to various regulatory authorities in Europe, Middle East, and Africa (EMEA) for Software as a Medical Device (SaMD) products. Work with experts and product teams in preparing, submitting, and managing applications, as well as communicate with regulatory authorities.
Develop and maintain an understanding of relevant regional regulations, guidelines, and standards related to SaMD and provide strategic regulatory guidance to internal stakeholders, including Product teams, Clinical Affairs, and Legal teams, on development and commercialization strategies for the region.
Collaborate with Google's Government Affairs team to ensure alignment on strategy and Google’s position in the region.
Build and maintain strong relationships with key industry stakeholders and relevant regulatory bodies in the region.
Provide Safety, Risk Management expertise and guidance to the Product teams, ensuring consistent and accurate application of all Safety Risk Management standards.

View Full Job Description

Upload your resume, increase your shortlisting chances by 80%

About The Company

Google

1890 Active Jobs

A problem isn't truly solved until it's solved for all. Googlers build products that help create opportunities for everyone, whether down the street or across the globe. Bring your insight, imagination and a healthy disregard for the impossible. Bring everything that makes you unique. Together, we can build for everyone.