חזרה ללוח
Manager, Manufacturing Engineering
MESH Executive
מיקום
שרון
תחום
מכשור רפואי
בכירות
ביניים
היקף משרה
משרה מלאה
גודל חברה
בינונית (51-200)
סוג תפקיד
ייצור
תיאור המשרה
MESH Executive Solutions has been retained by a leading, fast-growing global MedTech corporation to identify a highly accomplished Manufacturing Engineering Manager for their Israeli site.
Our client specializes in advanced contract manufacturing and the development of life-saving medical devices. Operating as a structured, tier-1 global partner to the world's largest medical device brands, the company seamlessly combines cutting-edge engineering centres with high-volume, mass-production facilities.
Position Overview: We are seeking a highly experienced, dynamic, and hands-on leader to head the local engineering department. This critical role balances advanced mechanical design, complex process execution, and high-volume manufacturing.
Key Responsibilities
• Engineering Leadership: Lead, mentor, and build a high-performing Manufacturing and process engineering team. Drive professional growth and accountability across all team members.
• NPI & Mass Production: Oversee the transition of complex medical products from prototyping/R&D stages into stable, high-volume mass production lines.
• Process Optimization: Drive deep technical understanding of advanced manufacturing processes, equipment validation, and production automation.
• Global Interface: Act as the primary technical and managerial interface with US-based corporate functions, global engineering teams, and strategic international clients.
• Execution & Deliverables: Set clear engineering KPIs, manage departmental budgets, ensure strict timeline adherence, and make critical engineering decisions under tight delivery pressures.
דרישות התפקיד
Education & Experience
B.Sc. in Manufacturing Engineering (or related engineering disciplines such as Materials - a strict requirement.
At least 3-5 years of proven experience in a managerial role leading a team of Manufacturing or process engineers within an industrial environment.
Industry & Regulatory Environment:
Minimum of 5 years of experience in the Medical Device (MedTech) industry – deep and practical familiarity with strict medical regulatory environments operating under ISO 13485 standards is mandatory.
Comprehensive experience with medical validation protocols (IQ/OQ/PQ) and risk management (FMEA).
Operational & Technical Depth:
Proven track record in Mass Production (High-Volume) or complex NPI (New Product Introduction) environments. Experience limited solely to early-stage startups, low-volume R&D, or theoretical research laboratories will not qualify.
Deep \"Hands-on\" process understanding: Strong technical background in modern manufacturing technologies (laser processing, multi-disciplinary assemblies, or metallurgy).
Global & Corporate Fit:
Substantial experience within a large, structured Global Corporation or large multidisciplinary company that enforces structured work methodologies, matrix reporting, and KPIs.
Proven experience working closely with overseas corporate headquarters (specifically US-based).
English - fluent level (both written and spoken) – ability to lead complex technical discussions and corporate presentations completely in English.
Leadership Profile:
Demonstrated \"Lead by Example\" approach: A manager who is active on the production floor, technically engaged in troubleshooting alongside the team, and possesses strong, decisive decision-making capabilities.
