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We are looking for experienced Critical Components Engineer to join our outstanding Networking Silicon engineering team, developing the industry's best high speed optical communication devices! Come and be a part of a phenomenal company with an outstanding atmosphere while ensuring our optical products reliability and performance

What you will be doing:

New critical component Qualification and Reliability assessment.

Run DOEs and corners samples analysis to evaluate system level performance.

Set automation tools ,monitors and screening methodologies to control critical components introduction to the manufacturing line.

Investigation of reliability issues at the CM and Customers sites.

We have been transforming computer graphics, PC gaming, and accelerated computing for more than 25 years. Its a unique legacy of innovation thats fueled by great technologyand amazing people.

Today, were tapping into the unlimited potential of AI to define the next era of computing. An era in which our GPU acts as the brains of computers, robots, and self-driving cars that can understand the world. Doing whats never been done before takes vision, innovation, and the worlds best talent. Youll be immersed in a diverse, supportive environment where everyone is inspired to do their best work. Come join the team and see how you can make a lasting impact on the world.

What youll be doing:

Provide PCB Technology support to the Networking BU Engineering Teams; and also, to Signal Integrity, PCB Design, PCB Sourcing, and OPS Engineering.

Develop close relationships the PCB Supply Base and Material Laminate Suppliers applicable to NBU PCB designs.

Help establish and build optimize PCB stack-ups to improve reliability and with cost avoidance concepts.

Resolve NBU PCB Supplier issues, corrective actions, and prevent issues from reoccurring.

Lead the development of PCB Technology and Material Roadmaps established from NBU Engineering needs and for next generation products.

Own the efforts with all Suppliers such that they are capable and ready to meet the NBU PCB Roadmap requirements; and qualify Suppliers with new technologies and materials.

Lead the Research & Development of new PCB Technologies, Interconnect Structures, and Materials required for new Products, Product performance improvements, and cost reductions prior to the time needed by NBU Engineering.

Frequently communicate and update NBU PCB and Supplier activities with the PCB Team in Santa Clara.

For a company specializing in the development and production of machines and saws for cutting silicon and hard materials in the field of microelectronic components
Location: near Yokneam
looking for you
General Job Description : Working to develop & support new and existing products Department: Engineering & R&D Blades Reporting: Engineering & R&D Manager
Responsibilities:
• Optimize the materials, chemical process & procedure • Perform process experiments and optimization • Adapt of new technologies, designs of experiments and new laboratory techniques • Write experimental results and technical reports and present at group and R&D meeting • Record all process information regularly and clearly to allow review and generation of commercial process instructions • Perform application tests with application lab in order to qualify new blade performance • Creating and developing new products to meet market demand • Support and train new staff in all procedures, move R&D to production

We are looking for a Medical writer and Regulatory Affairs associate.
Primary function of the position:
Clinical scientific knowledge and writing skills to effectively and clearly communicate medical science information in writing. Generally, focus on either scientific medical writing, which includes clinical studies, and regulatory documents, scientific articles or marketing medical writing. Experience in regulatory aspects (RA), help to lead regulatory strategy and provide ongoing regulatory input.
Roles and Responsibilities:
Work with clinical teams and clients to understand the nature of the scientific work that they will be covering.
Assess data or products using medical expertise, and quickly develop expertise in new areas as needed for their writing.
Help to write studies for submissions to the FDA. The writing is also used in publications or medical journals, or for internal company use.
Comprehensive writing of clinical study reports, study protocols, annual reports, investigator brochures, risk/benefit analysis and integrated summaries from raw data.
Prepare abstracts, scientific exhibits, posters and verbal presentations.
Help with develop and write pharmaceutical training materials, eLearning content, video scripts, magazine articles, and presentations to be used by a variety of audiences.
Conduct comprehensive literature searches to enhance background understanding, and evaluate and analyze the information which will be written about.
Provide responses to regulatory agencies regarding product information or issues.
Maintain current knowledge of relevant regulations, including proposed and final rules. Help in manage activities such as audits, regulatory agency inspections etc.
Participate in the development or implementation of clinical trial protocols. Preparation and submission of regulatory agency applications, reports, or correspondence.
Provide regulatory guidance to departments or development project teams regarding design, development, evaluation, or marketing of products.