Senior Project Manager - Robotics R&D (Remote)

Posted 2 Days Ago
Be an Early Applicant
Hiring Remotely in Enterprise, FL, USA
In-Office or Remote
89K-222K Annually
Senior level
Healthtech
The Role
Leads complex, cross-functional medical device robotics projects from inception through product release. Manages scope, schedules, budgets, resources, milestones, risks, and dependencies while coordinating R&D, Quality, Regulatory, technical, and leadership stakeholders. Drives accountability and project execution without direct authority, communicates progress and decisions, removes barriers, and balances competing priorities. The role requires experience in regulated product development, preferably with new product development and large technical projects.
Summary Generated by Built In
Work Flexibility: Remote

As a Senior Project Manager, you will lead complex, cross-functional projects supporting the development of innovative medical device products within Stryker’s Digital Robotics and Enabling Technologies business. You will partner closely with R&D, Quality, Regulatory, and other stakeholders to drive programs from inception through product release.


In this highly collaborative role, you will be responsible for aligning teams around project objectives, driving accountability without direct authority, and balancing scope, schedule, resources, budget, and risk to deliver successful outcomes.


This is a remote position, with a preference for candidates residing in the Eastern or Central time zones.


To learn about Stryker's Robotics portfolio, please click here - Mako SmartRobotics Overview | Stryker.


What You Will Do

  • Lead cross-functional project teams through the product development lifecycle, driving alignment, accountability, and execution from inception through product release.
  • Develop and manage project scope, schedules, budgets, resources, milestones, and deliverables to achieve program objectives.
  • Partner with R&D, Quality, Regulatory, and other cross-functional stakeholders to identify dependencies, remove barriers, and maintain project momentum.
  • Influence and motivate cross-functional teams without direct authority, establishing clear ownership and accountability for project commitments.
  • Proactively identify, assess, and manage project risks, developing mitigation strategies to minimize impact to program objectives.
  • Serve as a key source of project information, providing clear and timely updates on progress, risks, decisions, and priorities.
  • Build strong stakeholder relationships and tailor communication effectively across technical teams and organizational leadership.
  • Maintain strong attention to detail while balancing competing priorities and broader program objectives.
  • Partner with technical leaders to understand complex technical challenges and their impact on overall project scope, schedule, resources, and risk.

What You Need


Required Qualifications

  • Bachelor’s degree in Engineering, Computer Science, Biomedical Engineering, or a related technical discipline.
  • Minimum 6 years of relevant experience, including demonstrated project or program management leadership experience.
  • Experience working within the medical device industry or a similarly regulated product-development environment.
  • Proven ability to influence, lead, and drive accountability across teams without direct reporting authority.
  • Strong communication and stakeholder-management skills with the ability to effectively communicate across technical and leadership audiences.
  • Experience managing project scope, schedule, resources, budget, risk, and competing priorities.

Preferred Qualifications

  • PMP certification or equivalent formal project management training.
  • Experience supporting new product development from concept through product release.
  • Demonstrated experience leading large complex, cross-functional product development projects involving technical and business stakeholders.
  • Systems engineering, biomedical engineering, or similar technical background.

  


United States of America Pay Ranges:

  • Puerto Rico: $89,300 - $148,800 USD Annual
  • USN: $102,600 - $171,000 USD Annual
  • US5: $107,700 - $179,600 USD Annual
  • US10: $112,900 - $188,100 USD Annual
  • US15: $118,000 - $196,600 USD Annual
  • US20: $123,100 - $205,200 USD Annual
  • US30: $133,400 - $222,300 USD Annual
View the U.S. work location and transparency guide to find the pay range for your location.

  


Travel Percentage: 20%

Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer – M/F/Veteran/Disability.

Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information.

Skills Required

  • Bachelor's degree in Engineering, Computer Science, Biomedical Engineering, or a related technical discipline
  • Minimum 6 years of relevant experience, including project or program management leadership experience
  • Experience working within the medical device industry or a similarly regulated product-development environment
  • Ability to influence, lead, and drive accountability across teams without direct reporting authority
  • Strong communication and stakeholder-management skills across technical and leadership audiences
  • Experience managing project scope, schedule, resources, budget, risk, and competing priorities
  • PMP certification or equivalent formal project management training
  • Experience supporting new product development from concept through product release
  • Experience leading large, complex, cross-functional product development projects involving technical and business stakeholders
  • Systems engineering, biomedical engineering, or similar technical background

Inari Medical Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Inari Medical and has not been reviewed or approved by Inari Medical.

  • Fair & Transparent Compensation — Pay is considered competitive for many roles, with employees described as 'extremely happy' with total compensation including pay, stock, equity, and benefits. Feedback suggests above‑average salary levels across departments contribute to strong pay sentiment.
  • Healthcare Strength — Benefits include comprehensive medical, dental, and vision coverage, with 100% employer‑paid premiums for employees cited in multiple descriptions. Additional options like critical illness, accident, hospital indemnity, and wellness programs reinforce the healthcare offering.
  • Leave & Time Off Breadth — Time off is characterized by unlimited PTO, cited as a top benefit by employees. Paid holidays and flexible hours are also referenced, expanding the range of time‑off options.

Inari Medical Insights

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The Company
HQ: Irvine, CA
956 Employees

What We Do

Inari Medical, Inc. is a commercial-stage medical device company focused on developing products to treat and transform the lives of patients suffering from venous diseases.

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