Supervisor Manufacturing

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**:
Supervise our controlled environment room by setting goals, organizing and assigning work, training and developing employees, and maintaining a productive, engaging work environment in order to meet established production schedules

**Essential Duties and Responsibilities**:

- Responsible for executing to production plan and yields within their area of production.
- Oversees training and complete training records for all manufacturing personnel.
- Responsible for ensuring that manufacturing team understands and complies with quality standards and requirements as documented.
- Regularly monitors the accuracy, completeness, and timeliness of manufacturing processes.
- Supervises the maintenance of personnel records and timecards for staff.
- Supports the manufacturing lines to solve issues related with manufacturing processes, equipment, materials, etc.
- Develops schedules and manpower requirements for assigned areas.
- Acts as liaison between manufacturing, R&D, and engineering to get engineering requests processed correctly and in a timely manner.
- Accountable for assisting with the efficient, safe and cost-effective operation of the department; for advising and making recommendations to the Manufacturing Manager with respect to these activities.
- Coordinates with various groups such as quality and engineering to analyse product failure data and test results in order to determine causes of problems and develop solutions.
- Other duties as assigned.

**Required Qualifications**:

- Experience in high volume manufacturing, (medical device preferred) including start-up, scale-up/scale down and in commercial setting
- Experience with process transfers, process validation, and health authority inspections
- Flexibility in working shifts to meet demand

**Education Requirements**:

- Bachelor's degree (B. A.) from four-year College or university; 2 to 5 years related experience and/or training; or equivalent combination of education and experience.

**Travel Required**:

- 0-25%