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Provide our customers technical and engineering expertise in their ASIC design HW verification process, using our HAV Platforms and Solutions:
Analyze customers verification methodologies and targets, platform and Testbench solutions planning.
Drive and execute HAV products Evaluations on customers designs.
Support customers in deployment of the HAV products, from RTL code compilation and synthesis, towards SoC-level full functionality bring-up on the systems.
Hands-on bring-up of Emulation Testbenches, including interface protocol Transactors, memory models SpeedAdapters, C++ code, and automation scripts.
Regularly interact with customers as their first contact to address any quality issue or required improvements in our products and their collaterals.
Work internally with R&Ds to provide feedbacks on products, track development process and roadmaps.
Work internally with Sales team on accounts strategy and business growth opportunities.

We are looking for a Senior Chip Design Verification Engineer for developing the next generation DFT technologies.

As a Senior Chip Design Verification Engineer in the DFT team in our coompany, you will verify the design and implementation of our DFT technologies in various projects. This position offers the opportunity to have real impact in a dynamic, technology-focused company impacting Switches, Nic and SoC product lines. We are working closely with a wide range of aspects - chip design, backend, verification and production testing. We are working on the most advanced technologies and complex products. Our DFT solutions are unique, innovative, and we are continuously looking for new and creative solutions to meet the challenging goals.

What you'll be doing:
In this position, you will be responsible for verification of the DFT design, architecture and micro-architecture using sophisticated verification methodologies.
As a member of our DFT verification team, you'll understand the design & implementation, define the verification scope, develop the verification infrastructure (Testbenches, BFMs, Checkers, Monitors), execute test/coverage plans, and verify the correctness of the design.
Collaborate with architects, designers, emulation, production testing and silicon verification teams to accomplish your tasks.

We are looking for a skilled and driven Experiment Operator to join our team.
As an Experiment Operator, your role will be examining and interpreting extensive datasets in order to derive valuable insights and offer actionable solutions.
You will have the opportunity to work both independently and collaboratively in a variety of testing environments, such as laboratories and outdoor settings.
It is expected that you display proficiency in operating multiple devices efficiently.
Additionally, your contribution will be valuable in creating test plans and reports to effectively manage and organize test data.

We are looking for outstanding Algorithms Developers to join our team.
In this role, you will do:
End to end development and deployment of high frequency trading algorithms.
Development and application of trading algos in a highly competitive real time environment.
Analyzing large and complex data sets finding ways to improve existing trading strategies.
Building scalable infrastructures and developing algorithms for modeling the financial market.

Required ASIC Verification Engineer
Verification Group in a growing group responsible for pre-silicon ASIC Verification of complex chips implementing an advanced modem technology.
As part of the role, you will architect, develop & own blocks / sub-subsystem / system-level verification benches. You will be a major contributor to advanced SV UVM methodologies and to infrastructure development. You will be part of an advanced development flow, using state-of-the-art development & Verification tools and will work closely with the chip architects and RTL / VLSI design teams.
RESPONSIBILITIES
The Verification Engineer will be responsible for different HW blocks at module-level and sub-system level and is expected to:
Have an expert-level understanding of assigned HW blocks as well as a good understanding of the block in the context of whole system.
Communicate with architect, designer, algorithm and other verification engineers to lead complex verification tasks, both on module-level and sub-system testing.
Design complete verification environments.
Implement design in full UVM environment.
Perform full block regressions and collection of functional coverage.

Required Algo Engineer
Within the Algorithm team, you will be responsible for designing and specifying new architectures/algorithms for the physical layer of wireless products. You will work tightly with SW team, ASIC team and Integration team.
RESPONSIBILITIES
Design new algorithms/defining new architectures for the existing and future products
Implement and validate the methods in the baseband simulator of the DSP team
Produce and update design/performance documents along with the development process
Support of the Asic team for the Verilog/VHDL implementation
Support for investigations on performance issues in house and on site.

Were looking for innovators with the passion, creativity, and drive to help us take on new challenges and deliver real results for our customers. AI/ML team lead will actually lead the design and development of the companys main product.

We are currently seeking a Python Game Designer.
What You'll Do
Conducting in-depth mathematical creation and setting of online real money games, focusing on probability, statistics, game mechanics, features, and theory.

Calculating and optimizing online real money game probabilities, odds, and payouts, considering random number generation and statistical distributions.

Refining mathematical models that govern the mechanics and outcomes of various online real money games.

Collaborating closely with game product management, designers, developers, and stakeholders.

We're looking for a sharp and passionate Business / Product Data Analyst to join us to the product team.
Using your technical and analytical skills, you'll be responsible for telling the story behind the numbers, to understand how users interact with our products, and provide insight regarding new ideas to implement.
Responsibilities:
Be on the cutting edge of analysis, leveraging our data sources to propose new ideas that youll then see implemented.
Analyze large data sets representing users behavior, see beyond numbers and help to inform, influence, support and execute our business and product decisions.
Plan and analyze effective A/B tests in order to improve business KPIs.
Build reports and dashboards to monitor product performance, key business metrics and user experience.

We are looking for a Clinical and RA associate.
Primary function of the position:
Under the oversight of the CRA manager (CTM) the person ensures compliance of study conduct with ICH/GCP and country regulations, companys policies and procedures, quality standards and adverse event reporting requirements internally and externally.
Acts as primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility of allocated sites.
Roles and responsibilities:
Develops strong site relationships and ensures continuity of site relationships through all phases of the trial.
Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs, Local Laws & Regulations, Protocol, Site Monitoring Plan and associated documents.
Gains an in-depth understanding of the study protocol and related procedures.
Coordinates & manages various tasks in collaboration with other sponsor roles to achieve Site Ready.
Performs remote and on-site monitoring & oversight activities using various tools to ensure:
Data generated at site are complete, accurate and unbiased
Subjects right, safety and well-being are protected
Conducts site visits including but not limited to initiation visits, monitoring visits, close-out visits and records clear, comprehensive and accurate visit & non-visit contact reports appropriately in a timely manner.
Collects, reviews, and monitors required regulatory documentation for study start-up, study maintenance and study close-out.
Communicates with Investigators and site staff on issues related to protocol conduct, recruitment, retention, protocol deviations, regulatory documentation, site audits/inspections and overall site performance.
Supports and/or leads audit/inspection activities as needed
Following the country strategy defined by CRD and CTM, contributes to the identification of new potential sites and works closely with them to develop strong clinical research capabilities
Whiling to travel abroad including US for sites oversights

Were looking for a brilliant and ambitious Data Scientist who is seeking his next challenge, with proven experience in big-data analysis, machine learning algorithms and digital signal processing.
We invite you to work in a creativity oriented, vibrant and non-formal environment that will encourage you to learn, grow your research and development skills and experience while executing end-to-end algorithm development process of a unique platform aim to improve patients quality of life and survival.
Job description:
Execute statistical modeling and analysis of large data sets using ML and big-data algorithms
Perform end-to-end research and development of speech signal processing algorithms

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.