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We are looking for an experienced software & algorithm engineer to join our computational drug hunting team.
Responsibilities:
Design and build a scalable, complex backend infrastructure for our computational cloud platform
Advocate lean and mean solutions, aesthetic design, and architecture
Implement and improve algorithms in our bioinformatic pipelines
Conduct literature reviews for algorithms, bioinformatics methods and big data solutions, and continuously keep up to date with the state of the art
Help define the technological strategy of the company

we are looking for a motivated and skilled validation engineer to join our exciting project.

In this role, you will have a direct impact on our product. As a team member, you will be responsible for the operating and maintaining a world wide automation testing system, analyze and debug the testing results and report results and issues into data systems.

The project you will be working on is a total solution (edge to cloud) of unique B2B internet of things (IoT) service.

If you are passionate about working with cutting edge technologies and willing to join our growing team, we want to meet you!
Responsibilities
Verify functional and performance features of Sony products.

Operate and maintain automation testing setups world wide.

Design, implement, maintain, and run automation campaigns on various setups on weekly/monthly basis.

Analyze and debug test results and report results and issues into data systems.

We are seeking great talent to help us build The DNA of tech.
Our company manufactures one of the worlds largest portfolios of discrete semiconductors and passive electronic components that are essential to innovative designs in the automotive, industrial, computing, consumer, telecommunications, military, aerospace, and medical markets.
We help the worlds most in-demand technologies come to life.
Every day our products touch your life and the lives of people across the world.
Come join us and help us build The DNA of tech.
Our company is a Fortune 1,000 Company listed on the NYSE (VSH).
Our company in Dimona is currently seeking applicants for a Process Engineer.
You will be responsible for designing, evaluating, and optimizing production processes to improve efficiency, reduce waste and cost, and ensure product quality.
Our company provides its employees with support, a variety of tools for personal growth and a wide range of opportunities and advanced career within the company.
Our company is a stable and solid company which has served as home and family to thousands of its employees for many years.
What you will be doing:
Develop and implement production processes in line with product specifications and quality standards.
Identify and analyze process issues and recommend improvements to increase efficiency and reduce waste.
Create and maintain production documentation, such as standard operating procedures and work instructions.
Collaborate with other departments, such as Manufacturing, Quality Assurance, and Research and Development, to ensure smooth production processes.
Monitor and evaluate production processes to identify opportunities for improvement and implement solutions.
Train and mentor production and maintenance teams on new processes and equipment.
What can we offer you for your talent:
Our company offers a comprehensive suite of benefit programs and other resources designed to help you achieve your personal and professional goals.
With us, youll experience unique career paths, an open and collaborative culture, a stable business that will be there for you, and opportunities to work globally and locally.

We are looking for experienced, creative and impact-oriented Algorithm Developers to join our team!

As an Algorithm Developer you will be responsible for building the algorithms powering our platform and our consumer applications (Wordtune Suite). You will be part of a multi-disciplinary team that also includes engineers and product professionals, all working together to bring our products to life.

You will take part in the full life cycle of our development process, deeply understand the problem we are solving, come up with algorithmic approaches for solving these problems, devise strategies for collecting necessary training data, train and evaluate large language models and other machine learning models and also be in charge of deploying these solutions in production.

ROLE AND RESPONSIBILITIES
Build the algorithms that power our various products
Develop production-grade solutions to challenging product-driven NLP tasks by combining deep language models, classical ML/NLP and algorithms
Collaborate with product, sales and customer success teams to define success criteria and translate them into quantitative measures and objectives
Devise innovative strategies for collecting training and evaluation data
Train and evaluate models in realistic production scenarios
End-to-end ownership of the algorithmic components of our products, from design, through implementation and monitoring in production

A Global medical high-tech Company located in Shoham, is seeking a Quality Assurance and Regulatory Affairs Specialist with experience managing the development of medical devices through the approval process. The ideal candidate will have a strong regulatory and quality knowledge throughout product lifecycle with aspects of effective management and strategy.
Responsibilities & Scope of work:
Supports and maintains EU- MDR submission related activities (QMS, Technical Files, GSPR and PMS) and liaises with regulatory authorities
* Participation in internal and external audits e.g., FDA, Notified Body etc. for regulatory affairs matters - Oversight and performance of routine QA activities such as: ECO, MRB, NC, Monitoring of Calibrations, Training and Qualification, Customer Complaints, CAPA, Document and Record Control, Approval of qualification and validation activities etc.
* Control of processes in compliance with the applicable regulations and company procedure requirements - Participate in Management Reviews and analyze quality data
* Work closely with R&D through product development process and design activities.
* Support risk management activities including hazard analysis and FMEA. - Provide technical review of data or reports that will be incorporated into regulatory submissions to assure scientific rigor, accuracy, and clarity of presentation.
* Identify relevant guidance documents, international standards, or consensus standards and provide interpretive assistance.
* Maintain current knowledge base of existing and emerging regulations, standards, or guidance documents including the Medical Device Regulation (MDR), and all other standards/regulations included within applicable scope.
* Support and improve company Quality Systems by creating a quality culture and provide ongoing education on compliance activities.
* Contribute towards accomplishment of departmental and corporate goals and objectives
* All other duties as requested by his/her manager.

Required Analyst
Job Description:
A clinical-stage drug discovery and development company in the field of cancer immunotherapy. In line with our business model to enter into collaborations for their internally discovered, novel therapeutic candidates at various stages in research and development, the company is seeking an Analyst in support of its partnering efforts.
Reporting to the SVP Strategic Collaborations, the Analyst will lead competitive intelligence (CI) and business analysis activities to support BD and corporate objectives. She/he will be responsible for supporting aspects of competitive analysis and other activities relating to partnering efforts.
Constantly monitor the pharma and biotech space and gather competitive intelligence from various sources including company portfolios, preclinical and clinical activities, scientific data, partnerships, deal structures and terms, and other relevant intelligence
Perform analyses and provide insights into competitive landscapes, industry trends and perspectives, market developments, product developments and positioning, as well as other intelligence in support of our BD&L and R&D efforts
Provide regular updates to our management and functions
Develop Target Product Profiles for our development candidates in close collaboration with R&D teams, and build forecast models based on epidemiological data as well as customer/patient segmentation, pricing and access assumptions
Identify potential collaboration partners for various pipeline opportunities
Work closely with our R&D community and drive the preparation of materials surrounding the companys pipeline programs for internal presentation to management and also to potential partners
Contribute to the creation of valuation models and financial valuation of business development opportunities against partnering scenarios.

Required Research Lab Technician
Job Description:
The research technician will support ex-vivo and in-vitro experiments, as a part of the functional validation of immunomodulatory molecules discovered by us.
The research work under the supervision of scientists will include expression studies in human and mouse tumor-infiltrating immune cells, and functional immune assays for elucidation of mode of action.
Assist in processing and characterizing human and mouse tumor tissues
Perform immune cell isolation from human and mouse blood
Support tissue culture experiments (flow cytometry, cytokine analysis)
Assist in genotyping of mouse strains
Support with laboratory maintenance duties e.g., handling routine tasks such as preparing stocks of common lab reagents, maintaining lab databases, etc.
Temporary position until the end of the year 10 hours a week.