QA Inspector 2

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 were 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 weve 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. Weve already changed millions of lives and were 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. Well get there by constantly reinventing unique biosensingtechnology experiences. Though weve 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.

Meet the team:

As a member of the QA Lot Release team the inspector is responsible to ensure the activities related to the inspection functions in a manner which meets company standards and methods as determined by quality assurance or other engineering departments.

Performs inspections checks testing and sampling procedures for product manufacturing processes. Carries out packaging line manufacturing inspections and sampling and testing of inprocess and Lot Release to ensure that company standards are met. Monitors critical equipment and instrumentation. May apply approval or rejection labels to lot/product once analytical data is evaluated.

Where you come in:

• Performing inprocess and final product review of documents for accurate format signatures dating and Good Documentation Practices 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 per current Good Manufacturing Practices (GMP).

• Inspect labeling for the finished product.

• Understand and perform line clearance activities in manufacturing.

• Perform inprocess quality audits in manufacturing to assure compliance to manufacturing documentation and good documentation practices.

• Assist with the NCMR process during manufacturing of commercial and clinical product.

• Demonstrate good computer skills and perform computer operations to generate reports and graphs using Microsoft Word and Excel.

• Perform inprocess product inspection and testing for commercial and clinical product.

• Must be able to distinguish between certain colors and pass an annual color vision test.

• Familiarize yourself with the manufacturing processes.

• Review shipping documentation to assure accurate order shipment.

• Works closely with Research & Development Engineering and Manufacturing groups.

• Provide training for new employees.

• Takes on new challenges and expanding roles to assist with growing demands within different areas of the Quality Department.

• Must have strong organization skills and attention to detail.

• Coordinate the completion of group training with the department.

• Identifies problems and proposed solutions that are timely costeffective and meet quality requirements.

• Assist the Supervisor with updates on the department changes and scheduling conflicts.

• Must be able to have the knowledge to make decisions concerning quality questions and objective.

• Work schedule: First shift.

What makes you successful:

• Works closely with Research & Development Engineering and Manufacturing groups.

• Takes on new challenges and expanding roles to assist with growing demands within different areas of the Quality Department.

• Must have strong organization skills and attention to detail

• Identifies problems and proposed solutions that are timely costeffective and meet quality requirements.

• Must be able to have the knowledge to make decisions concerning quality questions and objective

What youll get:

• A front row seat to life changing CGM technology. Learn about our brave #dexcomwarriors community.

• A full and comprehensive benefits program.

• Growth opportunities on a global scale.

• Access to career development through inhouse learning programs and/or qualified tuition reimbursement.

• An exciting and innovative industryleading organization committed to our employees customers and the communities we serve.

Travel Required:

• 05

Experience and Education Requirements:

• Typically requires a minimum 24 years of related experience and a High School diploma/certificate or equivalent

Please note: The information contained herein is not intended to be an allinclusive list of the duties and responsibilities of the job nor are they intended to be an allinclusive 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.

An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity age national origin or protected veteran status and will not be discriminated against on the basis of disability. Dexcoms AAP may be viewed upon request by contacting Talent Acquisition at

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

View the OFCCPs Pay Transparency Non Discrimination Provision at this link.

Meritain an Aetna Company creates and publishes the MachineReadable Files on behalf of Dexcom. To link to the MachineReadable Files please click on the URL provided: 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.

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