Sr Medical Device Engineer (Process Development, Sensor Focus)

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 we're 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 we've 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. We've already changed millions of lives and we're 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. We'll get there by constantly reinventing unique biosensing-technology experiences. Though we've 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:

Welcome to our dynamic team, where we pioneer the development of processes and equipment for all iterations of Dexcom wearables and applicators. From cutting-edge research concepts to the efficient production machinery responsible for crafting millions of sensors annually, our team plays a pivotal role in shaping the future of Dexcom technology. Join us in this exceptional and thrilling work environment within a stellar company, where your technical prowess and creative contributions directly influence the lives of our customers daily, both now and in the days to come.

Where you come in:

• You will design and integrate equipment and processes to manufacture R&D scale builds that will eventually scale into commercial processes
• You will develop processes and evaluation systems to support DOEs for R&D Projects.
• You will develop and maintain project timelines and provide updates and feedback to project leadership.
• You lead material characterization, dispensing, and cure-related projects, including root-cause analysis, material qualification, and second sourcing.
• You design and develop fixtures and equipment components required to meet process goals from concept to implementation.
• You will design, document, and optimize new manufacturing processes, assembly steps, and operating procedures for new stations, equipment, and processes within a regulated quality system.
• You demonstrate hands-on process understanding and provide guidance and training to pilot plant operators on engineering-level builds.
• You create and release equipment specifications and drawings, establish calibration, and preventative maintenance requirements.
• You will set up infrastructure for data to be acquired in you measurement and fabrication processes and you will process large data sets to draw conclusions.
• You provide technical oversight and coordinate Research and Development builds within a pilot production facility for multiple projects and project teams.
• You implement, characterize, and optimize processes, mechanical tests, and fixtures/jigs for assembly, inspection, and test through the implementation of measurement systems, part inspections, MSA, and capability analysis.
• You identify process risks and track mitigations through standard methods.
• You assist in scaling up equipment and processes from prototype to pilot to full-scale manufacturing, providing design and assembly requirements within the scope determined by business and schedule needs.
• You exercise judgment within defined procedures and policies to determine appropriate action.

What makes you successful:

• You have the ability to run self-directed projects, maintain timelines, transfer technology, and execute projects in an R&D environment.
• You can deal with ambiguity and uncertainty, and you are willing to try new and challenging things.
• You have experience with operating and programming signal processing equipment &/or automated liquid handling robotics platforms and complex laboratory systems.
• You have proven ability to work hands-on in a fast-paced environment.
• You have previous direct involvement in the medical device industry.
• You are proficient in the use of SolidWorks or equivalent CAD software.
• You are familiar with data analysis methods and analysis software, with experience in JMP preferred.
• You are detail-oriented with strong time management skills.
• You have excellent communication (written and verbal) and personal interaction skills.
• You have knowledge of high reliability, high volume manufacturing processes and designs.

What you’ll get:

• A front row seat to life changing CGM technology. [Learn about our brave #dexcomwarriors community](https://www.dexcom.com/warriors).
• 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.
• An exciting and innovative, industry-leading organization committed to our employees, customers, and the communities we serve.

Travel Required:

• 0-5%

Experience and Education Requirements:

Typically requires a Bachelor’s degree in a technical discipline, and a minimum of 5-8 years related experience or Master’s degree and 2-5 years equivalent industry experience or a PhD and 0-2 years experience.

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. Dexcom’s AAP may be viewed upon request by contacting Talent Acquisition at talentacquisition@dexcom.com.

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 talentacquisition@dexcom.com.

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: [https://health1.meritain.com/app/public/#/one/insurerCode=MERITAIN_I&brandCode=MERITAINOVER/machine-readable-transparency-in-coverage?reportingEntityType=TPA_19874&lock=true](https://protect-us.mimecast.com/s/fufTCyPOPqFWlgBzhMXJ2t?domain=health1.meritain.com)

To 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.