דרושים בתחום הנדסת פיזיקה

Be a member of sales & technical support team
Acts as a direct sales and technical support engineer to customers worldwide
Generate strong relationship with the customers and act as their point of contact
Co-work with the R&D team in order to define solutions to customers,as well as other departments such as purchasing and production.
Meet sales targets

Proven track record of selling complex solutions in the laser/optics fields,OR: experience as an optical design engineer with experience in project management or similar
B.Sc degree or higher in Physics/Engineering
At least 2-3 years of experience in Laser optics – mandatory
Fluent English – speaking, reading and writing
Excellent verbal and written communication skills
Strong business and customer orientation skills
Significant advantages:
Optical design skills
Knowledge of the Laser market
Understanding of electro-optical systems

· B.Sc. in Electro-optics engineering/Physics/Electrical engineering. M.Sc. - advantage
· At least 2 years of relevant experience in the Electro-Optics industry.
· Zemax/Oslo–mandatory, Matlab-mandatory, C/C#-advantage
· Excellent communication skills in both Hebrew and English (speaking, reading and writing).
· Attention to details, conscientious, thorough
· Advantage:
· Experience in lasers/laser optics
· Experience with optical setups, building a setup on an optical bench

• Analysis of needs and alternative solution selection
• Support machine vision application in customers site (including traveling)
• Manipulation and adjustment of image processing algorithm solutions to specific applications
• Develop in house algorithms for machine vision
• Closely work with other development departments in scram teams
• Work with vendors and outside suppliers

• Experience in Multi-disciplinary machines, and machine vision – advantage
• Prior experience in MATLAB is must, Python or open CV advantage
• Prior knowledge in optics and image processing algorithms
• Working in a matrix environment: collaboration with R&D functions
• Strong troubleshooting and problem-solving capabilities.
• Strong technical skills, Execution capabilities, System view, Collaborative, Process oriented

· Develop detailed specifications, construction of prototypes for current and new products.
· Manage requirements, interface specifications, systems models and tests relative to development milestones and help define and refine Systems Engineering & Design Control processes and practices
· Work closely with engineering teams to plan / de-risk remaining development work, taking into account key interactions and interfaces
· Serve as key interface point with external development partners
· Contribute to design and define product testing plans and protocols. Perform testing, analyze results, suggest recommendations and/or conclusions and document clearly and completely in technical reports.
· Ensure that product documentation is in accordance with Quality System requirements design control, quality, and company regulations and national and international regulatory body requirements.
· Maintain and manage activities towards the overall project schedule, and ensure that critical timelines are established and met.
· Ensure that new products are designed to facilitate manufacturability.

· BS/MS in Biomedical, Electrical, Mechanical Engineering, physics or Systems Engineering
· Minimum 10 years overall engineering experience in an interdisciplinary product development environment
· 5 years of this experience in a SE role while operating under a registered QS and the FDA QSR
· Demonstrated competency in program planning, e.g. developing work breakdown structures, resource planning, program risk management
· Thorough understanding of and leading requirements management; from development through verification and validation; experience with requirements management tools
· Thorough understanding and working knowledge of ISO 14971:2007; experience in leading safety risk management activities, e.g. Hazard Analyses, FTA, and FMEA
· Experience in leading the development of product/system architectures
· Thorough understanding of safety compliance process (product safety marks)
· Experience in conduct and support of device clinical trials
· Familiarity of applicable EU New Approach Directives, e.g. MDD, IVDD
· Familiarity of regulatory submissions, e.g. FDA 510(k), CE Marking
· Working knowledge of available industry reference resources, e.g. AAMI, RAPS, INCOSE

· Develop detailed specifications, construction of prototypes for current and new products.
· Manage requirements, interface specifications, systems models and tests relative to development milestones and help define and refine Systems Engineering & Design Control processes and practices
· Work closely with engineering teams to plan / de-risk remaining development work, taking into account key interactions and interfaces
· Serve as key interface point with external development partners
· Contribute to design and define product testing plans and protocols. Perform testing, analyze results, suggest recommendations and/or conclusions and document clearly and completely in technical reports.
· Ensure that product documentation is in accordance with Quality System requirements design control, quality, and company regulations and national and international regulatory body requirements.
· Maintain and manage activities towards the overall project schedule, and ensure that critical timelines are established and met.
· Ensure that new products are designed to facilitate manufacturability.

· BS/MS in Biomedical, Electrical, Mechanical Engineering, physics or Systems Engineering
· Minimum 10 years overall engineering experience in an interdisciplinary product development environment
· 5 years of this experience in a SE role while operating under a registered QS and the FDA QSR
· Demonstrated competency in program planning, e.g. developing work breakdown structures, resource planning, program risk management
· Thorough understanding of and leading requirements management; from development through verification and validation; experience with requirements management tools
· Thorough understanding and working knowledge of ISO 14971:2007; experience in leading safety risk management activities, e.g. Hazard Analyses, FTA, and FMEA
· Experience in leading the development of product/system architectures
· Thorough understanding of safety compliance process (product safety marks)
· Experience in conduct and support of device clinical trials
· Familiarity of applicable EU New Approach Directives, e.g. MDD, IVDD
· Familiarity of regulatory submissions, e.g. FDA 510(k), CE Marking
· Working knowledge of available industry reference resources, e.g. AAMI, RAPS, INCOSE

· Service products development - Develop Service products for multi-disciplinary systems at customer sites based on customers’ needs.
· NPI PLC ownership for Service - Represent the field and service organization during new Products developments , make sure that new systems developments meet service criteria.

· B.Sc. degree in Electrical / Mechanical / Chemical Engineering, physics or a related discipline.
· Required: FAB experience.
· Multidisciplinary approach, system understanding.
· Ability to lead and drive the development process across the organization.