Technical Program Manager, Medical Devices
VerilyAbout the role
Who We Are
Verily is a subsidiary of Alphabet that is using a data-driven approach to change the way people manage their health and the way healthcare is delivered. Launched from Google X in 2015, Our purpose is to bring the promise of precision health to everyone, every day. We are focused on generating and activating data from a variety of sources, including clinical, social, behavioral and the real world, to arrive at the best solutions for a person based on a comprehensive view of the evidence. Our unique expertise and capabilities in technology, data science and healthcare enable the entire healthcare ecosystem to drive better health outcomes.
Description
We are looking for an experienced Technical Program Manager to bring novel medical devices from concept through development to formal release. This includes managing project schedules, identifying and mitigating risks, managing the Design History File and building alignment with project stakeholders. You're equally at home working alongside Quality and Regulatory to identify and evaluate hazards as you are discussing the technical trade-offs in product development with engineers, or ways to enhance the product experience with the UX team
The most successful candidate for the role will have strong technical aptitude for medical or other regulated products with integrated hardware and software. Prior experience will include significant hands-on technical work (through product release) and experience working with Engineering, Operations, Clinical, Quality and Regulatory teams to enable successful product deployments.
Responsibilities
- Provide the required hands-on project management of major technical deliverables, cross-functional coordination, and inter/intra team communications to deliver outstanding program and product outcomes.
- Manage complex schedules that involve large, cross-functional teams. Multi-task and prioritize activities for quick execution of critical path work items.
- Ensure product development activities align with technical specifications, and that teams rely on data to create the best research and development concepts and products.
- Collaborate with internal organizations (Manufacturing, Quality, Regulatory, Clinical, Legal, User Success) to enable complex product releases and drive quality through every step of the product development lifecycle.
- Use your technical background to contribute to technical design and implementation as well as triage and resolve complex system issues.
Qualifications
Minimum qualifications:
- BA/BS degree in technical field, or equivalent practical experience.
- 5+ years of technical program management experience, from concept through commercialization.
- Direct experience working with devices in a medical regulated industry.
- Excellent communication and project management skills, with a track record of handling multiple programs and streams of work.
Preferred qualifications:
- Master's degree in a technical field.
- Experience with medical device development standards e.g. ISO 13485, FDA 21 CFR 820.
- Experience working with products incorporating hardware, firmware and software.
- Taken medical devices from prototype to commercial release.
- Ability to contribute to technical discussions, especially in the systems architecture and validation domains, and exercise technical and product judgment to independently resolve project issues.
The US base salary range for this full-time position is $129,000-$199,000 + bonus + equity + benefits. Our salary ranges are determined by role, level, and location. The range displayed on each job posting reflects the minimum and maximum target for new hire salaries for the position across all US locations. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. Your recruiter can share more about the specific salary range for your preferred location during the hiring process.
Please note that the compensation details listed in US role postings reflect the base salary only, and do not include bonus, equity, or benefits.
Why Join Us
Build What’s Vital.
At Verily, you are a part of something bigger. We are a diverse team of builders innovating at the intersection of health and technology—united by a shared spirit of curiosity, resilience and determination to make better health possible for all. This builder mindset means your fingerprints will be on the work that shapes the future of health. Fulfilling our precision health purpose starts with the health of our Veeps (what we
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