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Quality Engineer 1
2 weeks ago
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.
Where You Come In
As a member of the Quality Engineering team, you will liaison closely with Receiving Inspection, R&D, Supplier Quality and Operations Engineering to ensure open and timely communication of pipeline project deliverables including but not limited to material specifications, drawings, requirements, fixture design and development, Gage Repeatability & Reproducibility Studies, First Article Inspections, inspection procedures, inspection methods, and sampling plans.
What Makes You Successful
- You will provide direct and ongoing support to Receiving Inspection in evaluating inspection methods, process improvements, sampling plans, coordination of first article component and fixture inspections, selection and qualification of inspection equipment.
- You will work closely with Receiving Inspection, Product Release, Project Quality Engineers, and Supplier Quality Engineers to develop and implement inspection methods, sampling plans, and related procedures.
- You will assist in providing input to the design, development, and implementation of fixtures for measuring component parts.
- You will attend assigned design control and phase exit meetings.
- You will assist in creating vision system CMM programs to semi-automatically measure complex molded component parts and sub-assemblies.
- You will conduct measurement capability assessments (i.e. Gage Repeatability and Reproducibility).
- You will assist in designing and developing methods to determine measurement accuracy and precision through testing and analysis.
- You will conduct process, equipment, and measurement method qualifications or validations.
- You will assist in the design and fabrication of mechanical fixtures, tooling, and equipment for component/sub-assembly measurement.
- You will measure task/project percentage completion at critical stages and take appropriate actions as needed to keep tasks/projects on track.
- You will plan, manage and prioritize tasks/projects, tracks progress toward overall goals, and provide periodic updates to management.
Experience And Education Requirements
- Typically requires a bachelor's degree in mechanical engineering, manufacturing engineering, or related field with a minimum of 0-2 years related experience.
- Intermediate or advanced beginner with inspection equipment such as: CMM (Mitutoyo Vision and Touch Probe System, OGP vision System, digital microscopes, and others).
- Intermediate or advanced beginner with engineering software tools for CAD (SolidWorks preferred), engineering analysis, and statistical analysis (e.g. Minitab)
- Intermediate or advanced beginner with basic statistical analysis (normality, standard deviation, variance, and comparison of data groups) including Gage R&R and test method validation.
- Intermediate or advanced beginner with geometric dimensioning and tolerancing and the ability to read mechanical drawings is a plus.
- Proficiency with Microsoft Office Products.
- Previous direct involvement in the medical device industry or a regulated industry.
- Ability to run self-directed projects, maintain timelines, transfer technology, and execute projects in an R&D and GMP manufacturing environment.
- Ability to deal with ambiguity/uncertainty and a willingness to try new/challenging things.
- Strong interpersonal and teamwork skills.
- Demonstrated written and verbal communication skills.
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.
