QC inspector

Hochuen Medical Sdn Bhd; Johor; On-site; MYR 42,000 - 66,000; Full time

Job summary

Hochuen Medical Sdn Bhd is seeking a QC Inspector to inspect, measure and test parts to ensure they meet quality standards and customer requirements. This position belongs to the Quality Department.

You will conduct IQC/FAI/IPQC/OQC inspections of incoming materials, in-process and finished goods, maintain accurate records for ISO audits, operate QC equipment and support root-cause investigations. Qualifications include SPM or equivalent, at least 1 year in quality control in medical device or

Qualifications

• Minimum 1 year of experience in quality control/manufacturing.
• Basic knowledge of ISO 13485 and related quality standards.
• Proficiency with measurement tools and QC documentation.
• Good communication skills in English; Mandarin is a plus.

Responsibilities

• Inspect, measure and test incoming material, in-process and finished goods.
• Maintain accurate inspection records for ISO audits.
• Operate QC inspection and testing equipment.
• Collaborate with production to address quality issues and non-conformances.
• Assist in ISO documents, SOPs and training materials; support internal/external audits.

Skills

Documentation

Attention to detail

Analytical thinking

English & Mandarin

Education

SPM or equivalent

Job description

QC inspectors are responsible for inspecting, measuring and test the part/product to ensure it meets quality standards and customer’s requirements.

This position attached to Quality Department

Key responsibilities:

• Conduct IQC/FAI/IPQC/OQC inspection and testing of incoming material, in-process product and finished goods to verify its conformance with product specifications.
• Maintain accurate and detailed records of inspection of production line (incoming material, in-process and finished goods) and testing data for ISO audit purposes.
• Maintain and operate QC inspection and testing equipment.
• Collaborate with production team to solve quality issues, properly handling of non-conforming or suspected products, report the non-conforming or any defects/deviation to quality supervisor.
• Assist in preparation and implementation of ISO document, SIP, SOP, records and training material ,refer to standard &limited sample as needed.
• Assist in preparation of internal and external audit, ensuring all quality checking documents/records are in compliance with ISO13485.
• Support the investigation of customer complaints, helping to identify root cause and implement corrective actions as necessary.

Qualifications:

• SPM or equivalent
• Minimum of 1 year of experience in quality control manufacturing, preferably in medical device, pharmaceutical or biotechnology industries.
• Basic knowledge of quality standards, for example, ISO 13485.
• Proficiency in using quality control tools and measurement devices, such as callipers, height gauge, image measuring instrument.
• Strong documentation skills, attention to details and ability in analysis and problem-solving.
• Able to communicate in English and Mandarin is an added advantage.