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our company 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. We are looking for an excellent Research Engineer to join the R & D team. Job Description Lead novel research in state-of-the-art technologies - bypass technological borders Lead departmental tasks that include problem solving and critical/root cause analysis Algorithms development for various system components Design and implementation of experiments for various projects Manage mutual research projects done and universities around the world

Responsibilities
Support the maintenance and organization of the Design History File (DHF) documentation.
Assist in completing documentation required for product releases in compliance with FDA, CE, ISO, and internal procedures.
Provide administrative support for design control activities throughout the product development lifecycle.
Support documentation related to software validation and traceability.
Assist in preparing documentation for audits and regulatory submissions.
Ensure documentation is accurate, complete, and properly filed in internal systems.

We are seeking a highly motivated and experienced Sr. Production and Quality Engineer to drive exceptional product quality, patient safety, and field reliability across the Installed Base (IB). This is a key technical role supporting production stability, RMA/DOA investigations, Automated Test Equipment (ATE) performance, and cross-functional quality engineering initiatives in a regulated medical device environment
Key Responsibilities
In this role, you will
Support RMA/DOA processes and continuous reduction of field failures.
Support qualifications and control of ATE testers in production lines.
Support ECO/ECR processes, NPI projects, product updates, and cross-functional engineering changes.
Work closely with R&D, engineering, manufacturing, and operations teams to enhance product quality and resolve technical issues.
Drive continuous improvement initiatives using tools such as Six Sigma, Lean, and Root Cause Analysis (RCA).
Participate in supplier selection and conduct suppliers audits.
Ensure compliance with ISO 13485, FDA 21 CFR 820, MDR, and other applicable medical device regulations.
Maintain and support quality documentation, including CAPA, Non-Conformance Reports (NCRs), and risk management documentation.

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. We are looking for an excellent Research Engineer to join the R & D team.
Job Description:
Lead novel research in state-of-the-art technologies - bypass technological borders
Lead departmental tasks that include problem solving and critical/root cause analysis
Algorithms development for various system components
Design and implementation of experiments for various projects
Manage mutual research projects done and universities around the world
Direct Manager: Research director.

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. We are looking for an excellent Production Quality Engineer to join the QA product team.
Job Description:
Serve as owner of the NCMR process: manage the end-to-end handling of non-conforming materials, products, and processes, including initiation, investigation and corrective/preventive actions in accordance with company procedures and regulatory requirements.
Monitor NCMR process including quality KPIs
Support for non-conformity investigations and assign effective corrective actions for NCMRs and ensure timely closure and documentation.
Perform / review Root Cause Analysis as part of NCMR process and assign relevant corrective actions.
Act as QA representative for Manufacturing Quality process
Conduct quality assurance activities such as data analysis and statistical evaluations, SOP review and approvals, audit preparation
Direct Manager: Manufacturing Quality Manager

ART MEDICAL is a fast-growing medical startup developing breakthrough solutions that improve patient safety and clinical outcomes in intensive care units worldwide. Our smART+™ platform is redefining critical care by optimizing nutrition delivery and reducing ICU stays through advanced sensor-based technology. We are looking for a talented Mechanical Engineer to join our multidisciplinary engineering team and take part in developing cutting-edge medical devices from design to production. In this role you will: ? Design mechanical equipment for mass-production lines ? Create and maintain engineering documentation (ECOs, validations, work instructions, routing cards, etc.) ? Improve production processes and support manufacturing activities ? Collaborate with cross-functional teams in a dynamic and innovative environment

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. We are looking for an excellent Research Engineer to join the R & D team. Job Description · Lead novel research in state-of-the-art technologies - bypass technological borders · Lead departmental tasks that include problem solving and critical/root cause analysis · Algorithms development for various system components · Design and implementation of experiments for various projects · Manage mutual research projects done and universities around the world Direct Manager: Research director

This role offers an exciting opportunity to contribute to the development of innovative delivery systems and support clinical investigations and complaint handling, partnering with QA and Clinical Development that will revolutionize the treatment of cardiovascular diseases.

How you will make an impact: 

As an R&D Engineer, Provides expertise in the optimization of product development for the Innovalve delivery system and accessories.

Design and Development: Design, analyze, and develop components and processes that meet stringent quality, performance, and regulatory requirements.

Problem-Solving: Identify and troubleshoot complex technical issues that arise during development and clinical trials.

Custom Solutions: Develop tailored solutions for unique design challenges and clinical requirements

Lead and perform product investigations for returned products and complaint samples, including hands-on functional evaluation, data collection and custom testing setup development.

Analyze investigation data to determine probable root cause and contributing factors using structured problem-solving methods (e.g., 5-Why, Fishbone).

Prepare clear technical summary reports and present investigation results to cross-functional teams; track actions to closure.

Work closely with Quality Assurance to support complaint handling workflows, ensure investigation documentation is complete, and align on conclusions and next steps.

Follow up on complaints arising from clinical cases (e.g., case questions, device performance observations) and provide timely technical input to R&D, QA and Clinical Development teams.

Collaborate with cross-functional partners to define and implement corrective actions addressing issues identified through investigations.

Support change management activities (e.g., ECOs) and contribute to risk management updates as needed based on investigation learnings.

Clinical procedure experience - Advantage.

Required Senior System Engineer
Job Description Summary
As a Senior System Engineer, you will play a critical role in the design, development, integration, and verification of complex medical imaging systems. You will be responsible for translating clinical needs into technical requirements, ensuring the robust performance, safety, and regulatory compliance of our innovative healthcare solutions.
Job Description
Job Responsibilities
Lead and participate in the full product lifecycle, from concept and requirements definition through design, development, testing, and deployment of medical imaging systems.
Translate high-level clinical and user requirements into detailed system and subsystem specifications, ensuring traceability and comprehensive coverage.
Perform complex system analysis, modeling, and simulation to optimize system performance, identify potential risks, and propose innovative solutions.
Collaborate closely with cross-functional teams including hardware, software, clinical, quality assurance, regulatory, and manufacturing engineers to ensure seamless integration and successful product delivery.
Define and execute system verification and validation plans, including test protocols, data analysis, and reporting, to ensure compliance with medical device regulations (e.g., FDA, CE).
Conduct root cause analysis for system-level issues, propose effective corrective actions, and drive their implementation.
Contribute to the continuous improvement of system engineering processes, tools, and methodologies within the organization.
Mentor junior engineers and provide technical guidance on complex system engineering challenges.
Stay abreast of industry trends, emerging technologies, and regulatory changes relevant to medical imaging systems.

We are seeking a highly motivated AI Product Owner to define, consolidate, and prioritize cross product inputs for a unified clinical AI capability. This role focuses on gathering and synchronizing requirements from multiple Product Managers and ensuring that AI features are designed to be as system level and agnostic as possible. Join us to help build scalable clinical AI that impacts healthcare at its core.
Job Description
ResponsibilitiesPartner with Product Managers across various product lines to collect, analyze, and consolidate clinical AI needs into unified feature level requirements.
Ensure consistent prioritization of AI requirements based on clinical impact, product strategy, and technical feasibility.
Maintain an ongoing feedback loop with Product Managers to refine requirements, capture gaps, and adapt prioritization as products evolve.
Translate cross product needs into clear, structured definitions, user flows, CTQs, and feature specifications for the AI R&D team.
Ensure alignment and consistency of requirements across teams to support development of an AI agnostic clinical capability.
Collaborate with AI, Data, Clinical and UX functions to ensure requirements are fully understood, feasible, and traceable.
Identify requirement-level risks, inconsistencies, or conflicts and drive resolution with relevant stakeholders.
Maintain clear documentation of requirements, rationales, and prioritization decisions to support transparency and regulatory processes.

Required Senior Manager PET V&V
Job Description Summary
The PET V&V Manager will lead and oversee all Verification and Validation activities for Positron Emission Tomography (PET) systems and components, ensuring product quality, regulatory compliance, and successful product launches within
Job Description
Job Responsibilities:
* Lead and manage a group of 30-40 V&V engineers and technicians, including team leads, with responsibility for hiring, training, performance management, and career development.
* Develop, implement, and maintain comprehensive V&V strategies, plans, and protocols for PET systems, subsystems, and software, adhering to our quality systems and regulatory requirements (e.g., FDA, CE).
* Oversee the execution of V&V activities, including test case development, test execution, defect management, and results analysis, ensuring thorough coverage and traceability to requirements.
* Collaborate closely with R&D, System Engineering, Quality Assurance, Regulatory Affairs, and Project Management teams throughout the product development lifecycle to define requirements, design testability, and ensure V&V deliverables are met on time and within budget.
* Drive continuous improvement in V&V processes, tools, and methodologies, incorporating industry best practices and lessons learned.
* Review and approve V&V documentation, including test plans, reports, and traceability matrices, ensuring accuracy and completeness.
* Participate in design reviews, risk assessments, and post-market surveillance activities to identify potential V&V implications.
* Represent the V&V team in internal and external audits, providing evidence of compliance and addressing any findings.
* Stay abreast of new technologies, industry standards, and regulatory changes relevant to PET imaging and V&V.

Required V&V Intern
Job Description Summary
Responsible for running various verification activities on PET medical products that covers multi-disciplinary aspects from SW/HW, electronics, mechanics, physics, image quality and radiation - which is safety for users and monitored by a tag all the time.
Job Description
Responsible for planning and implementing verification methodologies and ensuring proper fulfillment of system and sub-system requirements.
Responsible for reviewing various product designs, verifying its functionality in agile testing methods.
Responsible to determine the testing environments and tools.
Analyze and debug system failures and issue found during testing, while delivering detailed reports identifying these issues for further investigation.
Work closely with development teams
Non-hybrid, full-time position on site
Flexible on working hour, including 2-3 evening shifts (14:00-23:00) per week as needed
Working on global programs that required tight collaboration with global and Israel teams.

We are seeking a Lead Systems Engineer to drive Point-of-Care Ultrasound systems engineering activities across the full product lifecycle.
Job Description
Key Responsibilities:
Lead and manage system-level requirements and specifications throughout product development
Drive system verification and validation activities, including end-to-end system testing
Act as the primary interface between Algorithm, Software, and Verification & Validation (V&V) teams
Lead product risk management activities in accordance with regulatory and quality standards
Drive resolution of complex technical issues to ensure project milestones and goals are met
Collaborate closely with Program Management to support scheduling, mitigate technical risks, and inform decision-making through sound engineering judgment.

We are seeking a highly motivated System Engineer to contribute to the design, development, and integration of cutting-edge medical imaging systems. This role involves ensuring system performance, reliability, and compliance with medical standards.
Job Description
Job Responsibilities
Define and analyze system requirements, translating them into detailed technical specifications for hardware and software components.
Participate in the architecture, design, and integration of complex medical Ultrasound imaging systems .
Develop test plans and procedures to verify and validate system functionality, performance, and reliability.
Conduct root cause analysis for system defects and anomalies, implementing effective solutions and preventative measures.
Collaborate with cross-functional teams, including R&D, manufacturing, quality assurance, and regulatory affairs, throughout the product lifecycle.
Perform risk analysis and contribute to the development of mitigation strategies in accordance with medical device regulations.
Support the entire product development process, from concept to post-market surveillance.
Document all phases of the system engineering process, including requirements, design, test results, and issue resolution.
Stay abreast of new technologies and industry trends in medical imaging and system engineering.

Required V&V Engineer
Job Description Summary
Responsible for running various verification activities on PET medical products that covers multi-disciplinary aspects from SW/HW, electronics, mechanics, physics, image quality and radiation - which is safety for users and monitored by a tag all the time.
Job Description:
Responsible for planning and implementing verification methodologies and ensuring proper fulfillment of system and sub-system requirements.
Responsible for reviewing various product designs, verifying its functionality in agile testing methods.
Responsible to determine the testing environments and tools.
Analyze and debug system failures and issue found during testing, while delivering detailed reports identifying these issues for further investigation.
Work closely with development teams
Non-hybrid, full-time position on site
Flexible on working hour, including 2-3 evening shifts (14:00-23:00) per week as needed
Working on global programs that required tight collaboration with global and Israel teams.