Process / Manufacturing Engineer III (IVD / Medical Device)

Jabil; Singapore; On-site; SGD 90,000 - 130,000; Full time

Job summary

Jabil is seeking a technical authority for manufacturing processes and technology transfer across medical device and IVD operations. You will lead validation strategy, IQ/OQ/PQ, and regulatory readiness while guiding automation and advanced manufacturing initiatives.

Ideal candidates have 5–8+ years in manufacturing/industrial engineering, with exposure to NPI, process validation and cross-functional customer interfaces in a regulated setting.

Qualifications

• Bachelor degree in engineering with strong manufacturing experience.
• 5–8+ years in manufacturing/process/industrial engineering.
• 3+ years in medical device or IVD manufacturing preferred.
• Proven ownership of NPI, validation, tech transfer and customer-facing activities.

Responsibilities

• Define end-to-end manufacturing architecture, capacity planning and scaling.
• Lead technology transfer, manufacturing readiness and standardization.
• Develop automation strategy and evaluate advanced manufacturing technologies.
• Lead root cause analysis and cost/quality/improvement projects.
• Define validation master strategy and IQ/OQ/PQ approaches.
• Prepare site for ISO/FDA audits and regulatory inspections.
• Coach engineers/technicians and lead cross-functional problem solving.
• Support RFQ, line design, capital planning and transfer execution.

Skills

Root Cause Analysis

DOE

Process Simulation

Automation Strategy

Technology Transfer

Validation Leadership

Regulatory Readiness

Education

Bachelor Degree in Engineering

Advanced degree preferred

Tools

SPC

IQ/OQ/PQ

Process Simulation Software

Job description

Position Summary

Acts as technical authority for manufacturing processes, technology transfer, process validation, equipment strategy and operational excellence for medical device and IVD manufacturing operations.

Position Summary

Acts as technical authority for manufacturing processes, technology transfer, process validation, equipment strategy and operational excellence for medical device and IVD manufacturing operations.

Technical Requirements

Manufacturing Strategy

• Define end-to-end manufacturing architecture, production scaling strategy and capacity planning approach.
• Lead technology transfer, manufacturing readiness and process standardization for new or transferred products.
• Develop automation strategy and evaluate advanced manufacturing technologies.

Advanced Technical Skills

• Lead complex root cause analysis using structured problem-solving methods.
• Apply SPC, DOE, process simulation, operations research and business case analysis.
• Drive high-impact improvement projects involving cost, quality, output, reliability and manufacturability.

Validation Leadership

• Define validation master strategy and approve IQ/OQ/PQ approach.
• Lead process validation strategy, equipment qualification strategy and validation risk assessment.
• Prepare the site for customer audits, ISO audits, FDA readiness reviews and regulatory inspections.

Medical Device Regulatory Expertise

• Serve as SME for ISO 13485, FDA inspection readiness, MDSAP awareness, design transfer and process validation expectations.
• Review change control impact, CAPA effectiveness, risk assessment and technical file support needs.

IVD Manufacturing Expertise

• Lead manufacturing readiness for hematology systems, urinalysis analyzers, immunoassay platforms and molecular diagnostic instruments.
• Provide technical direction for automated sample handling, precision dispensing, optical measurement, fluidics and motion control processes.

Leadership and Customer Interface

• Coach engineers and technicians, lead cross-functional problem solving and represent manufacturing engineering in customer technical reviews.
• Support RFQ, capacity model, line design, capital planning and transfer execution.

Education And Experience

• Bachelor Degree in Engineering; advanced degree is 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.