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At our company Yokneam, we are driving innovation in gastrointestinal diagnostics, transforming patient care with minimally invasive solutions. Our multidisciplinary teams in R&D, engineering, manufacturing, and quality work together to develop, produce, and deliver cutting-edge medical devices that improve patient outcomes worldwide. We are seeking a Manufacturing Engineering Manager to lead engineering initiatives, optimize production processes, and ensure high-quality, efficient manufacturing of our next-generation GI diagnostic technologies. This role offers the opportunity to make a significant impact on global healthcare while working in a collaborative, innovative environment.
Responsibilities may include the following and other duties may be assigned:
Plans, directs, and implements all aspects of the company's site engineering activities (safety, manufacturing process performance, testers development and implementations, product configuration, PMO, validation aspects, etc).
Develop, evaluate, implement, and maintain technical quality assurance and control systems or reliability systems and standards pertaining to materials, techniques, or company products.
Oversees the investigation and evaluation of existing technologies, testers development and implementation in production process.
Monitors documentation maintenance throughout all phases of product lifecycle.
Selects, develops, and evaluates personnel to ensure the efficient operation of the function, driving performance and increasing people engagement.
Drives a continuous improvement mindset in Engineering by engraining and improving the MPS (our company Performance System) methodologies in the day-to-day.
Has budget accountability for the department including CAPEX investment plan.
Meets deadlines on critical projects & Actions committed by Site Eng Org (CAPA / PMO Projects / EHS / Local Projects)
Ensures that quality tools such as CAPA / FMEA are understood and used by Site Eng department
Improves Yokneam Operations KPIs (Yields, OEE, Savings).
Improves manufacturing availability means (OEE, up-time, Productivity)
Controls and improve process and product performance (RTY, Scrap reduction)
Reduces cost and improve productivity (Costs, Programmatic Savings)
Leads and coordinates product quality investigations. Acts as a key partner on investigating root causes

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.
In this role, you will
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.

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.

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.