Job description

Career-defining. Life-changing. At iRhythm, you’ll have the opportunity to grow your skills and your career while impacting the lives of people around the world. iRhythm is shaping a future where everyone, everywhere can access the best possible cardiac health solutions. Every day, we collaborate, create, and constantly reimagine what’s possible. We think big and move fast, driven by our commitment to put patients first and improve lives. We need builders like you. Curious and innovative problem solvers looking for the chance to meaningfully shape the future of cardiac health, our company, and your career About This Role: iRhythm is currently seeking an experienced Senior Technical Project Manager within the Research & Development team. This Technical Project Manager is focused on embedded hardware and firmware with responsibility for leading the planning, execution, and delivery of complex embedded systems products from concept through production. You will have the opportunity to drive the delivery of medical device projects to domestic and international markets. You will be exposed to a diverse set of projects involving development and testing in the context of addressing unmet clinical needs. In addition, you will build a deep understanding of our end-to-end systems, helping to drive successful delivery of projects throughout the development life cycle. Our work environment is fast-paced, with a collaborative atmosphere. Most of all, we are passionate about delivering innovations that improve the quality of health care and the patient experience. We are looking for like-minded individuals to join our team today! Specific job responsibilities include: Project Planning Collaborate closely with product management, engineering, quality and regulatory assurance to understand and distill business priorities to develop project scope for unmet clinical needs and launch new products Drives project planning, WBS, estimation, resources, scheduling, timelines, “what-ifs”, risks and re-planning as required with focus on embedded hardware and firmware components. Create and maintain the technical project release plan as it pertains to design control process Project Execution Primary owner of project plan initiation through post implementation Successful project execution and launch with a mix of people skills, project management, technical expertise and cross functional collaboration with CRM, Manufacturing, Marketing, Customer Support, and Clinical Operations Ensures all technical project documentation supporting change requests, design change plans, closure forms is executed timely and in compliance with company SOPs/Regulatory standards. Act as a scrum master for sprint planning, backlog refinement, stand-ups, and retrospectives Lead and drive stand-ups, recurring project meetings to track progress, timelines, project health and risks Facilitate and participate in technical discussions within technical engineers and cross-functional teams Own project risk register and hold regular discussions on risk management activities. Work closely with QA/RA to ensure activities performed in compliance with Company SOPs/International Regulatory standards. Operational In conjunction with technical project management team, own health of projects undertaken and drive continuous improvement of processes Drive best practices on the team, deal with ambiguity and competing objectives Participate in production release/health monitoring activities. Required Qualifications: BS degree in Engineering or related technical field required Master’s degree, M.B.A. or P.M.P. certification a strong plus 4 years’ experience leading development projects, ideally with a demonstrated record of transferring design changes to manufacturing and taking new products from development to commercialization. 8 years of engineering experience in a professional environment, requiring extensive cross-functional collaboration. Proven ability to influence without authority, enabling coordination and alignment of matrixed resources. Strong project management skills including budgeting, planning, tracking, organization, attention to detail, managing competing priorities, analytical and critical thinking, and sound engineering fundamentals Strong technical abilities, grounded in ethics and sound decision-making processes. Deep familiarity with highly technical product development teams and design transfer processes with embedded systems - medical device experience is strongly preferred. Excellent interpersonal skills, enabling strong alignment with internal / external partners and can navigate conflict constructively. Effective communication and presentation abilities, with demonstrated ability to synthesize information clearly and convey technical concepts to non-technical audiences. Software/tools: Proficient using Microsoft Office Suite, including Project and Visio. Working knowledge of Atlassian tools (JIRA, confluence) a plus. Travel up to 10% (team meetings/offsites) Preferred Qualifications: Master’s in science or technical field is a plus Experience in the medical device industry is a plus Experience with IEC standards 62304, 14971, 62366 Experience with Tools desired – Jira, Confluence, Requirements management (JAMA) Proficiency in AWS/Linux/Unix/Windows environment Location: Hybrid (San Francisco, or Cypress, CA) #LI-JR1 Location: Orange County Actual compensation may vary depending on job-related factors including knowledge, skills, experience, and work location. Estimated Pay Range $138,000.00 - $180,000.00 As a part of our core values, we ensure an inclusive workforce. We welcome and celebrate people of all backgrounds, experiences, skills, and perspectives. iRhythm Technologies, Inc. is an Equal Opportunity Employer. We will consider for employment all qualified applicants with arrest and conviction records in accordance with all applicable laws. iRhythm provides reasonable accommodations for qualified individuals with disabilities in job application procedures, including those who may have any difficulty using our online system. If you need such an accommodation, you may contact us at taops irhythmtech.com About iRhythm Technologies iRhythm is a leading digital healthcare company that creates trusted solutions that detect, predict, and prevent disease. Combining wearable biosensors and cloud-based data analytics with powerful proprietary algorithms, iRhythm distills data from millions of heartbeats into clinically actionable information. Through a relentless focus on patient care, iRhythm’s vision is to deliver better data, better insights, and better health for all. Make iRhythm your path forward. Zio, the heart monitor that changed the game. There have been instances where individuals not associated with iRhythm have impersonated iRhythm employees pretending to be involved in the iRhythm recruiting process, or created postings for positions that do not exist. Please note that all open positions will always be shown here on the iRhythm Careers page, and all communications regarding the application, interview and hiring process will come from a irhythmtech.com email address. Please check any communications to be sure they come directly from irhythmtech.com email address. If you believe you have been the victim of an imposter or want to confirm that the person you are communicating with is legitimate, please contact taops irhythmtech.com. Written offers of employment will be extended in a formal offer letter from an irhythmtech.com email address ONLY . For more information, see ftc.gov and ic3.gov

Requirements

Must-haves

Career-defining. Life-changing.
Project Planning
Collaborate closely with product management, engineering, quality and regulatory assurance to understand and distill business priorities to develop project scope for unmet clinical needs and launch new products
Drives project planning, WBS, estimation, resources, scheduling, timelines, “what-ifs”, risks and re-planning as required with focus on embedded hardware and firmware components.
Create and maintain the technical project release plan as it pertains to design control process
Project Execution
Primary owner of project plan initiation through post implementation
Ensures all technical project documentation supporting change requests, design change plans, closure forms is executed timely and in compliance with company SOPs/Regulatory standards.
Act as a scrum master for sprint planning, backlog refinement, stand-ups, and retrospectives
Lead and drive stand-ups, recurring project meetings to track progress, timelines, project health and risks
Facilitate and participate in technical discussions within technical engineers and cross-functional teams
Own project risk register and hold regular discussions on risk management activities.
Work closely with QA/RA to ensure activities performed in compliance with Company SOPs/International Regulatory standards.
In conjunction with technical project management team, own health of projects undertaken and drive continuous improvement of processes
Drive best practices on the team, deal with ambiguity and competing objectives
Participate in production release/health monitoring activities.

Nice-to-haves

Deep familiarity with highly technical product development teams and design transfer processes with embedded systems - medical device experience is strongly preferred.
Software/tools: Proficient using Microsoft Office Suite, including Project and Visio. Working knowledge of Atlassian tools (JIRA, confluence) a plus.
Master’s in science or technical field is a plus
Experience in the medical device industry is a plus
Experience with IEC standards 62304, 14971, 62366
Experience with Tools desired – Jira, Confluence, Requirements management (JAMA)
Proficiency in AWS/Linux/Unix/Windows environment
Location: Hybrid (San Francisco, or Cypress, CA)

Application prep

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Keywords to mirror

scrumjiraaws

Platform: workday
Effort: long

Benefits

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