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We are seeking a process and mechanical engineer to join our dynamic Test Engineering team. As a key member you will be responsible for solving production failures, increase our yields, reduce MRB and initiate cost reduction activities, design tools, fixtures, and jigs to support robust manufacturing of products.
The production engineer will have a full ownership over the testers in the production line, including a full understanding of their processes, products and BOMs to ensure a high yield with a high-quality product.
Key Responsibilities:
Define and design jigs, tools and fixture to allow repetitive and robust manufacturing with mass production orientation.
Lead investigations and find solutions to improve manufacturing yield and product quality
Work on production line escalations to resolve short and long-time issues.
Leading Engineering changes as the prime interface to introduce necessary engineering/R&D changes while understanding the implications in Logistic, Testing and Production.
Have knowledge and involvement in all disciplines (Electronics, Mechanics, and Optics) and attendance in production to improve Production processes.
Construct and maintain complex Bills of Materials (BOM).
ECOs Leading and writing DVP/IOQ/PQP protocols and reports for change validations at production line.
Work closely with other disciplines in the organization to coordinate various activities such as purchasing, R&D, Quality, Planning, Production etc.
Conduct risk assessments and implement mitigation strategies to minimize integration challenges.

we are looking for a Project Manager.
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 seeking a highly motivated and experienced Sr. Production and 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 RMA/DOA processes and continuous reduction of field failures.
Support qualifications and control of ATE testers in production lines.
Support ECO/ECR processes, NPI projects, product updates, and cross-functional engineering changes.
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).
Participate in supplier selection and conduct suppliers audits.
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.

we are looking for a Verification and Validation Engineer.
Daily duties include reviewing business and technical specifications to write and execute automated and manual test scripts for quality assurance testing.
The candidate will be responsible of defining test strategy, execute test plans, review tests product specifications and participate in defining/selecting appropriate test tools and automation strategy.
This function will work closely with HW Development, Program Management, and Operations team to test and roll out the releases.
Key Responsibilities:
You will be required to support a variety of corporate business applications and web based products in a QA environment.
Handle and support dynamic schedule, multiple environments, test cycles and deployments.
Responsible for verification and validation tests plans with the ability to maintain and cross-reference it with risk analysis matrix
Develop and maintain test methods, equipment and instruments for medical device throughout all development and production stages of the product
Performing validation and testing of hardware (mechanical, electronic implantable devices) and SW for prototypes and products.
Leading projects to develop and coordinate testing procedures for prototypes and products
Design, selection and documentation of test equipment (HW).
Formulates test guidelines, Acceptance Tests procedures, protocols, and tests reports.
Responsible for specification, purchasing and maintenance of laboratory test equipment.
Participate and lead engineers in designing features and requirements
Introduce the team to new technologies relevant to their current challenges and to the future challenges of the product.