דרושים » מדעים מדוייקים » Production Validation engineer

we are a fast-growing global medical device company that develops and manufactures innovative drug-delivery and infusion solutions across the continuum of care, from hospital to home. We are looking for an experienced V&V Manager to lead our V&V function and team within the R&D
Job Description
* Lead the V&V function and define the verification and validation strategy for new products and design changes.
* Manage, develop, and provide technical leadership to a multidisciplinary team of V&V engineers, including goal setting, workload allocation, mentoring, and performance development.
* Ensure complete, risk-based TEST coverage and traceability from product and system requirements through TEST evidence and final reports.
* Review and approve V&V plans, protocols, reports, deviations, and supporting technical documentation.
* Oversee system -level hardware, software, mechanical, and disposable-set testing in the R&D laboratory and at external laboratories and subcontractors.
* Lead experimental design, data analysis, structured problem-solving, and root-cause investigations.
* Plan resources, equipment, schedules, and priorities, and monitor execution against project milestones and quality objectives.
* Partner with Systems, R&D, Quality, Regulatory, Clinical, and Project Management teams, and provide V&V support during audits and regulatory submissions. Reports to: R&D Director

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 Staff GPU Verification Engineer
Join our GPU Hardware Verification team in Raanana, Israel, and help shape the future of the world's most widely deployed GPU architecture - Mali. As a Staff Hardware Verification Engineer, you will play a key technical role in verifying advanced GPU components and subsystems, working alongside architects, designers and verification engineers to deliver high-quality, industry-leading graphics technology. You'll contribute to complex verification environments, solve challenging technical problems and help drive continuous improvements to our verification methodologies and flows.
Responsibilities:
Develop and execute verification plans for advanced GPU components and subsystems.
Develop and maintain AI tools, agents, and skills to support our engineering teams and workflows.
Build, maintain and enhance robust verification environments using SystemVerilog and UVM.
Apply coverage-driven, constrained-random and, where appropriate, formal verification techniques to achieve comprehensive functional coverage.
Debug complex functional issues and work closely with Design and Architecture teams to identify and resolve root causes.
Contribute to block-level and system-level verification, including environment integration and regression analysis.
Improve verification methodologies, automation, scripting and continuous integration flows to increase quality and efficiency.
Participate in verification reviews and support verification sign-off activities.
Share technical knowledge and collaborate with colleagues across the wider GPU engineering organisation.