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, CA)#LI-JR1
Location:San Francisco
Actual compensation may vary depending on job-related factors including knowledge, skills, experience, and work location.
Estimated Pay Range$158,000.00 - $206,000.00
