Senior Test Engineer - IVD & Medical Devices, NPI/Validation

Jabil Circuit Sdn Bhd; Singapore; On-site; SGD 89,000 - 156,000; Full time

Job summary

Jabil Circuit Sdn Bhd is seeking a test engineering professional who independently develops, validates, and sustains production test systems for medical and in vitro diagnostic products. You will own assigned test processes and support manufacturing transfer, validation, and regulatory compliance activities.

Key duties include test development, NPI readiness, equipment qualification, and ensuring adherence to ISO 13485 and FDA 21 CFR Part 820 through IQ/OQ/PQ activities and traceability

Qualifications

• Experience with functional and system-level testing.
• Knowledge of test automation tools and scripting.
• Familiarity with ISO 13485 and FDA 21 CFR Part 820 is preferred.

Responsibilities

• Develop and optimize functional and system-level test solutions.
• Design or improve test fixtures, test station architecture, and measurement methods.
• Develop test software and automation scripts.
• Review product design for manufacturability and testability.
• Lead test readiness activities for assigned NPI programs.
• Support site-to-site transfer, customer transfer, and production release activities.
• Complete tester qualification and readiness before production launch.
• Support testing and troubleshooting of fluidics, optics, motion control, temperature control, sensors, and electronic subsystems.
• Validate instrument performance against customer and product specifications.

Skills

FVT, SLT knowledge

ICT expertise

test fixture design

statistical analysis

root cause analysis

Education

Bachelor Degree in Electrical/Electronics/Biomedical/Mechatronics or related Engineering

Tools

LabVIEW

NI TestStand

Python

Visual Basic

SQL

Job description

Jabil Circuit Sdn Bhd is seeking a test engineering professional who independently develops, validates, and sustains production test systems for medical and in vitro diagnostic products. You will own assigned test processes and support manufacturing transfer, validation, and regulatory compliance activities.

Key duties include test development, NPI readiness, equipment qualification, and ensuring adherence to ISO 13485 and FDA 21 CFR Part 820 through IQ/OQ/PQ activities and traceability