Staff Technical Program Manager Quality Compliance

The Company

Dexcom Corporation (NASDAQ DXCM) is a pioneer and global leader in continuous glucose monitoring (CGM). Dexcom began as a small company with a big dream: To forever change how diabetes is managed. To unlock information and insights that drive better health outcomes. Here we are 25 years later having pioneered an industry. And were just getting started. We are broadening our vision beyond diabetes to empower people to take control of health. That means personalized actionable insights aimed at solving important health challenges. To continue what weve started: Improving human health.

We are driven by thousands of ambitious passionate people worldwide who are willing to fight like warriors to earn the trust of our customers by listening serving with integrity thinking big and being dependable. Weve already changed millions of lives and were ready to change millions more. Our future ambition is to become a leading consumer health technology company while continuing to develop solutions for serious health conditions. Well get there by constantly reinventing unique biosensing-technology experiences. Though weve come a long way from our small company days our dreams are bigger than ever. The opportunity to improve health on a global scale stands before us.

Meet the team:

Dexcoms Sustaining Product Quality Team within Corporate Quality Compliance is currently seeking a Staff Technical Program Manager to lead cross functional teams to execute sustaining activities for our cutting-edge this role you will align the vision of our executive management and other cross-team stakeholders to help prioritize the work of the sustaining teams to further develop and improve our commercial products as well as help develop evolve or establish the procedures used to do so. Stakeholders include Program & Product Managers Marketing R&D Operations User Experience (UX) Human Factors and Clinical Regulatory Authority and Quality Assurance teams as well as external teams.

The ideal candidate has a strong foundation in Project Management Practices a solid technical understanding of product sustaining activities experience with product commercialization and requirements definition and can work within a regulated environment to lead high visibility programs across multiple sites.

Where you come in:

• Works in cross functional highly complex product sustaining portfolio using a wide range of program management expertise and the ability to leverage resources in a multitude of adjacent departments to resolve complex issues in effective and creative ways.

• Independently identifies risks to the product sustaining portfolio and develops mitigations with senior stakeholders as well as project team using concepts influence and techniques to conduct in-depth evaluation and problem solving.

• Coordinates leads and oversees strategic planning & gap analysis meetings with senior stakeholder groups to develop strategy models and program forecasts.

• Daily engagement with VPs Directors & Managers with the confidence and ability to lead senior stakeholder meetings and initiate action on assigned items.

• Networks and influences key senior stakeholders across the organization and outside own area of expertise.

• Prepares and delivers change management communication content electronically or in briefings to executive and program leaders to develop awareness knowledge and desire for upcoming program changes and events.

• Oversees sub-project lead adherence to program governance and makes recommendations for updates changes or improvements.

• Independently tracks workstream initiatives develops reporting dashboards makes reports and builds executive briefings.

What makes you successful:

• Ability to develop in-depth knowledge and experience leading cross-functional teams with stakeholders at all levels of the organization.

• Broad business and technical acumen and proven experience working effectively in a matrix organization and ability to collaborate effectively across geographies.

• Integrate process people quality and commitment-centric approach to getting work done - strong customer service orientation.

• Ability to work with different cross-functional stakeholders to establish and ensure a reliable and productive working relationship. Strong partnering skills.

• Good written and oral communication skills including capacity to comfortably interface with senior leaders.

• Exceptional skills in assessing summarizing and presenting business or operational priorities and decision-points for effective timely and efficient management/executive decision-making.

• Demonstrated independent successful management of complex projects and programs.

• Fluent user in Microsoft Word Excel PowerPoint Project SharePoint Visio and Teams.

• Requires significant technical leadership experience and an understanding of regulated change control product development process and medical device design control manufacturing transfer.

• Requires significant technical knowledge and an understanding of FDA/ISO regulations working with GMPs and ISO standards.

Preferred:

• PMP Certification

• Lean Six Sigma Certification

• Fluent use in SmartSheets or Microsoft Project

• Worked within a Technical PMO structure

• Regulated Medical device industry experience

Whatyoullget:

• A front row seat tolife changingCGM technology.Learn about our brave #dexcomwarriors community.

• Afull andcomprehensive benefitsprogram.

• Growth opportunities on a global scale.

• Access tocareer development through in-house learning programs and/orqualifiedtuition reimbursement.

• Anexcitingandinnovativeindustry-leading organizationcommitted to our employeescustomers and the communities we serve.

Travel Required:

• 0-5%

Education and Experience:

• Typically requires a Bachelors degree ina technical discipline and a minimum of 8-12 years related experience or Mastersdegree and 5-7 years equivalent industryexperience or a PhD and 2-4 years ofexperience.

Flex Workplace: Your primary location will be a home office. You will not have an assigned workstation and will work with your manager to determine office visit needs. You must live within commuting distance of your assigned Dexcom site (typically 75 miles/120km).

Please note: The information contained herein is not intended to be an all-inclusive list of the duties and responsibilities of the job nor are they intended to be an all-inclusive list of the skills and abilities required to do the job. Management may at its discretion assign or reassign duties and responsibilities to this job at any time. The duties and responsibilities in this job description may be subject to change at any time due to reasonable accommodation or other reasons. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.

An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity age national origin or protected veteran status and will not be discriminated against on the basis of disability. Dexcoms AAP may be viewed upon request by contacting Talent Acquisition at

If you are an individual with a disability and would like to request a reasonable accommodation as part of the employment selection process please contact Dexcom Talent Acquisition at

Meritain an Aetna Company creates and publishes the Machine-Readable Files on behalf of Dexcom. To link to the Machine-Readable Files please click on the URL provided: all Staffing and Recruiting Agencies: Our Careers Site is only for individuals seeking a job at Dexcom. Only authorized staffing and recruiting agencies may use this site or to submit profiles applications or resumes on specific requisitions. Dexcom does not accept unsolicited resumes or applications from agencies. Please do not forward resumes to the Talent Acquisition team Dexcom employees or any other company location. Dexcom is not responsible for any fees related to unsolicited resumes/applications.

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