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Sustain Mechanical Engineer
Key Responsibilities:
Full technical ownership of assigned product lines throughout their lifecycle, serving as the senior engineering authority for sustaining activities
Lead mechanical design changes in existing multidisciplinary products to improve quality, reliability, serviceability, manufacturability, and customer experience
Drive cost-reduction initiatives (VAVE / Cost Down) through redesign of mechanical and electromechanical assemblies, materials, and manufacturing processes.
Lead and execute root cause analysis (RCA) for field failures and production issues, defining and implementing effective corrective and preventive actions (CAPA)
Provide ongoing engineering support to manufacturing lines and service organizations, including hands-on troubleshooting and design optimization.
Design and develop jigs, fixtures, test equipment, and manufacturing tools for assembly lines and validation processes
Manage engineering changes with global suppliers and contract manufacturers, including plastics, injection molds, CNC machining, sheet metal, piping, and turnkey electromechanical assemblies
Lead First Article Inspection (FAI) processes for new parts, tools, and suppliers, including qualification and approval activities

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.

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.

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 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.