דרושים » הנדסה » Chemist / Chemical Engineer

About the role: Development of new lab and industrial-scale technologies
Responsibilities include:
* Developing innovative formulations for printing, dyeing, and finishing of fabrics and
* fibers.
* Conducting lab research experiments in the area of organic and polymer chemistry.
* Performing characterization of the experimental products using analytical and
* spectroscopy techniques.
* Documentation, analysis, evaluation, and presentation of the experimental results.
* Literature review and summary of the results.

We have been transforming computer graphics, PC gaming, and accelerated computing for more than 25 years. Its a unique legacy of innovation thats fueled by great technologyand amazing people. Come join the team and see how you can make a lasting impact on the world. As an Optical Assembly Process Engineer, you become part of the company`s R&D team, and you will be working on the forefront of the communication technology, building the interconnection infrastructure for the Sophisticated Computing and Artificial Intelligence revolution.

What you'll be doing:

Participate in the process of bringing up a new technology from the R&D stage, to the engineering and bring-up then to the high volume manufacturing lines.

Characterizing and investigating of the compatibility of new adhesives, soldering material, packaging material, etc. , to the optical, interconnect products.

Running both quick and organized experiments related to materials, using dispensing and UV curing tools.

Running scanning electron microscope for many hours.

Help in the debug of failures using various methods inspection and characterization methods.

* Research and development of novel dielectric materials for use in additive manufacturing microfabrication.
* Hands-on resin formulation of novel resins for 3D DLP printing based with acrylates, epoxies, etc.
* Formulation of composite resins with various fillers and additives (application of dispersion techniques).
* Characterization of formulation and functionality (e.g. dispersion quality, curing characteristics, rheology, surface tension)
* Characterization of polymeric materials (e.g. mechanical and thermal properties)
* Close collaboration with process engineering
* Management of health and safety regulations in the laboratory

Group:
Fabrica

We are looking for an experienced computational chemist to join our team.
Responsibilities:
Support drug discovery projects with advanced data analysis and molecular modeling
Work in an interdisciplinary environment, developing and executing computational chemistry strategies to drive problem solving within the project
Apply chemoinformatic methods including structure-based and ligand-based drug design techniques for virtual screening, and lead optimization.
Develop AI/machine learning, statistical modeling and generative design tools for drug discovery.

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.

Lead R&D - Food application. 
We are looking for an experienced, motivated and hardworking experienced senior food technologist/ Scientist with the appropriate background to lead R&D projects for food & oil application.
Responsibilities:
Partaking in all aspects of projects: R&D, process engineering, scale-up to production, regulation, and quality requirements. 
Knowledge of process planning and risk management - an advantage.
Planning, executing and documenting laboratory experiments.
Writing professional documents for clients, subcontractors, and investors.
Coordination of experimental activity with subcontractors and outsourcing services.
Additional requirements:
Private vehicle.
Willing to work excess hours.
The ideal candidate should be detail-oriented, innovative, and have a passion for food and science. They should have the ability to think critically, work independently, and manage multiple projects simultaneously.
Please send CV to our e-mail.

We are looking for Process/ Validation engineer

Location: Yahud

Job Description:

Perform validation including writing work instructions and protocols.
Write validation reports (IQ/OQ), support and implement engineering change orders for products, including receiving customer requirements and translating them into engineering requirements.
Provide engineering support for various projects including production processes and integration, as well as addressing issues and non-conformities.

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.