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Rapid Medical is a fast-growing medical device company focused on developing, manufacturing, and selling innovative devices for endovascular interventional procedures. We are seeking a talented QA/RA Engineer to join our quality and regulatory team, playing a dual role that ensures our products meet the highest quality standards while navigating complex global regulatory requirements.
SCOPE & RESPONSIBILITIES Quality Assurance • Manage ECOs: conduct risk assessments, update relevant DMR documents and carry out necessary IQ, OQ, PQ activities if required, finalization of implementation tasks. • Manage DCOs in the PLM system: write and update QA procedures to ensure compliance with quality standards and regulatory requirements. • Manage NCR and CAPA processes: lead, write and supervise the NCR and CAPA processes, ensuring timely and effective resolutions. • Manage QA production activities: provide quality support to production operations, addressing deviations and non-conformities to maintain high product quality. • Ensure timely resolution of quality issues: promptly address all identified or assigned quality issues to prevent delays and maintain efficient operations. • Participate in internal and external audits, such as FDA inspections and notified body audits based on ISO 13485, EU MDR, and MDSAP requirements. • Supplier Quality Management: manage supplier qualification and performance monitoring, including SCAR management, and support supplier audits.
Regulatory Affairs • Prepare, coordinate, track, and follow up on submissions for medical devices across various international markets. • Prepare and manage EU MDR technical documentation submissions. • Oversee CER, PMS, and PMCF activities, including customer complaints, vigilance, and recall. • Participate in regulatory inspections and audits. • Prepare regulatory assessments for design changes. • Develop labeling according to applicable regulatory requirements. • Evaluate and communicate regulatory impact of ECOs and design changes across QA and RA domains.

We are looking for an NPI Engineer for the R&D team. The NPI Engineer will own the end-to-end transition of multidisciplinary medical devices from R&D prototypes to stable, scalable serial production, serving as the bridge between product development and Operations.

If you want to work in an innovative, international environment and help push the boundaries of healthcare, well-being, and energy-based technology, this is your opportunity!


Key responsibilities:

Lead the full NPI and design-transfer process from R&D handoff through pilot builds, qualification, production ramp-up, and stabilization.

Build and drive transfer plans, schedules, risk and action tracking, production-readiness criteria, and release gates.

Create and maintain the manufacturing package, including BOM/DMR content, drawings, work instructions, test methods, acceptance criteria, tooling, and training materials.

Lead DFM, DFA, and DFT reviews and drive design and process improvements that support quality, manufacturability, serviceability, and cost.

Define, develop, and qualify manufacturing processes, fixtures, equipment, and test setups; prepare and execute validation protocols where applicable.

Lead ECOs and configuration changes, and provide hands-on support for production, yield, quality, field, and obsolescence issues using structured root-cause and corrective-action methods.

Serve as the technical focal point across R&D, Operations, QA/RA, Supply Chain, Service, suppliers, subcontractors, and contract manufacturers.

Within this operating model, the Turn-Key Account Manager plays a critical and central role in the companys supply chain.

Basic Job Purpose:
Acting as the primary interface between us and its subcontractors. The role ensures full execution of the supply process, including forecast alignment, production planning, purchase order management, and on-time delivery performance, while leading all operational, quality, and engineering issues to resolution across multiple stakeholders.


Main Duties:

Lead the day-to-day activities related to build-plan fulfillment monitoring.

Overall responsibility for Subcontractors/vendors OTD to comply with the company demands.

Lead to final resolution product quality and engineering issues.

Implementing new products (as part of NPI).

Lead Quarterly Business Reviews process and meetings.

ECO implementations.

Sub-contractor Capacity monitoring.

Price list management & monitoring.

OBS & Critical parts tracking.

Inventory counts at vendors once a quarter.

We are looking for a Technical Project Engineer for the Engineering team. The Technical Project Engineer will be responsible for leading Engineering projects for cost-reduction & sustain engineering

If you want to work in an innovative, international environment and help push the boundaries of healthcare, well-being, and energy-based technology, this is your opportunity!

Main Duties:

Leading Advanced Engineering Projects for Medical multidiscipline system, focusing on value engineering and BOM (Bill of Material) cost-reduction efforts.

Leading E2E (End-2-End) Projects ECO's, from PoC/E (Proof of Concept/Experiment) thought design & Testing (V&V), up to NPI and Production implementation.

Write and Execute Design Verification Testing (V&V) for cost-saving & Sustain engineering projects.

Updating/Creating the BOM & DMR of the System within project in the PLM system.

Write and Execute Manufacturing Validation Testing (PV/MP) from planning through execution & implementation in production sites.

Quality Gate Keeper ensuring overall device safety, efficacy and compliance are withstanding the overall system quality level.

We are looking for a proactive, self-motivated Project Engineer to join our cross-platform team. In this role, you will lead and execute a variety of sustain engineering projects and activities, including cost reduction initiatives, creation of new product configurations, and updates to existing configurations driven by regulatory requirements or process improvement needs. You will work closely with cross-functional stakeholders, primarily from RA, Engineering, R&D, and QA.

Manage and execute cross platform projects from initiation to implementation phase while working with internal and external resources.

Create and maintain new product configurations in our PLM system and verify proper transfer to production and implementation.

Perform changes to existing products, update work instructions, test procedures, labeling etc.

Lead process validation activities in our production lines (sub-contractors).

Manage the Engineering Change Order (ECO) process, end to end.

Participate in miscellaneous engineering department activities as needed.

We are looking for a Clinical Manager to join our Aesthetics Business Unit, which includes a broad portfolio of leading market solutions as well as an exciting innovation pipeline.

The Clinical Manager will be responsible for pre-market and post-market clinical activities for the assigned platform, including defining clinical requirements to guide design input, leading pre-clinical validation planning and execution, providing clinical input to regulatory submissions, supporting market conditioning for new solutions, generating post-market clinical evidence, and developing relationships with key opinion leaders.

This role is a key pillar in demonstrating the clinical value, safety, performance, and benefits of our solutions, while strengthening relationships with global KOLs, clinical investigators, and cross-functional stakeholders.

Key responsibilities:
Develop and manage end-to-end clinical project plans, timelines, and budgets, from early clinical research and pre-clinical validation through clinical trials, publications, user guidelines, and post-market evidence generation.
Drive cross-functional collaboration across multiple interfaces and business units.
Conduct deep clinical and scientific assessments, including review of the standard of care, clinical trends, mechanism of action, and emerging technologies, to support current and future product development and innovation.
Define pre-clinical validation strategies and lead pre-clinical evaluation activities.
Lead the strategy, planning, and execution of clinical studies, ensuring adherence to study protocols, ethical requirements, Good Clinical Practice, regulatory requirements, timelines, and budgets.
Form and cultivate strong collaborative relationships with cross-functional partners in R&D, product management, marketing, regulatory affairs, quality assurance, clinical training, and regional commercial teams.
Lead clinical input and support for key regulatory submissions and processes, including clinical rationales, clinical validations, clinical evaluation reports, and clinical development plans.
Support marketing and commercial activities from a scientific and medical perspective, including review and input into marketing collateral, development of white papers, clinical summaries, presentations, training materials, and active participation in scientific meetings.
Communicate project status to stakeholders, providing clear updates on milestones, deliverables, risks, mitigation plans, and key decisions.

About the Role Our Engineering team leads the bridge between technology, innovation, and design to production. We aim to provide high-quality, professional service by preventing issues in advance and solving them in real-time. We are looking for a hands-on ATE Electronic Engineer with extensive experience in developing electrical cabinets to interface with testing instruments (Bed of Nails, ICT, Spectrum Analyzer). In this role, you will collaborate with Mechanical and Software engineers to define, design, develop, test, debug, and maintain electronic modules for automatic testing systems.
Responsibilities
* Repair of test stations
* Installing new stations in the line
* Perform electronic failure analysis process for company's products
* Determine root cause for failures under investigation and determine corrective actions with the production team

we are looking for a Head of System Engineering.
What will You do?
● Lead, manage, and develop a team of Systems Engineers and Verification & Validation (V&V) Engineers.
● Oversee a full development cycle process of a multidisciplinary system.
● Implement, guide and enhance system engineering and verification methodologies.
● Build and manage multi-project development working plans.
● Control system requirements settings with traceability to MRD.
● Develop and proof a complex, cross-functional system containing Robotic, Mechanical, Electrical, Software, and Algorithm aspects.
● Explore and define solutions and architectures through methodological system engineering tools and know-hows, in a lean fashion.
● Collaborate with the research, engineering, operations, procurement, and NPI teams.
● Coordinate with clients engineering teams and management to ensure efficient implementation and deployment of the product.

We are looking for a highly hands-on Practical Electronics Engineer to join our Manufacturing Engineering team.
The role focuses on developing and maintaining manufacturing test equipment and jigs, troubleshooting electronic and multidisciplinary systems, supporting production and NPI activities, and improving manufacturing processes throughout the product lifecycle.
Responsibilities:
Design, build, validate, and maintain electronic test jigs, fixtures, programming stations, and manufacturing test equipment.
Troubleshoot electronic assemblies, cables, test equipment, and production failures, and support root-cause analysis and corrective actions.
Define test methods, procedures, and acceptance criteria for assemblies and sub-systems.
Prepare wiring instructions, cable drawings, schematics, and technical documentation for production and training.
Support product development, prototype builds, NPI, production ramp-up, and mass production.
Provide DFM/DFT feedback and support system integration, verification, and production testing.
Collaborate with R&D, mechanical, software, quality, operations, production teams, and external suppliers.
Improve product and process quality by enhancing test coverage, equipment reliability, manufacturing processes, and key production KPIs.

We are looking for a Senior Electronics Practical Engineer to join our R&D team and play a key role in bringing our BeeHome robotic hive systems from development to mass production.
This is a highly hands-on role, working closely with mechanical, software, NPI, QA, and operations teams on integration, debugging, and production readiness of complex electromechanical systems.
What You'll Do:
Integrate electronic systems into robotic machines, including embedded boards, motion, communication, and power systems
Debug and troubleshoot analog and digital boards at component and system levels
Design, document, and support cable harnesses for production (schematics, pinouts, routing, labeling)
Lead design transfer to manufacturing, including BOMs, documentation, and ongoing production support
Design and build test setups, fixtures, and validation tools for development and production
Support existing board designs and new product revisions
Work closely with subcontractors, manufacturers, and assembly partners
Perform root-cause analysis on production and field failures and drive corrective actions
Collaborate with R&D, mechanical, software, QA, and operations teams throughout the product lifecycle

DRS RADA Technologies , a leading defense company developing and manufacturing life-saving radar systems, is looking for an MRO Operator to join our site in Beit She’an. Job Description:
* Perform functional testing of electronic boards using both manual and automated testing methods, utilizing advanced test equipment such as a multimeter, spectrum analyzer, and signal generator.
* Work with computerized systems to analyze test results, troubleshoot failures, and identify faults in accordance with strict procedures and quality standards.
* Analyze and repair electronic boards with complex failures.
* Identify faults and work with electronic schematics and circuits down to the component level.
* Full-time position: Sunday–Thursday, 08:00–17:00, with overtime and Friday work as required.

our company, a leading defense company developing and manufacturing life-saving radar systems, is seeking a student role within the Supplier Quality team. The position includes supporting Quality Assurance activities with suppliers in Israel and abroad, analyzing quality data, handling nonconformities, and supporting continuous improvement processes to ensure compliance with the companys quality requirements. Responsibilities
* Monitor supplier performance using quality metrics
* Handle nonconformance reports and quality deviations with suppliers
* Collect, analyze, and present quality data
* Maintain and update quality documents, procedures, and records in the companys systems