QC Inspector

Jayfen Health (M) Sdn Bhd; Klang City; On-site; MYR 100,000 - 150,000; Full time

Job summary

A leading healthcare manufacturing company in Klang, Selangor, is looking for a QC Inspection to ensure quality and compliance in processes. The role requires performing inspections on materials and products, maintaining records, and identifying nonconformities. Candidates should have 1-3 years of experience in a regulated environment and a high school diploma. Attention to detail and familiarity with industry regulations are essential to succeed in this full-time position.

Qualifications

• High school diploma or equivalent.
• 1–3 years of Quality Control inspection experience in a regulated environment.
• Familiarity with GMP, FDA QSR, and/or ISO 13485.

Responsibilities

• Perform inspections on incoming materials and finished medical devices.
• Document inspection results in batch records and electronic quality systems.
• Ensure compliance with FDA QSR, ISO 13485, and GMP.

Skills

Attention to detail

Inspection techniques

Documentation skills

Basic computer skills

Education

High school diploma or equivalent

Tools

Quality Management Systems (QMS)

Enterprise Resource Planning (ERP)

Job description

Jayfen Health (M) Sdn Bhd, a leading healthcare manufacturing company, is seeking a talented QC Inspection to join our dynamic team in Klang, Selangor. As a full-time role, you will play a pivotal part in ensuring the highest standards of quality and compliance across our manufacturing processes.

Key Responsibilities

• Perform inspections on incoming materials, in-process assemblies, and finished medical devices according to approved procedures
• Inspect products using visual inspection, measuring tools, and test equipment (e.g., calipers, micrometers, gauges, microscopes)
• Verify product conformance to approved specifications and work instructions
• Accurately document inspection results in batch records, inspection reports, and electronic quality systems
• Identify, document, and elevate nonconforming materials in accordance with established NCR procedures
• Support investigations related to defects, deviations, and CAPAs
• Ensure inspection activities comply with FDA QSR (21 CFR Part 820), ISO 13485, and GMP requirements
• Maintain inspection records in accordance with document control and data integrity requirements
• Participate in training, audits, and continuous improvement initiatives

Required Qualifications

• High school diploma or equivalent
• 1–3 years of Quality Control inspection experience in a regulated manufacturing environment
• Prior experience in medical device, pharmaceutical, or other regulated industries preferred
• Familiarity with GMP, FDA QSR, and/or ISO 13485 requirements
• Strong attention to detail and ability to accurately document inspection results
• Basic computer skills, including experience with QMS, ERP, or electronic inspection systems