Dexcom
Senior Process Development Engineer
San Diego, California · Senior
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About the role
- 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.
- That means personalized, actionable insights aimed at solving important health challenges.
Responsibilities
- Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.
- Meritain, an Aetna Company, creates and publishes the Machine-Readable Files on behalf of Dexcom.
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.
- Travel Required:
Compensation
- $91,400.00 - $152,300.00
Benefits
- A full and comprehensive benefits program.
- Access to career development through in-house learning programs and/or qualified tuition reimbursement.
- Experience and Education Requirements:
Company info
- You will participate in new product process development, design of experiments and measurement system analyses to collect and analyze applicable data relative to program process development targets.
- You execute design control activities with emphasis on design transfer and an understanding of system design and the linkage between technical and business requirements, design and process failure modes and process controls.
- You will review design changes and optimize manufacturing processes for new and existing medical devices, focusing on scalability, efficiency, and quality improvements.
- You will utilize statistical tools and methods to analyze process data, conduct capability studies, and implement process controls.
- You will help develop and execute test methods with necessary protocols and reports to validate process performance and product quality.
- You will collaborate cross-functionally with R&D, Quality Assurance, Regulatory Affairs, Supply Chain, Manufacturing to ensure seamless business strategy and transfer of technical deliverables in the quality management system.
- You have a degree in Mechanical Engineering, Biomedical Engineering, Chemical Engineering or related field; Master's degree preferred.
- Your proficiency is an understanding of experimental study design and measurement system analysis, including the appropriate statistical approaches to data analysis.
- You bring an understanding of medical device design transfer with knowledge of quality and regulatory standards.
- You have experience in at least 1 of the following areas; Plastic component assembly, needles, adhesives, epoxies and curing, and packaging (sterile barrier, secondary, tertiary boxing)
- You are able to communicate effectively and generate PowerPoint presentations to deliver objectives and outcomes from the technical team up through executive leadership.
- You bring cross-functional collaboration experience amongst peers and leaders.
- A front row seat to life changing CGM technology. Learn about our brave #dexcomwarriors community.
Equal opportunity
- The duties and responsibilities in this job description may be subject to change at any time due to reasonable accommodation or other reasons.
- An Equal Opportunity Employer.
- 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.
This listing is sourced directly from Dexcom's careers page and normalized into a canonical job model.