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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.

Required Senior Design Verification Engineer ​
Background
Things work differently in space. We develop New-Space hardware and software that work flawlessly in harsh space conditions. Our technology is already deployed in space and used in many satellites and more than 50 space missions across the solar system with zero failures.
We are expanding our Design Verification team, and invite you to explore Space with us! The job includes taking a viable role in the VLSI verification tasks of our line of products.
What you will be doing:
Be part of the verification Team
Plan & implement UVM verification environments
Interact with Architecture, Design, SW and Validation teams
Define new DV methodologies and improve existing ones
Work on both ASIC and FPGA Space system projects.

If you are looking to make an impact, come and join a team developing the next generation of space communication technology. We are looking for an experienced Algorithms Engineer to lead the innovation of the next-generation space connectivity technology.
What you will be doing​:
Design and develop state-of-the-art communication algorithms.
Key contributor to modem and MAC architecture, design, and implementation.
Conduct and lead algorithm research, including theoretical analysis and simulations.
Lead technical reviews with key stakeholders to present algorithms and system design approaches.
Work closely with System, RF, HW, SW teams to lead high-impact technical decisions about system design and implementation.

We are looking for an Algorithms Manager who will lead the design and implementation of the automotive imaging radar Algorithms stack.
What will you do?
Lead the team which defines and scales up our radar high performance algorithms and make them meet the ADAS and Autonomous Vehicles standards and beyond
Drive and consistently improve our radar performance
Identify key areas of Next Generation improvements, recommend research directions and system solutions
Design, develop and implement Radar data analysis methodology
Be a knowledge source for automotive radar KPIs
Work closely with different stakeholders that include external customers and internal interfaces like SW, HW, and others.

We are looking for an Algorithms Engineer who will handle the design and implementation of the automotive imaging radar Algorithms stack.
What will you do?
Be part of the team that defines and scales up our radar high performance algorithms and make them meet the ADAS and Autonomous Vehicles standards and beyond
Consistently improve our radar performance
Design, develop and implement Radar data analysis methodology
Be a knowledge source for automotive radar KPIs
Work closely with different stakeholders that include external customers and internal interfaces like SW, HW, and others.

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.