לוח משרות דרושים ייצור ותעשייה

We are looking for a highly motivated and experienced Mechanical Engineer who will join our mechanical team and be responsible for designing and maintaining our new and current products, focused on consumable wearable products.

The Mechanical Engineer will work on exciting projects to support our expanding portfolio of products related to our cancer treatment device from concept all the way through manufacturing, taking into consideration quality, regulation, cost-effectiveness, and manufacturing feasibility.

ESSENTIAL DUTIES AND RESPONSIBILITIES:.
PCB and PCBA design for HW engineering.
Multidisciplinary products.
Customized design and consideration of manufacturability as part of the design.
Rigorous analyses of designs using appropriate methods such as FEA and dimensional tolerance analysis.
Consider automated production requirements as part of the design.
Evaluate requirements and determine mechanical requirements for the design and development of consumables.
Drive component and integration testing to verify that prototypes and production components/constructs meet design intent.
Assess requirements and set the mechanical requirements for the design and development of consumables.
Provide the data for a full production file (3D files, drawings of mechanical parts, assembly drawings and instructions, BOM).
Contact and manage suppliers and subcontractors for manufacturing.
Liaising with suppliers and production sub-contractors.
Conduct relevant research.
Producing and implementing designs and test procedures.
Perform the actual testing, evaluating, measuring, modifying, and re-testing of the design.
Generate test reports and documentation.

We are looking for a Mechanical Technician who will join the mechanical engineering team, and be responsible for supporting the mechanical development of innovative medical devices and related applications.

The job holder will be involved in the product life cycle and support the design team through the life cycle.

Full-time position at our R&D center, Haifa, Israel.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
Supporting an engineering team for the design development, assembly, and testing of our devices and subsystems.
Responsible for manufacturing and assembling prototypes of wearable products, and cutting and assembling soft materials.
Testing electrodes for internal experiments.
Supporting mechanical products in our systems.
Perform in collaboration with the cross-functional development team to ensure that the system meets operational requirements.
Perform practical bench testing and debugging of the mechanical design.
Transferring feedback to the production of the devices.
Assembling prototypes of our devices in design and development.
Assisting in the verification and validation process of the devices.
Compliance with the design control process.
Collaborate with other team members, engineers, managers and product management teams to develop innovative solutions that meet market needs.
Responsible for the laboratory environment and equipment, and laboratory safety.
Supporting test equipment calibration.

As an Operations Quality Team Manager, you will lead Q&R activities in the system plant as a PQE team manager. You will be responsible for driving product quality improvements by leveraging statistics and data analysis techniques to enhance processes. Your role will involve close collaboration with production, manufacturing engineering, and suppliers to ensure process control, quality assurance, effective failure analysis, and continuous improvement.
Your role:
Provide clear vision and strategy for the PQE team, ensuring alignment with organizational quality goals.
Build and develop the capabilities of the quality team, fostering a culture of continuous improvement and collaboration.
Lead MRB activities, periodic quality reviews, and provide actionable insights.
Lead real-time manufacturing line investigations, identify root causes of issues, and ensure the implementation of corrective actions through comprehensive reporting and follow-up.
Implement and monitor production and process controls, including Process Validation (PV), Equipment Qualification (EQ), Control Plans, and pFMEA.
Maintain compliance with ISO 13485, FDA regulations, and other relevant standards.
Prepare for and support external audits (regulatory, customer) and perform internal pre-audits.
Act as a liaison between R&D and Operations to ensure a smooth transition during NPI and change management And work closely with Production, Supply Chain, and Manufacturing Engineering to improve overall quality performance.