Senior Technical Project Manager

Dexcom • Remote California, CA

1d • $105,800 - $176,300 • Remote

About The Position

As a member of the Technical Program Management team for Dexcom’s Data Platform, you will be part of a fast-paced environment with a front row seat in helping deliver programs with new and exciting features aimed at empowering people to take control of their health. In this role, you will be managing frequent releases for multiple data platform components while working with a passionate cross-functional team within a highly regulated environment.

Requirements

• Strong technical background and experience in project management ideally in a regulated environment.
• Excellent project management skills, including demonstrated ability to develop and manage a project with a detailed schedule, dependencies with other components or projects, establish priorities, work towards strict deadlines and be able to control several projects with various technologies and in various stages of development simultaneously.
• Excellent communication skills with the ability to information clearly and effectively 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 that provide bug/issue tracking and project management functions.
• Proficiency in Microsoft Office, Smartsheet, and Visio/Lucid Chart is required.
• Strong initiative, self-driven to deliver results without daily supervision.
• Highly collaborative and able to work in a team-based environment.
• Strong organizational skills, team building and team leadership skills.
• Ability to manage conflict professionally, strong “can do” attitude.

Nice To Haves

• Experience in the medical device industry is a plus.

Responsibilities

• Managing and driving 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 and tasks as well as resources across all departments including, software development and testing teams, Quality, Regulatory Affairs, and Operations while providing guidance to these groups on priorities and schedules.
• Responsible for compliance to internal medical device design control and product development process as well as regulatory requirements for all aspects of the program.
• Positively motivate teams to ensure successful project completion.

Benefits

• A 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.

What This Job Offers

• Job Type: Full-time
• Career Level: Senior