דרושים בתחום פיזיקה

Be a significant part of the Physical Design team, developing the Designs of the next generation state-of-the-art chips.
Investigate, develop, innovate and improve challenging Physical Design flows.
Multi-disciplinary, Participating in many steps of the Physical Design flow. Escorting the design from RTL to GDS.
Supporting other team's activities which are Physical Design oriented.

 BSc in Electrical/Computer Engineering.
More than 4 years of experience as Physical Design engineer.
Experience in Synthesis and Implementation.
Experience in STA, DFT, DRC, LVS, LEC & Power is advantage.
Experience is Cadence flow is advantage.

· 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

Job description
· Simulation of light matter interaction.
· Learn the program, infrastructure we have.
· Learn our methodology, tool and customer issues.
· Understand specific problems, preform simulation, analyze data, out of the box thinking.
· Summary and presentation.
· Support and drive forward our infrastructure (SW used, servers and methodology)

Job requirements
· MSc/PhD students in experimental physics/applied physics/electrical engineering.
· At least one year remaining till graduation.
· Preferable some experience in the field of laser optics & microscopy.
· Capabilities:
o Strong analytic skills, good problem-solving skills.
o Complex system understanding.
o Designing of experiments.
o Independence & self-driven.
o Innovation & creativity.
· Available for at least 23 hours a week.
· Experience in semiconductor industry – Advantage.