Quality Control (QC)• Assist in implementing quality management procedures and food safety protocols.• Support product inspections, sensory evaluations, and quality testing activities.• Assist in preparing and reviewing quality and regulatory documentation.• Support audit preparations and food safety certification activities.• Collect, organize, and analyze data for quality monitoring and investigations.• Participate in continuous improvement initiatives to enhance quality processes.Research & Development (R&D)• Assist in new product development, formulation, and ingredient evaluation activities.• Support sensory evaluation preparation and basic laboratory testing.• Assist in shelf-life studies and product assessment activities.• Update and maintain R&D documentation and development records.• Document recipes, preparation methods, and product specifications accurately.• Participate in brainstorming sessions and innovation projects.
Develop, implement, and maintain the Project Quality Management System (QMS) to ensure compliance with contractual requirements, company standards, and applicable regulations. •
Establish and manage project quality plans, Inspection & Test Plans (ITP), quality procedures, and inspection frameworks throughout the project lifecycle. •
Lead quality inspections, testing activities, and quality assurance initiatives to ensure construction works comply with approved drawings, specifications, and industry standards. •
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Conduct site inspections and quality verification activities in accordance with approved Inspection & Test Plans (ITP), project specifications, and quality standards.
Coordinate material testing, workmanship inspections, and quality assessments with consultants, laboratories, and project stakeholders.
Verify construction works comply with approved drawings, specifications, method statements, and contractual requirements.
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As a Quality Assurance Engineer in our Kedah-based manufacturing facility, you will be responsible for ensuring that bonded, coated, and sewn industrial gloves consistently meet customer, regulatory, and internal quality standards. The role involves developing and maintaining quality management systems, monitoring production and inspection activities, investigating product and process non-conformances, implementing corrective and preventive actions (CAPA), and driving continuous improvement initiatives. You will work closely with Production, Engineering, and Supply Chain teams to optimize manufacturing performance, analyze quality data and trends, and support internal and external audits. The position also plays a key role in maintaining compliance with ISO 9001 Quality Management System requirements, SMETA ethical and social compliance standards, and all applicable customer, safety, and regulatory requirements while fostering a culture of quality, continuous improvement, and operational excellence.
Perform Incoming (IQC), In-Process (IPQC), Final (FQC), Outgoing (OQA), and reliability inspections in accordance with inspection plans, specifications, and customer requirements.
Conduct visual, dimensional, functional, and workmanship inspections using approved measuring equipment, inspection methods, and applicable IPC standards.
Verify product compliance with engineering drawings, BOM, specifications, customer requirements, and workmanship standards.
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Conduct comprehensive quality inspections and testing of pharmaceutical products and medical devices at various stages of manufacturing to ensure compliance with established quality standards and specifications
Develop, implement and maintain quality assurance protocols, standard operating procedures (SOPs) and documentation systems in accordance with regulatory requirements and industry best practices
Monitor and analyse quality data, test results and manufacturing records to identify trends, variances and potential areas for improvement
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Product and material inspection: Perform incoming, in-process, and final inspections to check that products and materials meet quality standards and specifications.
Testing: Conduct tests on products and materials to identify defects or deviations.
Documentation: Record inspection results, document any issues found, and update relevant forms or reports.
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QA Team Management : Oversee the daily management of the GTR QA team ( IPQA , FQA ), including daily work scheduling, implementation of monthly performance appraisals, and management of all staff attendance; also responsible for building a personnel training system and continuously conducting skills training to improve the team's overall business capabilities.
Production control : Supervise and review the first piece confirmation of each work order, material verification for production line changes, and consistency verification of material receipts to ensure that quality risks in the veneer production process are effectively controlled.
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Perform Incoming Quality Control (IQC), In-Process Quality Control (IPQC), Final Quality Control (FQC), Outgoing Quality Assurance (OQA), and reliability inspections according to inspection plans, specifications, and customer requirements.
Conduct visual, dimensional, functional, and workmanship inspections using approved measuring equipment, inspection methods, and applicable IPC standards.
Verify product compliance with engineering drawings, specifications, Bills of Material (BOM), customer requirements, and workmanship standards.
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Develop and lead key wafer function test hardware solutions, including tester-to-prober interfaces, probe interface boards, probe cards, docking hardware, and test head handling concepts
Translate product, equipment, and manufacturing requirements into robust hardware concepts that support different device technologies, tester platforms, prober models, and production environments
Contribute to the definition, refinement, and standardization of prober docking solutions for broader usage, with focus on repeatability, planarity control, alignment accuracy, maintainability, safety, and ease of setup
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Perform electrical failure analysis, identifying and researching component failures to support Intel factory reject. Your responsibilities will include but not be limited to:
Perform electrical validation and fault isolation using analytical tools such as Parametric Analyzer (I/V analysis), Keithley meter, iTDR, EOTPR, CTMB/ SBTS, micro-probing, SEM/EDX, IRLC etc.
Perform CSAM (C-mode Scanning Acoustic Microscopy) to detect defect.
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Prepare, compile, review and submit product registration and variation applications to the relevant regulatory authorities (e.g., NPRA).
Monitor the status of product registrations, renewals, amendments and variations. Ensure all product registrations are maintained in compliance with current regulatory requirements.
Liaise with regulatory authorities regarding product registration matters and respond to queries promptly. Coordinate with internal departments such as R&D, Quality Assurance, Production, Purchasing, Marketing and Sales to obtain required documentation.
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• Lead test strategy development and Design for Testability (DFT) execution throughout the NPI phase-gate process, including concept review, EVT, DVT, PVT, qualification, and mass production readiness, ensuring on-time deliverables, product quality, manufacturability, and operational excellence
• Collaborate closely with customers, R&D, manufacturing, quality, and operations teams to ensure successful product transfer from development to production.
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R&D Collaboration & Tool Qualification. Partner with R&D teams to support probing and testing tool qualification. Evaluate new test methods, tools, and technologies to ensure readiness for production. Provide technical feedback to improve test coverage, accuracy, and efficiency.
Sustaining & Process Improvement. Work closely with sustaining engineering teams on maintenance strategies and process-related issues. Drive continuous improvement initiatives to enhance yield, quality, and test efficiency. Troubleshoot test-related issues and implement corrective/preventive actions.
Risk Management & Process Control. Conduct risk assessments for test processes and equipment. Develop and maintain Control Plans to ensure process stability. Create and implement OCAP (Out of Control Action Plans). Prepare and maintain detailed Work Instructions for test operations.
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