♦ Receive and establish production lines transferred from Israel to China, including process equivalency verification and pilot runs approved by Engineering Israel.
♦ Improve manufacturing processes on the local line — coordinated with Israel processes and approved by the Engineering Manager, per ECO procedure.
♦ Perform process re-validation (IQ/OQ/PQ) following changes in equipment, location, or parameters, including protocols and reports for approval by Israel.
♦ Support NPI activities for products localized at China sites & CMO`s - stage-gate participation, local pilot builds, DFM feedback to Engineering Israel.
♦ Manage production nonconformances (NCR): containment, segregation, root cause investigation, corrective actions (CAPA), and return-to-production support in coordination with QA and Engineering Israel.
♦ Identify and evaluate local suppliers, including supplier audits and assessment reports.
♦ Technical management of subcontractors: process control, specification compliance, performance monitoring.
♦ Responsible for translation and adaptation of production documentation for the local line (work instructions, drawings, inspection specifications), aligned to the controlled revision of source documentation.
♦ Full member of the Engineering team — when local workload permits, receives assignments from the Engineering Manager, Israel. Structured weekly report: line status, open nonconformances, risks.
RequirementsEducation, Courses & Certifications
♦ B.Sc. in Mechanical / Industrial / Materials Engineering — required.
♦ Training in process validation or quality control — advantage.
Professional Experience & Knowledge
♦ 3+ years of manufacturing engineering experience in an industrial environment — required.
♦ Experience in assembly processes of mechanical / pneumatic / electromechanical systems.
♦ Knowledge and experience in reading and interpreting drawings, electrical and pneumatic schematics, GD&T.
♦ Knowledge and experience operating various measurement tools.
♦ Experience performing validations (IQ/OQ/PQ) and failure investigation (8D, 5-Why).
♦ Proficiency in OFFICE software; ability to prepare and write technical documents in English.
♦ Experience in production transfers / line ramp-up — advantage.
♦ Experience in medical devices or regulated industry (ISO 13485 / GMP) — significant advantage.
♦ Experience working in an ERP environment, especially PRIORITY — advantage.
♦ Experience working with foreign companies / international teams — advantage.
Languages
♦ Mandarin — native / full proficiency — required.
♦ English — high proficiency, including technical English (reading, writing, speaking) — required (working language with Israel).
Skills Required
- B.Sc. in Mechanical, Industrial, or Materials Engineering
- Training in process validation or quality control
- 3+ years manufacturing engineering experience in an industrial environment
- Experience in assembly processes of mechanical, pneumatic, electromechanical systems
- Ability to read and interpret drawings, electrical and pneumatic schematics, GD&T
- Experience operating various measurement tools
- Experience performing validations (IQ/OQ/PQ) and failure investigations (8D, 5-Why)
- Proficiency with Office software and ability to prepare technical documents in English
- Experience in production transfers / line ramp-up
- Experience in medical devices or regulated industry (ISO 13485 / GMP)
- Experience working in an ERP environment, especially PRIORITY
- Experience working with foreign companies / international teams
- Mandarin native / full proficiency
- High proficiency in English including technical reading, writing, and speaking
What We Do
Mego Afek is an Israeli medical-device developer and manufacturer specializing in pneumatic compression therapy systems. Founded at Kibbutz Afek, it applies decades of pressure-technology expertise to products for lymphedema, venous insufficiency, peripheral arterial disease, and deep-vein thrombosis prevention. The company also develops aesthetic, sports-recovery, and rehabilitation solutions, manufacturing its products in-house at its Northern Israel facilities for clinical and therapeutic use worldwide.
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