QC Inspector

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 2022 revenues of $2.9B, a growth of 18% over 2021. Headquartered in San Diego, California, with additional offices in the Americas, Europe, and Asia Pacific, the company employs over 8,000 people worldwide.

Summary:

As a member of the Receiving Inspection 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.

Essential Duties and Responsibilities:

• Performs inspections, checks testing and sampling procedures for incoming components, materials, subassemblies, and product as conforming to specified requirements in accordance with material specification, drawing and quality assurance standards.
• Performs and coordinates material transfer verification.
• Performs and coordinates first article inspection.
• Prepares, records, and updates receiving inspection report.
• Ensures all paperwork contains accurate and legible information. Any discrepancies are noted on the receiving inspection report.
• Performs transaction related to QA sample or nonconforming materials in a defined system if applicable.
• Applies approval label, release, and move inspection lots to approve locations, or vice versa apply rejection label and quarantine the nonconforming inspection lots once analytical data is evaluated.
• Initiates non-conforming material report.
• Monitors equipment and instrumentation to ensure it is clean and safe to use.
• Uses the Microsoft Suite of product: Word, Excel, Outlooks.
• Adheres all GMP, safety guidelines and company standards at all time.
• Assumes and performs other duties as assigned.
• Assists onboarding new team member in understanding the inspection and work.
• Able to work independently with minimal supervision by Supervisor.

Required Qualifications:

• Typically requires a high school certificate (SPM) / Diploma or related field with minimum 3 years of relevant industry experience and/or training.
• To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed above are representative of the knowledge, skill, and/or ability required.
• Good computer (Microsoft Suite) skills in compiling report and graph using Microsoft Word, Excel, etc.
• Good interpersonal and teamwork skills.
• Must be able to flex schedule to work in different shifts to meet demand.

Preferred Qualifications:

• Receiving inspection and/or QA/QC experience.
• Min 3 years in in the medical device industry or manufacturing industry previous experience.
• Experience using inspection tools (caliper, micrometer, pin gauges)
• Ability to understand drawings and tolerances.

Education Requirements:

• High school certificate (SPM) / Diploma or equivalent.

Travel Required:

• 0 – 25%

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.