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We believe in giving back to help those in need in the communities where we live and work. And are equally committed to creating a healthier environment and planet through our sustainability efforts.

Job Summary
In this hybrid fixed term role (2 days remote, 3 days in office), you will be part of the Materials & Biological Safety (MBS) team, responsible for creating and maintaining material data and biological safety information, for medical devices manufactured by our company. as Materials & Biological Safety Associate Specialist. You will be responsible for providing ongoing material and biological safety support for R&D and Engineering teams and regulatory submissions.

Essential Duties and Responsibilities
Local/site point of contact for internal employees, external clients and service providers regarding materials and biological safety of West Medical Devices platforms mainly VTD and V2B.
Support the design and development teams with materials research, evaluation, and selection. Liaise with Product Design, Validation & Verification and Project Managers/Leads to achieve project goals through high quality, accurate and timely completion of deliverables.
Responsible for directing external/third-party biocompatibility testing service providers and coordinate testing at external labs.
Coordinate, build and procure sample devices from the manufacturing plant for use in biocompatibility and/or chemical characterization evaluations.
Create (author) and/or review and approve biocompatibility test plans, protocols, and reports.
Create (author) and/or review and approve biological gap assessments for Medical Devices and manufacturing process.
Create (author) and/or review Biological Risk Assessment (BRA) /Toxicological Risk Assessment (TRA) in preparation for completing biocompatibility testing and chemical characterization programs.
Provide general ongoing materials and biological safety support with customer requests/inquiries, regulatory body or customer audits, and regulatory submissions.
Maintain thorough understanding of relevant ISO standards, quality system and laboratory testing accreditation requirements.

Required Senior R&D System Application Engineer (12 Months Contract)
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.
What will you do?
You will be part of an R&D team responsible for the development, integration, and validation of medical device systems. With a strong emphasis on hands-on development, data-driven engineering, with a problem-solving mindset. you will contribute to the full product development lifecycle - from the need, through signal processing and GUI development to system testing and clinical application. This role is designed for engineers who are passionate about building and refining medical device technologies in a multidisciplinary environment.
How youll make an impact:
Develop and improve medical device features within the portfolio as part of a multidisciplinary R&D team that includes mechanical, hardware, and software engineers. Main activities include - procedure development, algorithm development, GUI design and implementation, scripting, test automation, data acquisition, and data analysis and visualization.
Participate in the design and development of system-level features, supporting architecture decisions and translating clinical and functional requirements into working solutions.
Perform hands-on testing of medical device systems (implant systems, hardware, and software), including functional, integration, and exploratory testing to validate design performance and clinical readiness.
Lead test design efforts, including writing test cases, test procedures, and test reports. Collect, analyse, and summarize test data to support design decisions and issue investigations.
Execute and support test protocols in lab and simulated clinical environments. Accurately document results, observations, and issues to ensure traceability and compliance.
Collaborate with stakeholders and colleagues - including caregivers, R&D engineers, clinical specialists, marketing, and quality teams - to understand system behaviour, clinical workflows, and end-user needs, ensuring that developed solutions align with real-world application requirements.

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.