Senior IVD Process Engineer: Tech Transfer & Validation

Jabil Circuit (Singapore) Pte Ltd; Singapore; On-site; SGD 90,000 - 150,000; Full time

Job summary

Jabil Circuit (Singapore) Pte Ltd is seeking a manufacturing engineering leader to act as technical authority for medical device and IVD manufacturing operations. You will define end-to-end manufacturing architecture, lead technology transfer, and drive process validation and regulatory readiness across audits.

The role requires 5 to 8+ years in manufacturing/industrial engineering with 3+ years in medical device or IVD manufacturing.

Qualifications

• Bachelor degree in Engineering; advanced degree preferred but not mandatory.
• 5 to 8+ years of manufacturing, process or industrial engineering experience.
• 3+ years of medical device or IVD manufacturing experience preferred.
• Demonstrated ownership of NPI, validation, technology transfer and customer-facing technical activities.

Responsibilities

• Define end-to-end manufacturing architecture, production scaling and capacity planning.
• Lead technology transfer, manufacturing readiness and process standardization for new or transferred products.
• Lead complex root cause analysis using structured problem-solving methods; apply DOE and SPC.
• Define validation master strategy and approve IQ/OQ/PQ approach; lead validation risk assessment.
• Prepare the site for customer audits, ISO audits, FDA readiness reviews and regulatory inspections.
• Coach engineers and technicians; support RFQ, capacity model, line design and transfer execution.

Skills

Technical leadership

Manufacturing strategy

Process validation

Problem solving

DOE & SPC

Regulatory readiness

Education

Bachelor's degree in Engineering

Advanced degree preferred

Tools

IQ/OQ/PQ

Job description

Jabil Circuit (Singapore) Pte Ltd is seeking a manufacturing engineering leader to act as technical authority for medical device and IVD manufacturing operations. You will define end-to-end manufacturing architecture, lead technology transfer, and drive process validation and regulatory readiness across audits.

The role requires 5 to 8+ years in manufacturing/industrial engineering with 3+ years in medical device or IVD manufacturing.