VP, Medical Device Engineering

Hims & Hers is the leading health and wellness platform, on a mission to help the world feel great through the power of better health. We are redefining healthcare by putting the customer first and delivering access to care that is affordable, accessible, and personal, from diagnosis to treatment to delivery. No two people are the same, so we provide access to personalized care designed for results. By normalizing health & wellness challenges and innovating on their solutions, we’re making better health outcomes easier to achieve. 

Hims & Hers is a public company, traded on the NYSE under the ticker symbol “HIMS.” To learn more about the brand and offerings, you can visit hims.com/about and hims.com/how-it-works . For information on the company’s outstanding benefits, culture, and its talent-first flexible/remote work approach, see below and visit www.hims.com/careers-professionals.

The VP, Medical Device Engineering will lead the strategy, team, and execution behind our regulated medical device portfolio – building the engineering foundation for a new generation of regulated consumer medical devices designed to make preventative care radically more accessible globally. This is a rare opportunity to shape a world-class device organization, owning everything from early concept through commercialization, while ensuring every product we ship meets the highest bar for safety, quality, compliance, and craftsmanship.

This leader will directly oversee medical device hardware product development and work cross-functionally with Quality, Regulatory Affairs, Clinical, and Manufacturing to bring products from concept to market with speed and rigor.

• Define and execute the strategic roadmap for the regulated devices portfolio, aligned with company growth objectives

• Own budgeting, and resource allocation for the regulated devices business unit • Partner with executive leadership to identify new product opportunities • Build and scale a high-performing, cross-functional organization

• Directly lead R&D developing regulated medical devices from concept through design transfer and commercialization

• Ensure design control processes are robust, compliant, and efficiently executed (21 CFR Part 820, ISO 13485)

• Drive innovation while maintaining disciplined product development processes, including risk management (ISO 14971) and usability engineering

• Ensure all products meet FDA, international regulatory, and quality system requirements

• Partner closely with Quality and Regulatory leaders to support successful submissions (e.g., 510(k), De Novo as applicable)

• Champion a culture of quality and compliance across the organization • Ensure inspection readiness and successful audits (FDA, notified bodies, etc.)

• Provide indirect leadership and alignment across Clinical, Manufacturing, and Supply Chain

• Ensure clinical strategies support regulatory and commercial objectives

• Collaborate with Manufacturing/Operations to ensure scalable, cost-effective, and compliant production processes

• Establish and monitor KPIs across development, quality, regulatory, and manufacturing readiness

• Drive continuous improvement in product development lifecycle, time-to-market, and cost efficiency

• Identify and mitigate technical, regulatory, and operational risks

• Bachelor’s degree in Mechanical Engineering

• 15+ years of experience in the medical device industry, with significant experience in Class II devices

• Proven leadership experience overseeing R&D teams and product development pipelines

• Deep knowledge of FDA regulations, including 21 CFR Part 820, and international standards such as ISO 13485 and ISO 14971

• Demonstrated success leading products through regulatory clearance (e.g., 510(k)) and commercialization

• Experience working closely with Quality and Regulatory functions in a design controlled environment