Position Summary

Owns assigned manufacturing processes, drives yield improvement, supports NPI and manufacturing transfer, and leads validation activities for medical device and IVD products.

Technical Requirements

Advanced Manufacturing Engineering

•            Develop, optimize and sustain manufacturing processes for assigned product lines.

•            Support DFM reviews, assembly optimization, equipment qualification and workstation design.

•            Perform process capability studies and define improvement actions.

Lean and Continuous Improvement

•            Lead value stream mapping, DMAIC, Kaizen, waste elimination and OEE improvement activities.

•            Drive cost reduction projects through process simplification, layout improvement and equipment utilization.

•            Use data-driven methods to improve line efficiency, yield and production stability.

Validation Expertise

•            Own IQ/OQ/PQ activities for assigned equipment, processes or production areas.

•            Perform Gauge R&R, process capability analysis, risk assessment and FMEA updates.

•            Prepare validation reports, process release evidence and manufacturing readiness documentation.

Medical Device Compliance

•            Apply ISO 13485 and FDA 21 CFR Part 820 requirements in daily engineering work.

•            Support change control, CAPA, deviation management, traceability and DHR requirements.

•            Participate in internal audits, customer audits and regulatory readiness activities.

IVD-Specific Knowledge

•            Support processes involving fluidics assemblies, optics modules, motion control systems, reagent handling and environmental control requirements.

•            Troubleshoot process-related failures on IVD analyzers or medical device equipment.

Education and Experience

•            Bachelor Degree in Mechanical, Manufacturing, Industrial, Biomedical, Mechatronics or related Engineering.

•            3 to 5 years of manufacturing, process or industrial engineering experience.

•            2+ years of medical device, healthcare or IVD manufacturing experience preferred.

•            Experience supporting NPI transfer and validation activities.

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Jabil, including its subsidiaries, is an equal opportunity employer and considers qualified applicants for employment without regard to race, color, religion, national origin, sex, age, disability, genetic information, veteran status, or any other characteristic protected by law.

Accommodation Statement

If you are a qualified individual with a disability, you have the right to request a reasonable accommodation if you are unable or limited in your ability to use or access Jabil.com/Careers site as a result of your disability. You can request a reasonable accommodation by sending an e-mail to Always_Accessible@Jabil.com with the nature of your request and contact information. Please do not direct any other general employment related questions to this e-mail. Please note that only those inquiries concerning a request for reasonable accommodation will be responded to.