Receiving QC Inspector II — Precision Quality Assurance

Dexcom Inc.

Seberang Perai

On-site

MYR 39,000 - 67,000

Full time

14 days+

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Job summary

Dexcom Inc. is seeking a Receiving Inspection QC Inspector in Malaysia to support quality control processes for incoming components, materials, and subassemblies. You will perform inspections, record test data, and ensure documentation accuracy in line with GMP and company standards.

The role requires 2+ years in medical device manufacturing, ability to read drawings and tolerances, and proficiency with calipers, micrometers, and gauge tools.

Qualifications

  • High school certificate (SPM) or related field with ≥2 years’ relevant experience.
  • Good interpersonal and teamwork skills.
  • Able to flex schedule to different shifts.
  • Receiving inspection and/or QA/QC experience.
  • Min 2 years in medical device or manufacturing industry.
  • Experience using inspection tools: caliper, micrometer, pin gauges.
  • Ability to understand drawings and tolerances.

Responsibilities

  • Perform inspections, check testing and sampling for incoming components and materials per specs.
  • Prepare, record and update receiving inspection report forms.
  • Ensure paperwork is accurate and legible; note discrepancies.
  • Handle QA samples or nonconforming materials in the system.
  • Apply approval/rejection labels and move/ quarantine inspection lots as needed.
  • Monitor equipment/instrumentation to stay clean and safe.
  • Use Microsoft Word, Excel, Outlook for documentation.
  • Adhere to GMP, safety guidelines and company standards.
  • Perform other duties as assigned.

Skills

Interpersonal skills
Teamwork
QA/QC experience
Inspection experience
Drawings & tolerances
Inspection tools

Education

High school certificate (SPM)

Tools

Caliper
Micrometer
Pin gauges

Job description

Dexcom Inc. is seeking a Receiving Inspection QC Inspector in Malaysia to support quality control processes for incoming components, materials, and subassemblies. You will perform inspections, record test data, and ensure documentation accuracy in line with GMP and company standards.

The role requires 2+ years in medical device manufacturing, ability to read drawings and tolerances, and proficiency with calipers, micrometers, and gauge tools.

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