דרושים » הנדסה » Manufacturing Engineer

Join our company as a Mechanical Engineering Manager, play a key role in the design and development of innovative mechanical and electromechanical medical products and systems across Research and Technology (R&T), New Product Development (NPD), and Released Product Engineering (RPE). You will lead and develop a team of experienced Mechanical Engineers responsible for the R&D efforts within Cranial and Spinal Technologies Platform/Solutions organization. You will provide both people and technical leadership throughout the product lifecycle, from early concepts and feasibility through detailed design, verification, design transfer, production support, and post-market product improvements. The team operates in a highly regulated environment and is responsible for delivering safe, reliable, and high-quality mechanical and electromechanical solutions in accordance with applicable medical device development processes and Quality System requirements.
You will work in a global matrixed organization and collaborate regularly with colleagues, managers, technical experts, and cross-functional stakeholders across international sites. The role is responsible for directing professional employees, managing engineering functions, and driving business objectives. The role is primarily performed on-site in Caesarea due to the hands-on, hardware-oriented nature of the work.
Primary Responsibilities:
Lead, coach, and develop a team of Mechanical Engineers, including goal setting, performance management, regular one-on-one meetings, and career development.
Plan, prioritize, and direct mechanical engineering activities across sustaining engineering, platform improvements, and new product development.
Provide technical leadership for the development of complex mechanical and electromechanical medical devices from concept through verification, design transfer, and production readiness.
Ensure engineering activities and documentation comply with Design Control, Quality System requirements, internal procedures, and applicable medical device regulations.
Lead technical investigations, root-cause analysis, corrective actions, and improvements related to released products and production.
Manage resources and priorities across multiple projects while supporting program schedules, product quality, and business objectives.
Collaborate with global and cross-functional partners, including Systems, Electrical, Software, Manufacturing, Quality, Regulatory, Service, and Program Management.
Coordinate activities with suppliers, consultants, and manufacturing partners to support development, production, and timely delivery.

The Advanced Manufacturing Engineer (AME) is responsible for industrializing and sustaining complex PET and SPECT imaging products at a high‑complexity electromechanical manufacturing site. The AME ensures robust manufacturability of high‑level mechanical assemblies, electronics integration, wiring, detector modules, motion systems, and system‑level testing. The role drives process development, tooling, validation, DFM/DFA, quality improvement, and readiness for production and NPIs.
NPI Leadership for PET & SPECT Imaging Systems
Lead manufacturing readiness for new PET/SPECT products, including process layout, tooling development, and new equipment introduction.
Participate in design reviews and influence DFM/DFA/DFT across mechanical assemblies, detector modules, power systems, wiring harnesses, and electromechanical subsystems.
Translate design intent into controlled, stable manufacturing processes.
Coordinate ECO implementation and ensure smooth manufacturing release.
Assembly Process Development & Optimization
Develop robust assembly processes for mechanical and electronic integration, alignment, torque control, and detector installation.
Define and design manufacturing jigs, tools, fixtures, and lifting/handling solutions required for large subsystems.
Lead design/manufacture of equipment, tooling, and jigs internally or via suppliers to eliminate defects.
Drive LEAN manufacturing implementation and support continuous improvement.
Conduct PFMEA for existing and new processes.
Quality & Problem Solving
Drive product quality improvements by identifying manufacturing issues and implementing cost‑effective solutions.
Work with Production Associates to resolve manufacturing and quality problems.
Oversee corrective action implementation in production or suppliers.
Support RCA through structured failure analysis.
System Integration & Testing Support
Support integration/testing of assembled PET/SPECT systems including calibration, alignment, motion validation, detector gain calibration, and safety checks.
Work with System Engineering to define test protocols and acceptance criteria.
Troubleshoot system issues related to electromechanical assemblies.
Validation & Regulatory Compliance
Own IQ/OQ/PQ for equipment, tools, and manufacturing processes.
Ensure compliance with ISO 13485, ISO 14971, 21 CFR 820, IEC 60601, and internal QMS requirements.
Maintain strong documentation practices including control plans, validation protocols, and DHR/DMR accuracy.
Ensure traceability for critical parameters, torques, and calibration data.
Supplier & Cross‑Functional Collaboration
Collaborate with suppliers of mechanical assemblies, detector modules, wiring harnesses, and PCBs.
Lead technical discussions with suppliers for tooling, process capability, and quality issues.
Train and qualify production and supplier teams on processes and inspection/assembly methods.
EHS & Plant Compliance
Lead and support Environment, Health & Safety efforts aligned with site goals.
Ensure safe handling of large assemblies, HV systems, and radiation‑related components.