Senior Equipment Engineer – Smart Manufacturing & IoT

Dexcom Inc.

Kuala Lumpur

On-site

MYR 120,000 - 180,000

Full time

7 days ago
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Job summary

Dexcom Malaysia is seeking a Senior Equipment Engineer in Penang to maintain and optimize automated manufacturing equipment, lead troubleshooting, support qualification of new systems, and drive continuous improvement.

The role requires a Bachelor's in relevant engineering and 3–5 years in medical device/manufacturing, hands-on with automation, PLC programming, IoT, and SCADA (Ignition). Exposure to GMP/ISO13485 and FDA is preferred. Occasional travel may be required.

Qualifications

  • Bachelor’s degree in Mechanical, Electrical or Mechatronics or related field.
  • 3–5 years in equipment engineering within medical device/manufacturing.
  • Hands-on with automated equipment, preventive maintenance and troubleshooting.

Responsibilities

  • Maintain and optimize automated manufacturing equipment for peak performance.
  • Lead troubleshooting and root cause analysis to minimize downtime.
  • Support installation, setup and qualification of new equipment.
  • Perform on-site equipment buyoff and vendor acceptance testing.
  • Draft IQ/OQ protocols and ensure regulatory compliance.
  • Collaborate on automation, IoT, SCADA and continuous improvement projects.

Skills

Automation systems
Robotics
PLC programming
Pneumatic systems
Electrical troubleshooting
IoT integration
SCADA Ignition
GMP/ISO13485/FDA knowledge
Lean/Six Sigma
TPM

Education

Bachelor's degree in Mechanical, Electrical or Mechatronics

Tools

Siemens PLC
Allen-Bradley PLC
Ignition SCADA

Job description

Dexcom Malaysia is seeking a Senior Equipment Engineer in Penang to maintain and optimize automated manufacturing equipment, lead troubleshooting, support qualification of new systems, and drive continuous improvement.

The role requires a Bachelor's in relevant engineering and 3–5 years in medical device/manufacturing, hands-on with automation, PLC programming, IoT, and SCADA (Ignition). Exposure to GMP/ISO13485 and FDA is preferred. Occasional travel may be required.

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