Quality Control Assistant

2 days ago

Johor Bahru, Johor, Malaysia ResMed (Malaysia) Sdn Bhd (MY) Full time $36,000 - $72,000 per year

About the Role

The primary role of the Manufacturing Quality function is to design, implement, and monitor quality control programs. Key responsibilities include recommending improvements to methods, procedures, and standards based on data analysis, ensuring products are built correctly to specification, meeting quality standards, and complying with applicable regulatory requirements. This role also involves identifying, reporting, and tracking product defects until resolution.

Responsibilities

The primary objective of the Quality Control specialization within the Manufacturing Quality Job Family is to perform inspections, testing, and sampling activities throughout the product manufacturing process.

Key Responsibilities Include:

Inspection & Testing

  • Perform manufacturing line inspections, sampling, and testing of incoming components, raw materials, in-process items, and finished products to ensure compliance with company and regulatory standards.
  • Conduct visual, dimensional, and functional checks based on established procedures and specifications.
  • Apply approval or rejection labels to raw materials, in-process goods, and finished products accordingly.

Documentation & Procedure Compliance

  • Record inspection results accurately and maintain proper documentation in accordance with QMS, ISO 13485, and GMP requirements.
  • Assist in drafting inspection procedures and support validation or troubleshooting of testing methods when required.
  • Handle non-conforming materials by proper segregation, documentation, and follow-up actions.

Product Release & Non-Conformance Management

  • Support the release of conforming finished goods.
  • Participate in the handling, investigation, and tracking of non-conforming products.

Operational & Support Tasks

  • Perform clerical, administrative, specialized support, or operational tasks as required within the manufacturing or QC environment.
  • Follow established SOPs closely, with limited discretion to deviate from procedures.
  • Interact internally with production, engineering, and other departments to exchange essential quality information.

Qualifications & Experience

Required:

  • SPM holder or equivalent.
  • Minimum 1 year of related experience in quality control, manufacturing, or inspection tasks (preferably in medical device, electronics, or regulated industries).
  • Broad knowledge of daily QC routines and processes to handle standard work situations.
  • Ability to follow instructions and work independently after training, with guidance needed only for new assignments.


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