Dexcom

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QC Inspector 1-M-Th 5p-3:30a (Finance)



About Dexcom

Founded in 1999, Dexcom, Inc. (NASDAQ: DXCM), develops and markets Continuous Glucose Monitoring (CGM) systems for ambulatory use by people with diabetes and by healthcare providers for the treatment of people with diabetes. The company is the leader in transforming diabetes care and management by providing CGM technology to help patients and healthcare professionals better manage diabetes. Since the company's inception, Dexcom has focused on better outcomes for patients, caregivers, and clinicians by delivering solutions that are best in class-while empowering the community to take control of diabetes. Dexcom reported full-year 2020 revenue of $1.9B, a growth of 30% versus 2019. Headquartered in San Diego, California, with additional offices in the U.S., Europe, and Asia Pacific, the company employs over 6,000 people worldwide.

Functional Description: Support Individual Contributor

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.

Essential Duties & Responsibilities:

  • Responsible for scanning, uploading and archiving of Receiving Inspection Reports on a daily basis for the entire department.
  • Responsible for visual and/or dimensional QC inspection and/or testing of incoming quarantined materials, inspection of in-process materials, labeling, and final commercial product.
  • Responsible for quarantine storage of materials and accurate inventory transactions within the MRP system.
  • Responsible for accurately recording inspection results and maintaining good documentation practices.
  • Utilizes basic computer skills to perform computer transactions related to inspection activities.
  • Assumes and performs other duties as assigned

Required Qualifications:

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed above and below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

  • Minimum of six months QC inspection experience, preferably in a GMP regulated medical device manufacturing environment.
  • Understanding of basic visual and dimensional inspection techniques.
  • Ability to follow written procedures and take direction from supervisor and/or other designated personnel in execution of QC inspection assignments.
  • Demonstrates basic computer skills and performs basic computer transactions.
  • Demonstrates good organizational skills and attention to detail.
  • Must have good written and verbal communication skills.
  • Able to work flexible hours; including possible rotating schedules that may include early morning or evening hours, holidays and weekends. Overtime may be required and may be mandatory at times.

Experience and Education Requirements:
  • Typically requires 0-2 years of related experience and a High school diploma/certificate or equivalent.

Travel Required:
  • Up to 25%

Functional/Business Knowledge:
  • Basic understanding of general job aspects and limited understanding of the detailed aspects of the job.
  • Acquires job skills and learns the policies and procedures required to complete routine tasks.

Functional Description

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.

Functional/Business Knowledge

  • Basic understanding of general job aspects and limited understanding of the detailed aspects of the job.
  • Acquires job skills and learns the policies and procedures required to complete routine tasks.

Scope

  • Work at this level requires following standardized, routine methods, under immediate supervision.
  • Assignments are routine in nature and expectation is to follow pre-established guidelines and procedures.
  • Contacts are mostly within own team and immediate supervisor.

Judgement

  • Little responsibility for decisions as to method or selection of work.
  • Receives detailed instructions on routine work and new assignments.
  • Works under close supervision.

Management

  • N/A

Field Sales

  • N/A

Experience and Education

  • Typically requires 0-2 years of related experience and a High school diploma/certificate or equivalent.

Workplace Type

  • The Workplace Type for this role is Assigned Desk. Based on the nature of your role you will have an assigned desk or office located at a Dexcom site and should plan to be onsite approximately 4-5 days per week.

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 talentacquisition@dexcom.com.

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. Dexcom's AAP may be viewed upon request by contacting Talent Acquisition at talentacquisition@dexcom.com.

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