Receiving Technician - S4
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Before you apply
LocationPenang, Malaysia | N/A
Work modeon-site
Typefull-time
SeniorityMid
Experience4+ yrs
DepartmentSupply Chain
Company size10,000+ people
First seenOct 18, 2026 · 2w ago
Verified live3d ago
At a glanceSummarised by Seekless from the posting.
Diploma in Engineering, Science, Biomedical, Quality, or a related field
Minimum 4 years of experience in Incoming Quality Control (IQC), Receiving Inspection, or a manufacturing/medical device environment
Proficient in using inspection and measurement equipment such as Smartscope, Instron, calipers, micrometers, gauges, and other precision measuring instruments
Strong understanding of Incoming Quality Control (IQC) processes
Knowledge of GMP, ISO 13485, FDA 21 CFR Part 820, Good Documentation Practices (GDP), CAPA, Non-Conformance processes, Sampling Plans, and AQL methodologies
Strong problem-solving and root cause analysis skills
Able to work independently with minimal supervision
Good communication, documentation, and report-writing skills
Experience in the medical device manufacturing industry is highly preferred
Skills
Smartscope
Instron
calipers
micrometers
gauges
Purpose Statement
The Receiving Technician is responsible for providing an independent and unbiased evaluation of incoming materials to ensure they meet quality specifications and regulatory requirements before being released for production. This role supports supplier quality by conducting inspections, managing non-conforming materials, maintaining quality documentation, and contributing to continuous quality improvement.
Minimum Requirements
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Diploma in Engineering, Science, Biomedical, Quality, or a related field.
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Minimum 4 years of experience in Incoming Quality Control (IQC), Receiving Inspection, or a manufacturing/medical device environment.
Key Responsibilities
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Perform incoming inspection of raw materials, components, and purchased parts using approved inspection methods and measuring equipment.
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Verify inspection results and ensure materials comply with drawings, specifications, and quality standards.
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Identify, document, and investigate non-conforming materials, and support root cause analysis and CAPA activities.
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Maintain accurate inspection records and QA documentation in accordance with company procedures.
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Support supplier quality activities, audits, material qualifications, and continuous improvement initiatives.
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Handle discrepant materials according to established procedures and maintain quarantine/MRB inventory when required.
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Ensure compliance with GMP, ISO 13485, FDA Quality System Regulations, and Good Documentation Practices (GDP).
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Provide technical support and guidance on incoming inspection processes as required.
Required Skills & Knowledge
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Proficient in using inspection and measurement equipment such as Smartscope, Instron, calipers, micrometers, gauges, and other precision measuring instruments.
•
Strong understanding of Incoming Quality Control (IQC) processes.
•
Knowledge of GMP, ISO 13485, FDA 21 CFR Part 820, Good Documentation Practices (GDP), CAPA, Non-Conformance processes, Sampling Plans, and AQL methodologies.
•
Strong problem-solving and root cause analysis skills.
•
Able to work independently with minimal supervision.
•
Good communication, documentation, and report-writing skills.
•
Experience in the medical device manufacturing industry is highly preferred.
About the company
About Us
As a global medical technology leader for more than 45 years, our mission at Boston Scientific (NYSE: BSX) is to transform lives through innovative medical solutions that improve the health of patients. If you’re looking to truly make a difference to people both around the world and around the corner, there’s no better place to make it happen.