Supervisor Manufacturing

Dexcom; George Town; On-site; MYR 30,000 - 60,000; Full time

Job summary

An established industry player is seeking a dedicated supervisor to lead their manufacturing team in a controlled environment. This role involves setting production goals, ensuring adherence to quality standards, and fostering a productive work atmosphere. As part of a pioneering company in health technology, you will play a crucial role in improving health outcomes globally. If you are passionate about making a difference in health management and have experience in high volume manufacturing, this is an exciting opportunity to contribute to innovative solutions that change lives. Join a team that values integrity, ambition, and collaboration.

Qualifications

• 2 to 5 years of experience in high volume manufacturing, preferably in medical devices.
• Thorough understanding of cGMPs and their application in process control.

Responsibilities

• Supervise production goals, organize work, and train employees.
• Ensure compliance with quality standards and monitor manufacturing processes.
• Coordinate with teams to analyze product failures and develop solutions.

Skills

High volume manufacturing experience

Process validation

Good Manufacturing Practices (cGMP)

Flexibility in working shifts

Education

Bachelor's degree

Job description

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 we're 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 we've 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. We've already changed millions of lives and we're 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. We'll get there by constantly reinventing unique biosensing-technology experiences. Though we've 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.

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

1. Responsible for executing to production plan and yields within their area of production.
2. Oversees training and complete training records for all manufacturing personnel.
3. Responsible for ensuring that manufacturing team understands and complies with quality standards and requirements as documented.
4. Regularly monitors the accuracy, completeness, and timeliness of manufacturing processes.
5. Supervises the maintenance of personnel records and timecards for staff.
6. Supports the manufacturing lines to solve issues related with manufacturing processes, equipment, materials, etc.
7. Develops schedules and manpower requirements for assigned areas.
8. Acts as liaison between manufacturing, R&D, and engineering to get engineering requests processed correctly and in a timely manner.
9. 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.
10. 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.
11. Other duties as assigned.

Required Qualifications

1. Experience in high volume manufacturing, (medical device preferred) including start-up, scale-up/scale down and in commercial setting.
2. Experience with process transfers, process validation, and health authority inspections.
3. Thorough understanding of current Good Manufacturing Practices (cGMPs) and they apply to process operation and process control.
4. Flexibility in working shifts to meet demand.

Education Requirements

1. 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

1. 0-25%