Senior Program Manager, SaMD

Posted Yesterday
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Boston, MA, USA
Hybrid
155K-185K Annually
Senior level
Fitness • Hardware • Healthtech • Sports • Wearables
Power your performance with 24/7 data
The Role
Drive end-to-end execution of Software as a Medical Device programs from development through regulatory submission and launch. Coordinate Product, Engineering, Machine Learning, Clinical, Regulatory, and Quality stakeholders; manage plans, dependencies, risks, milestones, verification and validation, clinical studies, regulatory preparation, and design history documentation. Strengthen program management processes while ensuring compliance with design controls, quality systems, and applicable medical device standards.
Summary Generated by Built In

WHOOP is an advanced health and fitness wearable on a mission to unlock human performance. We empower our members to improve their health and perform at a higher level through a deeper understanding of their bodies and daily lives.

We are looking for a Senior Program Manager, SaMD to join our growing team and help scale the execution of our Software as a Medical Device programs. This role will partner closely with an existing Program Manager and cross-functional leaders to drive the successful delivery of regulated features.

This is an execution-focused role for someone who has experience working on end-to-end SaMD programs and can operate effectively within an established but evolving system.

RESPONSIBILITIES:

  • Drive execution of SaMD programs across the full product lifecycle, from development through regulatory submission and launch

  • Partner with Machine Learning, Product, Engineering, Clinical, Regulatory, and Quality to plan and deliver against program milestones

  • Work alongside an existing Program Manager to coordinate multiple SaMD initiatives, ensuring alignment across timelines and dependencies

  • Build and maintain detailed program plans, tracking progress against key deliverables and identifying risks early

  • Support development in compliance with design controls and regulatory requirements, ensuring documentation and processes are followed

  • Coordinate cross-functional activities including: Verification & validation, Clinical studies, Regulatory submission preparation, Design history file (DHF) documentation

  • Identify and proactively manage program risks and blockers, escalating as needed

  • Facilitate clear and consistent communication across stakeholders, including regular program updates

  • Help strengthen and scale program management processes as WHOOP expands its SaMD portfolio

QUALIFICATIONS:

  • 6 - 10+ years of program or project management experience

  • Hands-on experience working on at least one end-to-end SaMD program (from development through regulatory submission/clearance)

  • Familiarity with: FDA regulatory pathways (e.g., 510(k), De Novo), Design controls (21 CFR 820, ISO 13485) and SaMD development lifecycle

  • Experience working within or closely with Quality Management Systems (QMS)

  • Understanding of key standards such as: IEC 62304 & ISO 14971

  • Proven ability to coordinate across Product, Engineering, Clinical, and Regulatory teams

  • Strong organizational, communication, and stakeholder management skills

  • Experience in wearables, digital health, or consumer health products

  • Experience supporting clinical evidence generation or studies

  • Experience working across multiple concurrent programs

  • Background in a technical or scientific field

This role is based in the WHOOP office located in Boston, MA. The successful candidate must be prepared to relocate if necessary to work out of the Boston, MA office.

Interested in the role, but don’t meet every qualification? We encourage you to still apply! At WHOOP, we believe there is much more to a candidate than what is written on paper, and we value character as much as experience. As we continue to build a diverse and inclusive environment, we encourage anyone who is interested in this role to apply.

WHOOP is an Equal Opportunity Employer and participates in E-verify to determine employment eligibility

The WHOOP compensation philosophy is designed to attract, motivate, and retain exceptional talent by offering competitive base salaries, meaningful equity, and consistent pay practices that reflect our mission and core values.

At WHOOP, we view total compensation as the combination of base salary, equity, and benefits, with equity serving as a key differentiator that aligns our employees with the long-term success of the company and allows every member of our corporate team to own part of WHOOP and share in the company’s long-term growth and success.

The U.S. base salary range for this full-time position is $155,000 - $185,000. Salary ranges are determined by role, level, and location. Within each range, individual pay is based on factors such as job-related skills, experience, performance, and relevant education or training. 

In addition to the base salary, the successful candidate will also receive benefits and a generous equity package.

These ranges may be modified in the future to reflect evolving market conditions and organizational needs. While most offers will typically fall toward the starting point of the range, total compensation will depend on the candidate’s specific qualifications, expertise, and alignment with the role’s requirements.

Skills Required

  • 6–10+ years of program or project management experience
  • Hands-on experience with at least one end-to-end Software as a Medical Device program, from development through regulatory submission or clearance
  • Familiarity with FDA regulatory pathways, including 510(k) and De Novo
  • Knowledge of design controls, 21 CFR 820, and ISO 13485
  • Experience working within or closely with Quality Management Systems
  • Understanding of IEC 62304 and ISO 14971
  • Ability to coordinate across Product, Engineering, Clinical, and Regulatory teams
  • Strong organizational, communication, and stakeholder management skills
  • Experience in wearables, digital health, or consumer health products
  • Experience supporting clinical evidence generation or clinical studies
  • Experience working across multiple concurrent programs
  • Background in a technical or scientific field
  • Preparedness to relocate or work from the WHOOP office in Boston, Massachusetts

What the Team is Saying

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Manan Dedhia
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WHOOP Compensation & Benefits Highlights

  • Parental & Family Support Paid parental leave is listed at 18 weeks with an additional 2‑week transition period, signaling strong support for new parents. This depth stands out relative to typical packages highlighted in the materials.
  • Wellbeing & Lifestyle Benefits Medical, dental, and vision coverage are paired with a $500 annual wellness stipend, a free WHOOP membership plus one to gift, daily meals at the Boston HQ, and access to a gym and recovery tools. These health‑aligned perks reinforce a recovery‑first total rewards philosophy.
  • Equity Value & Accessibility Roles are described as eligible for stock options alongside salary, indicating accessible ownership as part of total rewards. This equity component is consistently highlighted in company materials and third‑party summaries.

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The Company
HQ: Boston, MA
500 Employees
Year Founded: 2012

What We Do

At WHOOP, we’re on a mission to unlock human performance. WHOOP empowers members to perform at a higher level through a deeper understanding of their bodies and daily lives. Our wearable device and performance optimization platform has been adopted by many of the world's greatest athletes and consumers alike.

Why Work With Us

At WHOOP, we’re focused on building an inclusive and equitable team with a strong sense of belonging for everyone—increasing representation in every way as our team grows. We believe that our differences are our source of strength—so much so it’s one of our core values.


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WHOOP Offices

Hybrid Workspace

Employees engage in a combination of remote and on-site work.

Typical time on-site: 4 days a week
HQBoston, MA
Limerick, Limerick, V94 4D83 Ireland
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