לוח משרות דרושים ייצור ותעשייה

You will be an integral part of the team that supports the companys quality policy to Put Patients First. This team collaborates with global teams to support products across several portfolios. This is a flexible role where the employee is at a minimum 3 days a week on site in the office with option of remote working for 2 days in the week.
Responsibilities may include the following and other duties may be assigned:
Develops, modifies, applies and maintains quality processes and protocols to support servicing of reusable medical devices
Collaborates with engineering and operations functions to ensure quality requirements are in place and met
Devises and implements methods and procedures for processes related to servicing of medical devices
Supports and/or leads audits and inspections from the auditee perspective for service processes in quality management systems
Ensures that corrective measures meet acceptable reliability standards and that documentation is compliant with requirements.
Supports and/or leads projects to improve compliance or standardize service and repair related processes
R57831

we are looking for a Assembler II.
Responsibilities may include the following and other duties may be assigned.
Performs a variety of tasks ranging from repetitive to non-repetitive production assembly operations.
Works from visual aids, method layouts, diagrams, schematics, process flow sheets and written or verbal assembly instructions.
Sets initial layouts, and uses a variety of tools to prepare product(s).
Makes continuity checks on work in process and completed.
May conduct quality inspections on processing line in accordance with quality specifications.
May disassemble, modify, rework, reassemble, and test experimental or prototype assemblies and subassemblies according to specifications and under simulated conditions.
R57572

Design Quality Engineer is responsible for driving exceptional product quality for the patient safety, customer value beyond expectations, regulatory assurance, and optimized Cost of Quality for the Company. This is a key technical position, affecting part quality for both installed base and NPI products.
Key Responsibilities:
Daily duties include supporting the project team (R&D, SQA, Product, System and so on) during the development of a project. Our engineers review each design input and output deliverable throughout the development process and resolve compliance impediments as they arise. As a senior engineer the candidate will be responsible for defining two major evolving components in our work:
Implementing AI in our processes - What are the regulatory requirements for implementing AI in a medical device and how to implement it in our development lifecycle.
Cybersecurity work instructions in compliance with the new FDA guidance, train the various teams on the guidance and its implications to our process, and establish best practices for supporting post market vigilance.

Join our dynamic warehouse team as an Outgoing Quality Inspector, where you will play a critical role in ensuring product quality and compliance before items leave our facility.
This position is ideal for detail-oriented professionals who take pride in accuracy and maintaining high standards.
You will be part of a fast-paced environment that values precision, teamwork, and continuous improvement.
Key Responsibilities:
Perform final inspections on products and shipments to verify compliance with quality standards and customer specifications.
Check labeling, packaging, and documentation for accuracy before dispatch.
Identify and report any defects, discrepancies, or non-conformities promptly.
Collaborate with warehouse staff and quality teams to resolve issues and maintain workflow efficiency.
Maintain accurate inspection records and ensure proper documentation for audits.
Follow safety protocols and contribute to a clean, organized work environment.
Overseeing the performance of all other global warehouses.
Support continuous improvement initiatives by providing feedback on recurring issues.

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 seeking a highly motivated and detail-oriented Production and Supplier Quality Team Leader . This role is responsible for ensuring the
highest quality standards in production and supplier-provided components, driving continuous improvement, and maintaining compliance with
medical industry regulations.
In this role, you will
Lead and manage the Production & Supplier Quality team.
Develop and implement quality control processes for materials and products.
Collaborate with suppliers on quality agreements, audits, and corrective actions.
Oversee incoming inspections and ensure compliance with ISO 13485, FDA, MDR.
Drive continuous improvement using Six Sigma, Lean, RCA.
Conduct internal/external audits and manage CAPA, NCR, and risk documentation.
Mentor team members and foster a culture of quality excellence.

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 Sr. NPI Technical leader.
The Sr NPI Engineer will be responsible to represent the Operation and lead new projects and transfer them to production including the following:
E2E OPS rep for all New Products Introduction cross functional, following PLCM.
Responsible for building Product/Production file, Product documentation, BOM, jigs/tools/Fixtures design
Manage TK vendors and Critical vendors
Responsible for moving from prototype to mass production, including PL establishment and manufacturing strategy
Responsible of full Design transfer process during the PLC stages.
Full cooperation under Program and Project managers guidance

We are looking for an experienced Opto-Mechanical Designer to join our R&D team. You will be part of the design and development of opto-mechanical systems, with a focus on medical device development.
With a strong background in mechanical engineering and experience in opto-mechanical design, you will contribute to the creation of cutting-edge medical devices that positively impact dental healthcare worldwide.
Key Responsibilities:
Design and develop and integrate opto-mechanical systems for medical dental devices.
Collaborate with cross-functional teams on multidisciplinary systems.
Utilize CAD software (SolidWorks is advantage) to create detailed designs, prototypes, and engineering drawings.Design and execute tests across multiple disciplines and methodologies.
Conduct feasibility studies, risk assessments, and performance evaluations for opto-mechanical systems.