לוח משרות דרושים מדעי החיים, טבע וחקלאות משרה מלאה

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.

We are seeking an experienced antibody Scientist to facilitate our R&D efforts. As a key member of our multidisciplinary team, you will drive the discovery, design, and optimization of novel immunotherapy modalities using state-of-the-art computational, structural and biological methods.
Key Responsibilities:
* Implement cutting-edge structural methods, including molecular dynamics simulations, homology modelling and docking studies, to design antibody drug candidates.
* Harness AI/ML approaches and Antibody/Protein Engineering techniques to discover and optimize therapeutic antibodies.
* Stay updated with emerging technologies in structural biology and integrate novel approaches into our research programs to maintain our competitive edge.
* Appley molecular biology tools (Yeast display, Tissue culture, Flow cytometry, FPLC, HPLC, AKTA, ELISA, etc.) to produce and TEST antibodies in the lab.
* Collaborate closely with other laboratory personnel and CROs (Contract Research Organizations) to oversee antibody production, quality control, and efficacy testing.
* Contribute to project planning, scheduling, and cost estimation, ensuring timely and cost-effective delivery of assigned projects.
* Foster a culture of collaboration and excellence by building effective working relationships with colleagues, management, and external partners.

we are seeking a Research Assistant
Key Responsibilities:
Implementing and executing lab techniques in cell biology and media development.
Developing and standardizing cellular in-vitro assays.
Evaluating and adopting lab practices and methods.
Culture media preparation
Writing scientific reports and procedures and data presentations to other R&D teams.
Ability to collaborate effectively within a team and work independently.
Ability to work in a dynamic and fast-changing environment.
This full-time position is in the Science Park, Ness Ziona, Israel (not far from the Rehovot train station).