The role is based in Batu Kawan, Penang and requires a Bachelor’s degree in Microbiology, Biotechnology, Biological Sciences, or a related field. Candidates with certifications such as ISO 13485 Internal Auditor, sterilization standards (ISO 11135/11137), cleanroom monitoring, GMP, or root cause analysis have an added advantage. The position typically requires 3–5 years of relevant experience in microbiology, contamination control, or quality engineering within a regulated environment, with hands-on exposure to environmental monitoring, cleanroom operations, microbiological testing, and validation activities. Strong knowledge of ISO standards, along with technical writing and data analysis skills, is essential.
From a competency perspective, the role demands strong technical microbiology expertise combined with problem-solving and analytical skills. The candidate should be detail-oriented, capable of working independently, and able to communicate effectively while collaborating across functions such as Quality, Manufacturing, and Engineering. A strong commitment to quality, compliance, and regulatory requirements is critical, along with the ability to manage documentation accurately and consistently.
The role involves working in cleanroom and controlled environments, requiring adherence to strict gowning and contamination control standards. It may include physical tasks such as accessing elevated areas for sampling, handling equipment, and supporting environmental monitoring activities. Occasional travel (less than 10%) to external sterilization sites is required, and the candidate must be flexible to work outside standard hours, including evenings or weekends, to support validation activities and project milestones.
Document routine preventive maintenance and unscheduled failures details on system database
Provide inputs to Shift Coordinator or Equipment Engineer to improve PM cycle-time, tool availability, quality/workmanship, reduce media scrap and cost of ownership.
Provide Technical training and certification for junior technician.
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Communicate closely with CM to ensure all consigned parts are available prior loading.
Ensure accurate inventory and WIP. To identify gaps & area of improvement for better inventory management. To conduct quarterly inventory count and validation at CM.
Work with CM and Asia planning team to ensure build plan and commit and accurately scheduled for the week.
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Document routine preventive maintenance and unscheduled failures details on system database
Provide inputs to Shift Coordinator or Equipment Engineer to improve PM cycle-time, tool availability, quality/workmanship, reduce media scrap and cost of ownership.
Provide Technical training and certification for junior technician.
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Create, review, and coordinate Engineering Change Orders implementation with the CM partner and make process improvement recommendations.
Acts as a primary interface with the Teradyne NPI Ops team / Engineering team during the release of a new assemblies or revisions to assemblies already in use.
To work with the CM partner to drive operation improvement.
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Hands-on experience in SoC and/or FPGA RTL design, testbench development, logic verification, timing closure and debugging in accordance with functional safety requirements.
Demonstrate technical ownership of safety related SoC and/or FPGA Soft IP development and verification with proven ability to generate audit ready Functional Safety evidence in compliance with IEC 61508, ISO 26262 or other safety standards.
Working knowledge of any FPGA primitives such as embedded block RAM, DSP blocks, PLL, oscillators, I/O Gearing, configuration/security or power related silicon features is a plus.
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Identify and derive special handling from design spec, such as NDR, source-sync and latency/skew control DRC/LVS and RV debug and convergence, including analysis for waiver request
Low power design; vector-driven layout optimization and leakage/dynamic power control techniques
Provide technical guidance and review for team members in solving complex challenges, with high problem solving skill and critical thinking capability
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Hands-on experience in FPGA RTL design, testbench development, logic verification, timing closure and debugging.
Expert in one or more FPGA primitives such as embedded block RAM, DSP blocks, PLL, oscillators, I/O Gearing, configuration/security or power related silicon features.
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The role is based in Batu Kawan, Penang and requires a Bachelor’s degree in Microbiology, Biotechnology, Biological Sciences, or a related field. Candidates with certifications such as ISO 13485 Internal Auditor, sterilization standards (ISO 11135/11137), cleanroom monitoring, GMP, or root cause analysis have an added advantage. The position typically requires 3–5 years of relevant experience in microbiology, contamination control, or quality engineering within a regulated environment, with hands-on exposure to environmental monitoring, cleanroom operations, microbiological testing, and validation activities. Strong knowledge of ISO standards, along with technical writing and data analysis skills, is essential.
From a competency perspective, the role demands strong technical microbiology expertise combined with problem-solving and analytical skills. The candidate should be detail-oriented, capable of working independently, and able to communicate effectively while collaborating across functions such as Quality, Manufacturing, and Engineering. A strong commitment to quality, compliance, and regulatory requirements is critical, along with the ability to manage documentation accurately and consistently.
The role involves working in cleanroom and controlled environments, requiring adherence to strict gowning and contamination control standards. It may include physical tasks such as accessing elevated areas for sampling, handling equipment, and supporting environmental monitoring activities. Occasional travel (less than 10%) to external sterilization sites is required, and the candidate must be flexible to work outside standard hours, including evenings or weekends, to support validation activities and project milestones.
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· Conduct investigations for quality incidents related to test equipment and support root cause analysis and corrective actions.
· Perform product conversions on test equipment to support various production requirements.
· Monitor key process input variables (KPIVs) using tools such as the KPOV database, OEE tracking, Maintenance Logs, and the Digital Preventive Maintenance system.
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Document routine preventive maintenance and unscheduled failures details on system database
Provide inputs to Shift Coordinator or Equipment Engineer to improve PM cycle-time, tool availability, quality/workmanship, reduce media scrap and cost of ownership.
Provide Technical training and certification for junior technician.
...
Document routine preventive maintenance and unscheduled failures details on system database
Provide inputs to Shift Coordinator or Equipment Engineer to improve PM cycle-time, tool availability, quality/workmanship, reduce media scrap and cost of ownership.
Provide Technical training and certification for junior technician.
...