לוח משרות דרושים כימאי

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.

Power the Future with us! SolarEdge (NASDAQ: SEDG), is a global leader in high-performance smart energy technology, with over 5000 employees, offices in 34 countries, and millions of products installed in over 133 countries. Our diverse product offering comprises intelligent solar inverters, battery storage, backup systems, EV charging, and complete home energy management ecosystems. By leveraging world-class engineering capabilities and with a relentless focus on innovation, we strive to create a world where clean, green energy from the sun is the primary source of power for our homes, businesses, and just about everywhere we thrive As a Battery Certification Expert, you will be responsible for ensuring that batteries/Storage systems comply with regulatory standards and industry certifications. Your role involves overseeing the certification process for battery products, collaborating with regulatory bodies, and providing guidance to internal teams on compliance requirements. You will stay updated on evolving regulations and standards related to battery technology, ensuring that products meet all necessary criteria for safety and performance. You will participate and influence standards and regulations drafting in international standardization committees by forming alliances with the industry’s leading authorities and competitors. Additionally, you will work closely with engineers and product managers to address any compliance issues and facilitate the successful certification of battery products. .You will indirectly manage activities across multiple teams including R&D and Product management. What will you be doing:
* Manage the end-to-end certification process for battery products, including planning, documentation preparation, testing, submission, and communication with certification agencies.
* Stay informed about global regulations, standards, and certification requirements applicable to battery technology.
* Participating in International Standardization committees to influence current and future industry’s standards to provide advantage to SolarEdge’s products.
* Internal Guidance: Provide guidance and support to internal teams (engineering, product management, quality assurance) on compliance requirements, testing methodologies, and documentation needed for certification.
* Quickly learn and solve unfamiliar customer technical & commercial issues caused by local regulation laws.
* Identifies and recommends compliance with standards that apply to the company’s current and future products. Standards analysis includes periodic review of coverage by technical area, by relevance and by geographic market.
* Interacts with third party accredited compliance verification entities to ensure Engineering and Product Verification have accurate interpretation of standards clauses.

Country:
Israel

City:
Herzliya

* 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

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.

At our company, we love meat. Really, really love meat.
We believe that the world deserves plant-based meat, thats not only good for the environment but is also kind to animals.
Having studied animal meats unique components, and perfected cutting-edge technologies, our company provides a wide range of high-quality products that are just as delicious as the meat you already know and love. Our company delivers an uncompromised and extraordinary culinary experience with its taste, texture, and aroma.
We also know that we will reach the unreachable with a great team of passionate, courageous, and curious people.
Were as passionate about people as we are about food!
Your challenge:
Troubleshooting lab analyses and equipment.
Maintaining the site Food Safety program.
Manage ingredient and packaging storeroom and responsible for maintaining inventories of ingredients, packaging, and supplies.
Responsible for ordering the ingredients for the lab and managing the connection with the lab suppliers.
Develop and utilize an automated system for inventory management.
Manage ordering and receiving ingredient, packaging, products.
Manage all shipping and receiving activities as requested by R&D team.
Location- Rehovot.

Our company is seeking an International Business Development Manager to join our team in Haifa.
The Business Development Manager will report to the VP of Sales & Marketing.
RESPONSIBILITIES:
Responsible for defining the sales strategy of the Companys products and its implementation in the territory chosen.
Define the price policy in accordance with the strategy set with VP for sales & marketing.
Responsible for managing the sales activity of agents and distributors in the territory granted to him.
Responsible for locating and developing new markets/customers and setting product development goals /and applications.
Annual contracts and visits to customers and coordination.
Participation in exhibitions around the world.
Frequent travel for customer meetings and market development.
Building an annual budget for his/her territory.
Competition analysis.