Manufacturing Engineer

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במקום לעבור לבד על אלפי מודעות, Jobify מנתחת את קורות החיים שלך ומציגה לך רק משרות שבאמת מתאימות לך.

מעל 80,000 משרות • 4,000 חדשות ביום
חינם. בלי פרסומות. בלי אותיות קטנות.

חברה בתחום מש"א / הדרכה / השמה / בתי תוכנ

מספר מקומות

חברה בתחום מש"א / הדרכה / השמה / בתי תוכנ

מספר מקומות
מלאה
12,000-17,000 ₪ (הערכה מבוססת AI)
הערכה מבוססת AI ולא שכר של המעסיק

Responsible for driving the transition of complex, multidisciplinary medical devices from design to sustainable serial production through the ECO process, as well as sustaining and optimizing active manufacturing lines.
The scope encompasses process design, yield optimization, system -level troubleshooting (mechanics, electronics), and strict adherence to medical device quality regulations (ISO 13485 / FDA 21 CFR Part 820).
High proficiency in drafting technical documents, Standard Operating Procedures (SOPs), and navigating Product Lifecycle Management (PLM) systems for bill of materials (BOM) management.
Multidisciplinary Troubleshooting:
Strong systems-level diagnostic skills to root-cause failures occurring at the intersection of mechanical, electrical, or firmware subsystems.
Validation Risk Management:
Practical proficiency in writing and executing validation protocols (IQ/OQ/P

Requirements:
Minimum of 2+ years of experience as a Manufacturing/Production Engineer within Medical Devices industry
Proven track record of executing Engineering Change Orders (ECOs) within a structured Quality Management system (QMS).
B.Sc. in Mechanical Engineering, Electrical Engineering, Biomedical Engineering, or Manufacturing Engineering from an accredited institution.
Fluent in English Hebrew

Advantage Experience:
Direct experience collaborating with external contract manufacturers (CMs) and suppliers on component and system level quality issues.

Familiarity with Arena and Priority systems

This position is open to all candidates.