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 uniquebiosensing-technologyexperiences. 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.
A great opportunitywith aface pacedand steadily growing organization; that is new enough to be exciting and full of opportunity and mature enough to have resources and infrastructure. The opportunity to transform the lives of diabetics is exceptionally rewarding.
- You work asaQAengineerof theProduct DevelopmentTeam within the R&D Department, andassistwith defining design inputs, designing components and processes, verifying that design outputs satisfy design inputs, and validating user needs are met.
You work asaQAengineerof theProduct DevelopmentTeam within the R&D Department, andassistwith defining design inputs, designing components and processes, verifying that design outputs satisfy design inputs, and validating user needs are met.
- You Develop processes and perform quality functions that help the company achieve its quality policy requirements andcomply withregulations, including supporting Corrective Action Preventive Actions (CAPAs), Post Market Surveillance, Biocompatibility, Sterilization, Electrical Safety
You Develop processes and perform quality functions that help the company achieve its quality policy requirements andcomply withregulations, including supporting Corrective Action Preventive Actions (CAPAs), Post Market Surveillance, Biocompatibility, Sterilization, Electrical Safety
- You perform analysis of reports and data toidentifytrends, andrecommend updates or changes to quality standards and procedures when necessary.
You perform analysis of reports and data toidentifytrends, andrecommend updates or changes to quality standards and procedures when necessary.
- You ensure compliancetoexternal specifications and standards.
You ensure compliancetoexternal specifications and standards.
- Develop company policies and procedures that help Dexcom achieve its quality policy and compliance with domestic and international regulations.
Develop company policies and procedures that help Dexcom achieve its quality policy and compliance with domestic and international regulations.
- Execute risk management, validation, sample size, and external standards review and implementation activities.
Execute risk management, validation, sample size, and external standards review and implementation activities.
- Develop systems and processes that improve product safety, improve process efficiency, increase product consistency and conformance to requirements, and reducewaste inprocesses
Develop systems and processes that improve product safety, improve process efficiency, increase product consistency and conformance to requirements, and reducewaste inprocesses
- You have knowledge in medical device design control – especially planning, inputs, verification, validation, change, risk management, but alsobiocompatibility/sterilization,electrical safety
You have knowledge in medical device design control – especially planning, inputs, verification, validation, change, risk management, but alsobiocompatibility/sterilization,electrical safety
- Youare able toeffectively adapt to new responsibilities, changes in projects, processes, and industry
Youare able toeffectively adapt to new responsibilities, changes in projects, processes, and industry
- Your experience writing in the medical device or related industry will be extremely valuable todemonstratecompliance to CFR, EUMRD, ISO 13485 and related standards, regulations, and guidance.
Your experience writing in the medical device or related industry will be extremely valuable todemonstratecompliance to CFR, EUMRD, ISO 13485 and related standards, regulations, and guidance.
- Your collaboration and influence through verbal and written means will be an asset
Your collaboration and influence through verbal and written means will be an asset
- Your ability to analyze data through statistical means
Your ability to analyze data through statistical means
- Your analysis and interpretation technical procedures, internationalstandardsand government regulations, to assure safety, high performing products, and compliance
Your analysis and interpretation technical procedures, internationalstandardsand government regulations, to assure safety, high performing products, and compliance
- A front row seat to life changing CGM technology.Learn about our brave #dexcomwarriors community.
A front row seat to life changing CGM technology. .
- A full and comprehensive benefits program.
A full and comprehensive benefits program.
- Growth opportunities on a global scale.
Growth opportunities on a global scale.
- Access to career development through in-house learning programs and/or qualified tuition reimbursement.
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.
An exciting and innovative, industry-leading organization committed to our employees, customers, and the communities we serve.
- Typically requires aBachelorsdegree in a technical discipline, and a minimum of 5-8 years related experience orMastersdegree and 2-5 years equivalent industry experience or a PhD and 0-2years experience.
Typically requires aBachelorsdegree in a technical discipline, and a minimum of 5-8 years related experience orMastersdegree and 2-5 years equivalent industry experience or a PhD and 0-2years 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.
talentacquisition@dexcom.com.
talentacquisition@dexcom.com.
View the OFCCP's Pay Transparency Non Discrimination Provision at this link .
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
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