5-8 years project managementTechnical background in regulated environmentAgile methodologiesJiraSmartsheet / MS Office / VisioProject scheduling & critical pathCross-functional team leadershipMedical device design controlSoftware development lifecycleBachelor's degree in technical disciplineStrong communication skillsMedical device industry experience
Job Description
Dexcom is seeking a Senior Technical Project Manager for their Data Platform team to manage end-to-end program management activities for complex software projects in a regulated medical device environment. The role involves managing frequent releases, coordinating cross-functional teams, ensuring regulatory compliance, and driving projects from concept through commercialization. The position offers a remote work arrangement with 5-15% travel required.
Overview
Dexcom Corporation (NASDAQ DXCM) is a pioneer and global leader in continuous glucose monitoring (CGM). Founded in 1999, Dexcom has focused on better outcomes for patients, caregivers, and clinicians by delivering solutions for people with diabetes. The company is broadening its vision beyond diabetes to empower people to take control of health through personalized, actionable insights.
The Team
As a member of the Technical Program Management team for Dexcom's Data Platform, you will be part of a fast-paced environment helping deliver programs with new and exciting features aimed at empowering people to take control of their health. This role involves managing frequent releases for multiple data platform components while working with a passionate cross-functional team within a highly regulated environment.
Responsibilities
•Manage and drive end-to-end program management activities for complex software projects from concept to regulatory filing and commercialization
•Develop, track, and report on project plans, detailed project schedules, critical path analysis, project and product risks, change control requests, and project deliverables to management and cross-functional teams
•Lead project and status meetings with internal cross-functional teams, executives, and external partners with confidence and clear communication
•Coordinate activities, tasks, and resources across all departments including software development and testing teams, Quality, Regulatory Affairs, and Operations
•Provide guidance to cross-functional groups on priorities and schedules
•Ensure compliance with internal medical device design control and product development processes as well as regulatory requirements for all aspects of the program
•Positively motivate teams to ensure successful project completion
Requirements
•Strong technical background and experience in project management, ideally in a regulated environment
•Experience in the medical device industry is a plus
•Excellent project management skills including ability to develop and manage detailed schedules, dependencies, priorities, and strict deadlines across multiple simultaneous projects
•Excellent communication skills with the ability to convey information clearly through informal and formal documents and collaborate with cross-functional stakeholders
•Experience with Agile development methodologies and practices as well as the product development process
•Knowledge and experience working with software development tools such as Jira for bug/issue tracking and project management
•Proficiency in Microsoft Office, Smartsheet, and Visio/Lucid Chart
•Strong initiative, self-driven to deliver results without daily supervision
•Highly collaborative with strong organizational, team building, and team leadership skills
•Ability to manage conflict professionally with a strong can-do attitude
Education and Experience
•Bachelor's degree in a technical discipline with 5-8 years of related experience, or
•Master's degree with 2-5 years of equivalent industry experience, or
•PhD with 0-2 years of experience
Compensation and Benefits
•Salary range: $105,800 - $176,300
•Full and comprehensive benefits program
•Growth opportunities on a global scale
•Access to career development through in-house learning programs and/or qualified tuition reimbursement
Work Location
This is a remote position. You are not required to live within commuting distance of a Dexcom site. If you reside within commuting distance of a Dexcom site (typically 75 miles/120km), a hybrid working environment may be available.
Travel Required: 5-15%
Resume Intelligence
Assess your experience against this job and tailor your bullet points instantly.
Sign in required
Please sign in to assess your resume alignment and generate custom copyable work bullets.