About DexcomFounded 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.Meet the team:Supports quality activities and projects to successfully meet department and corporate goals. Key contributor in support and collaboration for the following:Global (primarily Asia Pacific region) distribution and manufacturing licensingAudits and InspectionsQuality Management System Regulation and StandardsAdditional quality responsibilities as assignedWorks closely with Quality, Regulatory, Commercial, Legal, Supply Chain, and Operations to ensure compliance with numerous agencies and requirements. Where you come in:Your work is primarily achieved by individual along with others, or through project teams, utilizing technical or subject-matter expertise to achieve resultsRequires specific expertise in professional / functional area(s)You will emphasizes in-depth technical / subject-matter knowledge, project management and influence skillsYou are expected to communicate laterally and engage others across the organization and have some level of influence on decisionsWhat makes you successful:Your familiarity with (preferred) or ability to learn global manufacturing and distribution licensing laws, rules, and statutes.Your strong project management skillsYour internal and external audit and inspection activities as assigned (fulfill audit requests, review records for accuracy, scribe, etc.)Your strong communication skills.Your experience in a regulated environment, preferably within medical device, pharma, aerospace, or similar industry.What you'll 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 in-house learning programs and/or qualified tuition reimbursement.An exciting and innovative, industry-leading organization committed to our employees, customers, and the communities we serve.#LI-HybridTo 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 unsolicitedresumes/applications.
