Dexcom
From Dexcom's careers page
Status: listed on the employer's own careers page when we last checked (daily). Confirm on their site before applying.
What makes you successful: You will perform supervisory and administrative duties associated with inspection personnel management.
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.
A Supervisor QC Inspection manages in maintaining high-quality standards by supporting quality control processes, coordinating inspections, and managing documentation, contributing to the overall quality and compliance of products or services within an organization.
As a member of the QA Receiving Inspection team, you play a vital role in ensuring the quality and compliance of incoming materials and components. Your work supports operational efficiency, sustainability, and adherence to regulatory and internal standards.
You will perform supervisory and administrative duties associated with inspection personnel management.
You will provide direct supervision to support individual contributors/matrix reports.
You will coordinate the tasks and work plans of the Receiving Inspection area.
You will observe and verify the accuracy and adequacy of the inspection activities and records.
You will be responsible for material flow, storage of parts, and accurate inventory transactions within the MRP system.
You will generate and maintain quality metrics and reports, as required, and implement appropriate preventive/corrective actions (as needed) to improve quality. Maintains component and supplier performance data and assists with supplier quality management.
You will identify problems and propose solutions that are timely, cost-effective, and meet quality requirements.
You will assist in development of visual and dimensional inspection/test procedures and material specifications.
You will coordinate first article inspections and supplies data to engineering.
You will work with Logistics and Distribution, Supplier Quality and Operations Engineering and other department personnel, as necessary, to support quality and business objectives. Assumes and performs other duties as assigned.
You will plan, manage and prioritize tasks/projects, tracks progress toward overall goals, and provide periodic updates to management.
0-20%
Typically requires a Bachelor’s degree with 5-8 years of Medical Device or Manufacturing industry.
Informal management/ team lead experience.
Proficiency with inspection equipment such as Vision Measuring Machine (VMM), Vision System, and Digital Microscopes are a plus.
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.
Able to work in 12 hours shift pattern
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.
AI in Hiring Notice: We may use AI supported tools to help make our hiring process more efficient, consistent, and accessible for candidates around the world. All hiring decisions are made by people.
At Dexcom, we are committed to providing a fair and inclusive recruitment process, and welcome candidates of all genders and gender identities to apply. If any wording in this description appears unintentionally gendered or exclusionary, please be assured this is not intentional.
Should a reasonable accommodation be necessary to aid a disability, requests should be sent to Dexcom Talent Acquisition at talentacquisition@dexcom.com.
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