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Quality Assurance Inspector

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Onsite

Quality Assurance Inspector

Titanium Systems Sdn Bhd

Quality Assurance Inspector

Skills

Testing & QACompliance

2 months ago

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Important information


Contract type:

Permanent

Location:

Johor Bahru, Johor, Malaysia

Work mode:

Onsite

Published on:

24 August 2026

What they need


Position Summary

We are looking for a skilled Quality Assurance Inspector to join our team to support product inspections and ensure our products meet the highest standards of quality and compliance. The QA Inspector will play a critical role in ensuring that products manufactured in our ISO-13485 compliant facility meet all quality standards and regulatory requirements. The role involves performing incoming quality assurance inspections of sub-assemblies, documenting inspection results, and ensuring that all products conform to established standards. The Quality Assurance Inspector will work closely with production teams to address quality issues and support continuous improvement initiatives. Candidates should enjoy working in a fast-paced, mission-driven environment, and be prepared to tackle a broad selection of challenges as the company grows.

Responsibilities

● Product Inspections:

● Conduct detailed incoming quality inspections of sub-assemblies to verify conformance to established specifications.

● Complete and maintain detailed inspection records for each batch or lot inspected, including any deviations or non-conformances found during inspections.

● Document inspection results, noting any discrepancies and ensuring they are reported and addressed promptly.

● Initiate non-conformaning material reports (NCMRs) when necessary.

● Ensure that inspection records are accurate, properly filed, and available for review during audits.

● Provide feedback to production and quality teams on potential quality issues and help identify areas for improvement in the manufacturing process.

● Follow all safety protocols and maintain a clean, safe work environment in compliance with company policies and regulatory requirements.

● Ensure proper handling and disposal of non-conforming products and materials according to safety guidelines.

Requirements :

● Minimum of 3 years of experience in a manufacturing environment, preferably within ISO-13485 or medical device industry

● Strong problem-solving and analytical skills

● Effective communication skills, both verbal and written

● Self-awareness, integrity, authenticity, and a growth mindset

Preferred Skills/Experience :

● Familiarity with ISO-13485 Quality Management Systems (QMS).

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