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DRS RADA is a global pioneer of RADAR systems for active military protection, counter-drone applications, critical infrastructure protection, and border surveillance. We are looking for a motivated and experienced Supplier Quality Engineer to join our team! As a Supplier Quality Engineer, you will be responsible for managing supplier programs for manufacturing and ensuring that quality programs follow regulatory requirements. Supplier Quality Engineer duties and responsibilities
* Driving supplier quality performance, including new product development and product quality improvement
* Providing leadership and management for the supplier quality department
* Ensuring the supplier meets all regulatory and company requirements.
* Performing quality system audits
* Establishing quality control objectives & Maintaining supplier quality records
* Promoting initiatives to improve quality.

Required R&D V&V Engineer (Maternity Leave Replacement)
Innovation starts from the heart. We put patients first. We invest a significant proportion of our revenue towards research and development to drive and develop groundbreaking medical innovations for structural heart disease. As part of our R&D Engineering team, you will work closely with our Quality and Manufacturing teams to develop the latest tools and technologies to address significant, unmet clinical needs that impact patients lives around the world.
This is a contract position for 8 months (Maternity Leave Replacement)
How you will make an impact:
You will have a leading role within a small team of expert engineers and technicians, working closely with global R&D and testing teams at our new state-of-the-art R&D center in Caesarea.
Design and execute bench tests as part of R&D projects: collect inputs, translate them to design specifications, design test systems, run tests, and validate the systems.
Lead, coordinate, and participate in cadaver and animal studies.
Perform research activities (review and search for clinical papers and publications).
Collaborate closely with QA on systems validation, test plans, test method validations, and study protocols and reports.
Maintain clear, structured, and traceable documentation of all test data, results, and records.
Interface with USA headquarters (travel 1-3 times a year; evening phone calls).
Organization and rigor are at the heart of this role. We work in a testing environment where the integrity and traceability of data is paramount.

We are seeking a highly creative, hands-on and technically strong R&D Engineer with 10-12 years of experience to lead the development of breakthrough concepts and emerging technologies for future minimally invasive therapies.
This role focuses on transforming ideas into viable product concepts and driving rapid learning cycles through prototyping, testing and multidisciplinary collaboration. The successful candidate will thrive in highly ambiguous environments and play a key role in shaping future product pipelines.
How you will make an impact:
Lead early-stage innovation activities, including concept generation, ideation, and feasibility assessment.
Develop and mature novel device concepts for minimally invasive therapies, including implants, delivery system and enabling technologies.
Design, build and test proof-of-concept prototypes, enabling rapid iteration and technical risk reduction.
Translate clinical needs into engineering solutions, integrating procedural and anatomical considerations into early designs.
Develop testing tools, benchtop models, and simulation platforms that replicate relevant anatomical and physiological conditions to evaluate device performance and procedural feasibility.
Plan and execute feasibility studies, bench testing, and design evaluations to validate technical concepts including pre-clinical studies.
Analyze test results, perform root-cause investigations, and drive design improvements based on engineering findings and clinical feedback
Drive design iterations based on testing results, failure analysis, and clinical feedback
Manage interfaces with global R&D teams, external partners, consultants and suppliers
Document technical findings, experimental results and engineering recommendations in a clear and structured manner.

our company is an international Medical Device company that develops and manufactures innovative medical equipment. Specifically, we develop infusion pumps and their related accessory products. Job Description: supplier approval/disapproval including supplier maintenance and issuance of the Approved Supplier List. Leading the SCARS process including SCAR initiation, SCAR follow up, Supplier investigation approval including root cause analysis and SCAR closure. Leading the supplier audits process (including initial and surveillance audits) for critical suppliers, service centers, laboratories etc. by conducting on site / remote audits. Issuance and execution of the supplier audits plan including supplier audits follow up and supplier non-conformance follow up and response approval.
* Support the execution of service agreements, quality agreements with suppliers and service centers. Leading the supplier score card process, including trending.
* Serve as  CAPA Coordinator and Subject Matter Expert
* Responsible and accountable for CAPA ownership, timely execution, and effectiveness of CAPAs. This includes creation, collaboration with functional teams on Problem Statement writing/Scope identification/Risk Assessment/Containment/Correction/CAPA plans/Verification of local and global compliance to CAPA procedures to ensure timely effective closure of CAPAs Generate data and key quality trending information for use in periodic reviews like Quality Metric Reviews and Management Review for CAPA and supplier processes.
* Work within, and ensure adherence to Quality system procedures, work instructions and other Quality system requirements.
* Write, update, release, and sign quality documentation within the Quality management system
Direct manager: QA Compliance Manager