Supervisor Quality Assurance

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:

Our Receiving Inspection teams strive towards managing high volume day to day challenges to ensure our materials meet requirements and ultimately fulfill Customer needs. By joining our team this role ensures we meet internal and external standards and cGMP regulations in our fastpaced work environment.

Where you come in:

• You are responsible for performing a variety of work functions related to inspecting and testing of raw materials component piece parts and finished goods receiving/shipping fulfilment.

• You will develop related inspection procedures train and supervise an inspection team schedule inspection activities ensure proper documentation of inspection results and review inspection documentation for accuracy and conformance to requirements.

• You must be proficient with optical inspection of mechanical parts and workmanship inspection of raw materials. Support supplier quality systems internal audits and assist with investigations of nonconforming material as necessary.

• Performs supervisory and administrative duties associated with inspection personnel management.

• Coordinates the tasks and work plans of the receiving inspection area.

• Observes and verifies the accuracy and adequacy of the inspection activities and records.

• Responsible for material flow storage of parts and accurate inventory transactions physically and within the ERP system.

What makes you successful:

• You must be proficient with optical inspection of mechanical parts and workmanship inspection of raw materials. Support supplier quality systems internal audits and assist with investigations of nonconforming material as necessary

• You are systematic highly organized and able to articulate thoughts well. Must be able to supervise personnel and work in a cGMP regulated environment. Requires interfacing with various QC QA Manufacturing Engineering Management personnel.

• Must be able to multitask several shifting priorities while working in a fastpaced manufacturing environment.

• Directly supervises team employees in the Receiving Inspection QC and Finished Goods QC Department. Carries out supervisory responsibilities in accordance with the organizations policies and applicable laws. Responsibilities include interviewing hiring and training employees; planning assigning and directing work; appraising performance; rewarding and disciplining employees; addressing complaints and resolving problems.

• To perform this job successfully an individual must be able to execute each essential duty satisfactorily. The requirements listed below are representative of the knowledge skill and/or ability required.

• Understanding of multiple acceptance sampling plans ANSI/ASQ Z1.4 Z1.9 and C0.

• Able to read and understand specifications and inspection criteria and to apply criteria using appropriate and properly configured inspection tools. Experience reading schematics and mechanical drawings per ANSI/ASME Y14.24 Y14.35M is preferred.

• A selfmotivated and meticulous individual able to work in a team with minimal supervision.

• Strong computer skills desired; proficient in use of Microsoft Office and database applications. Oracle and ERP experience preferred.

• Must have strong written and verbal communication skills.

• Preferred a minimum of five years receiving inspection supervisory experience or combine supervisory experience preferably in a cGMP regulated medical device manufacturing environment.

• Understanding of geometric tolerancing per ANSI/ASME Y14.5M. Experience with the inspection of electronic assemblies per IPCA610D is preferred.

• Preferred to have the ability to calculate figures and amounts such as proportions percentages area circumference and volume. Ability to apply concepts of basic algebra geometry and trigonometry. Statistical Analysis experience also preferred.

• Optional experience or certified in SolidWorks Statistical Software (JMP or Minitab).

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.

Experience and Education Requirements:

• Typically requires a Bachelors degree with 5 8 years of industry experience.

• Informal management/ team lead expereince

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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