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Eitan Medical is a fast-growing global medical device company, developing and manufacturing innovative drug delivery and infusion solutions across the continuum of care: from the hospital to the home. As part of our growth and commitment to innovation , we are expanding our R&D department and looking for a Senior Mechanical Engineer to join our Mechanical team in the R&D department. Join us as we continue to grow and make a meaningful impact on healthcare worldwide Job Description Mechanical design of multidisciplinary medical devices (infusion pumps) and accessories with a focus on mechanisms’ development and injection molded plastics design. Drive all the mechanical aspects of design and development of new products, while supporting the company’s current product portfolio.

This position is responsible for designing and developing new and improved manufacturing processes and ensuring efficient and effective product transfer into production within the medical disposable devices industry.  Improve existing processes and implement new processes in the production line.

Job Responsibilities:

Develop and implement new manufacturing processes for production.

Perform Design of Experiments for process definition and optimize equipment parameters for new and/or existing processes.

Create documentation to support new and improved manufacturing processes.

Write and perform process validations (IQ, OQ, PQ) and validate methods for inspection, verification, and process controls.

Interface directly with assemblers, production supervisors, leads, and engineers.

Assesses process capabilities, innovates, and implements process improvements on key projects.

Applies technical knowledge to innovate, design, and develop processes, procedures, tooling, and/or automation.

Executes the functional deliverables associated with the NPI, Design Control, CAPA, and all Quality Systems.

As needed; plan, organize, and participate in all aspects of technical reviews.

Collaborate to ensure proper documentation is completed to meet quality systems requirements. (e.g., GOIs, BOMs, Routers, FMEAs, etc.).

To Equipment Engineer will be responsible to engineer and implement highly capable & effective manufacturing equipment to meet business goals and objectives.

Key Responsibilities:
Responsible for developing testing and manufacturing equipment.
Create mechanical designs and drawings using Solidworks according to department standards and company procedures.
Ensure relevant documentation is prepared in line with all Quality and Regulatory guidelines and promotes full compliance with all GMP & E&AS
Identifying and solving the root cause of complex technical issues with production equipment.
Writing and execution of equipment qualifications, protocols, and reports.
Implementation of equipment into the production lines.

a well-funded medical startup transforming ICU care through advanced technology and innovation. Our smART+ platform is an intelligent, sensor-based solution that optimizes nutrition delivery while reducing the risks of ventilator-associated pneumonia and malnutrition. Supported by clinical trials, we are setting a new standard in critical care by achieving nearly 100% feeding efficiency and reducing ICU stays by an average of 3.3 days. We are looking for a talented NPI Engineer to join our collaborative and growing engineering team. As a member of the team, the suitable candidate will perform the following tasks:
* Optimizing the manufacturing line for mass production, including mechanical design of new machines and jigs, identifying and addressing bottlenecks.
* Conducting failure investigations and implementing process improvements using various engineering methods (e.g., mechanical design, sheet metal, programmed controllers, etc.).
* Performing validations and developing detailed work instructions to support production and Quality Assurance processes.

Process Engineer Injection & Molding Engineering team
Description
Main missions & responsibility:
1. Injection Project management.
2. Managing equipment & purchasing projects (molds, injection machines...).
3. Leading significant projects in Injection, including checks and assimilation of new production technologies.
4. Injection department support with new equipment.
5. Engineering & technical support for the Injection departments.
6. Leading or partnering with production improvement processes.
7. Focal point for all technical Injection & mold matters.
8. Guiding and supporting Injection department engineers.
9. Managing existing suppliers and developing new ones.
Work location: Office, production halls, suppliers (in Israel and abroad), Netafim production factories. The job requires travel in Israel and abroad for time to time.

Required Process Engineer Injection & Molding Engineering team
Main missions & responsibility:
1. Injection Project management.
2. Managing equipment & purchasing projects (molds, injection machines...).
3. Leading significant projects in Injection, including checks and assimilation of new production technologies.
4. Injection department support with new equipment.
5. Engineering & technical support for the Injection departments.
6. Leading or partnering with production improvement processes.
7. Focal point for all technical Injection & mold matters.
8. Guiding and supporting Injection department engineers.
9. Managing existing suppliers and developing new ones.
Work location: Office, production halls, suppliers (in Israel and abroad), production factories. The job requires travel in Israel and abroad for time to time.

We are looking for a System Verification Engineer.
About The Position:
Define System Verification based on System (SW/HW) Design Inputs:
Study design/reliability requirements.
Take part in design reviews.
Define and execute feasibility experiments for proof of concept/design.
Establish Verification Equipment, Verification Methods and Infrastructure:
Define, develop, and maintain testing equipment and methods to provide the means to execute verification.
Collect and analyze data for improvement of methods/processes.
Plan and execute Design Verification and Process Validation for:
Developed products and processes.
Engineering Change Orders.
Service/Manufacturing equipment and processes.
Prepare and release Verification Reports:
Based on collected, analyzed data vs. pre-defined acceptance criteria.
In compliance with companys QMS and applicable standards/regulations.
Participate in the following forums:
Design reviews
Product development gates and milestones.
Initiate, manage, and monitor external testing contractors, such as Testing Houses and Labs.
Define and prepare testing to be performed by external contractors.
Identify and study relevant standards and guidelines (e.g. transportation/shelf-life standards).
Track, review and approve external testing reports.
Working according to Quality Policy, relevant Quality Procedures & Standards, and privacy & safety rules.