Join to apply for the Senior Process Engineer role at Dexcom.
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 and unlock information and insights that drive better health outcomes. We are broadening our vision beyond diabetes to empower people to take control of health through personalized, actionable insights aimed at solving important health challenges.
Responsibilities
Lead and execute Equipment/Process Qualifications including IQ, OQ, PQ and PPQ on the Sensor dipping process.
Drive process development and improvements.
Characterize key process KPIs to enhance performance and reliability.
Responsible for Installation, Commissioning, and Validation of equipment within Sensors Manufacturing.
Ensure core Operations KPIs (Yield, Performance, Availability, etc.) are met/exceeded.
Provide training to Manufacturing Associates and train Technicians and Engineers.
Develop and maintain project timelines, provide updates, and feedback to project leadership.
Implement problem‑solving techniques to identify potential process risks, assess impact, and develop mitigation plans.
Plan and perform Design of Experiments (DOE) and utilize Six Sigma methodologies to characterize, assess capabilities, and determine optimal processing windows.
Perform statistically robust, industry‑standard analysis of data and present findings to technical teams.
Transfer process knowledge to receiving site operations teams and provide technical training.
Perform other duties as assigned.
Qualifications
Understanding of electrochemistry and chemical process characterization.
Experience supporting equipment qualification/validation.
Strong background in process development, statistical analysis and Design of Experiments.
Experience in medical device manufacturing highly desirable.
Adaptability to fast‑moving and changing environments.
Excellent technical problem‑solving and risk‑management skills.
Strong understanding of risk‑management policies and procedures associated with medical device manufacturing.
Detail oriented with ability to multi‑task while maintaining focus on quality and accuracy.
Strong technical leadership and collaborative skills.
Strong interpersonal and communication skills, both verbal and written.
Ability to travel to other supplier or manufacturing sites, if necessary.
Benefits
A front‑row seat to life‑changing CGM technology and our community.
A full and comprehensive benefits program.
Growth opportunities on a global scale.
Access to career development through in‑house learning programs and/or tuition reimbursement.
An innovative, industry‑leading organization committed to employees, customers, and communities.
Travel Required
10%
Experience and Education Requirements
Typically requires a Bachelor's degree in a technical discipline and a minimum of 5–8 years related experience, or a Master's degree and 2–5 years equivalent industry experience, or a PhD and 0–2 years experience.
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