QA Inspector 1 (Shift 1A: Days - Sun - Tues every other Wed from 5AM to 5PM )
About The Position
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.
Requirements
- Strong organization skills and attention to detail.
- Past experience working with the following; Agile/PLM, Oracle and/or Camstar software programs.
- Past experience working with Microsoft 365 products (Excel, Outlook, Word, etc).
- Typically requires a minimum of 0-2 years of related experience and High School diploma/certificate or equivalent.
Responsibilities
- Performs inspections, checks testing and sampling procedures for product manufacturing processes.
- Carries out packaging line, manufacturing inspections and sampling and testing of incoming components and raw materials to ensure that company standards are met.
- Monitors critical equipment and instrumentation.
- May draft procedures and assist with validating or troubleshooting testing methods, including assays.
- May apply approval or rejection labels to bulk raw materials once analytical data is evaluated.
- Perform in-process and final product review of documents for accurate format, signatures, dating and Good Documentation Practices (GDP) for commercial and clinical product in a timely matter.
- Maintain compliance with operating procedures and ensure training is completed prior to the operation of a task.
- Ensure all documentation is legible, complete, and correct.
- Inspect labeling for the finished product.
- Understand and review/approve line clearance activities in manufacturing.
- Perform in-process quality audits in manufacturing to assure compliance with manufacturing documentation and good documentation practices.
- Assist with the NCMR process during manufacturing of commercial and clinical products.
- Perform in-process product inspection and testing for commercial and clinical products.
- Familiarize yourself with the manufacturing processes.
- Provide training for new employees.
- Take on new challenges and expanding roles to assist with growing demands within different areas of the Quality Department.
- Assume and perform other duties as assigned.
Benefits
- A full and comprehensive benefits program.
- Access to career development through in-house learning programs and/or qualified tuition reimbursement.
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
High school or GED
