דרושים » ביוטכנולוגיה » Verification and Validation Engineer

We are looking for a Validation & Verification clinical engineer to join our team. As part of the role, you will work closely with R&D to specify, execute, and report the required tests, as well as with QA / RA to ensure that the medical QMS complies. In this role, you will play a key role in ensuring the quality and reliability of our products through rigorous testing and validation. A strong technical background, excellent problem-solving skills, and the ability to work collaboratively with various teams are required for this role.

Key Responsibilities
BSc degree in System, Mechanical, Electrical or Biomedical Engineering or related field.
Develop planning of verification activities, ensuring compliance with regulatory standards and company quality objectives.
Developing test methods for test clinical verification and validation.
Develop the test development processes including designs, reviews, implementations, and test execution.
Continuously improving testing methodology, best practices, and standards to provide consistent testing across products.
Work closely with other teams to build and maintain clinical testing.
Work collaboratively with others to drive best practices.

As an Integration System Engineer in the Imaging Technologies team, you will own the end‑to‑end integration of a multidisciplinary medical device, from early design through validation and release.

You will lead system-level bring-up, define and execute integration strategies, and ensure robust interaction between mechanics, electronics, optics, and software.

This role emphasizes hands-on integration, performance analysis, and cross-functional alignment to deliver a high-quality, production-ready scanner.


Key Responsibilities

System Integration Ownership
Own system integration across all subsystems (mechanics, electronics, optics, software) and ensure a stable, testable, and scalable product.
Lead system bring-up, integration flows, and configuration management across development stages.
Identify interface gaps, define integration requirements, and drive closure with relevant teams.

Performance & Testing
Design and execute system-level experiments to evaluate performance, stability, and reliability.
Develop tools and automation for data collection, analysis, and debugging.
Define integration and verification test strategies, including acceptance criteria and coverage.

Problem Solving & Debug
Lead root-cause analysis of complex cross-domain issues.(HW/FW/SW/optics interactions).
Drive containment, corrective actions, and long-term fixes.
Ensure issues are resolved with clear documentation and learning capture.

Cross-Functional Leadership
Work closely with R&D disciplines, QA/RA, and manufacturing to align on system behavior and requirements.
Translate system-level needs into actionable specifications and integration plans.
Act as the technical focal point for integration-related decisions and trade-offs.

Process & Methodology
Establish and improve integration processes, methodologies, and best practices.
Introduce new tools, capabilities, and approaches to increase integration efficiency and quality.
Ensure proper documentation of integration flows, configurations, and test results.

Team Leadership & Mentorship
Mentor junior engineers and guide student contributors.
Assign and review tasks with a strong focus on quality, rigor, and engineering discipline.

We are seeking a highly motivated and experienced Production and Suppliers 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 qualifications and control of ATE testers in V&V phase and production lines.

Support ECO/ECR processes, NPI projects, product updates, and cross-functional engineering changes.

Participate in supplier selection and conduct suppliers audits.

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).

Support RMA/DOA processes and continuous reduction of field failures.

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.

The Project Manager - Global Lumina Scanner Engineering Department is accountable for leading, coordinating, and executing cross‑functional engineering projects across the full product lifecycle, including NPI, sustaining engineering, production support, test infrastructure, and continuous improvement.
The role ensures alignment between Engineering, Operations, R&D, Quality, and Supply Chain, enabling predictable execution, clear ownership, and end‑to‑end visibility of all engineering initiatives.

Key Responsibilities
Lead and manage multiple engineering projects in parallel across NPI, sustaining, test, electronics, and system engineering.
Build and maintain integrated project plans, milestones, dependencies, and critical paths.
Drive execution through all project phases - definition, planning, execution, validation, and closure.
Coordinate design transfer, manufacturing readiness, validations, and GA milestones.
Own project governance: status reviews, KPIs, risk management, escalation, and decision tracking.
Drive cross‑functional alignment between R&D, Manufacturing, Test, Quality, Supply Chain, IT, and Program Management.
Manage ECO‑driven projects and ensure full impact analysis, execution, and closure.
Support supplier‑related projects including readiness, FAIs, tooling, and ramp‑up activities.
Establish clear ownership, priorities, and communication cadence across all stakeholders.
Provide consolidated, real‑time visibility of project status to management.

We are looking for a system engineer to join our talented system engineering department.
As a system engineer you will be leading complex, multidisciplinary projects as a the technical owner, processing the customer needs and values into system specifications and requirements, overview the development and chair the acceptance processes.
Responsibilities
Customer Liaison.
Analysis of customer needs and requirements.
Identification of internal Projects Specifications and requirements.
Ability to lead and manage sub-contractors, including contractual engagements and procurement supervision.
Ability to lead a team of engineers, including the management of work plans and delivery schedules.
Ability to create effective and deployable solutions to complex engineering challenges.
Preparing, Leading and participating in Design Reviews and contractual engagements activities.
Leading acceptance and delivery processes with multiple entities, domestically and abroad.