לוח משרות דרושים מדעי החיים, טבע וחקלאות בתל אביב יפו

What if the work you did every day could impact the lives of people you know? Or all of humanity?
At our company, we are expanding access to genomic technology to realize health equity for billions of people around the world. Our efforts enable life-changing discoveries that are transforming human health through the early detection and diagnosis of diseases and new treatment options for patients.
Working at our company means being part of something bigger than yourself. Every person, in every role, has the opportunity to make a difference. Surrounded by extraordinary people, inspiring leaders, and world changing projects, you will do more and become more than you ever thought possible.
Job Title: Part-Time Technical Writer (MD Student)
Location: Hybrid/Remote (Israel-based preferred)
Hours: ~20 hours per week
Team: Clinical Genomics Platform
A part of our company, is the leading AI-based platform for genomic interpretation, empowering clinical labs and research teams to unlock the full potential of genomics. We build tools that assist clinicians and geneticists in understanding and interpreting genomic data, with the goal of enabling faster and more accurate diagnoses.
Position Overview
We are seeking a part-time Technical Writer with a medical background to join our team. This role is ideal for a current MD student with strong writing skills and an interest in genetics, bioinformatics, or clinical diagnostics. Youll help translate complex scientific and clinical content into clear, user-friendly documentation that supports our users clinical geneticists, lab professionals, and researchers.
Responsibilities
Write and maintain high-quality internal and external documentation for clinical features, product workflows, and knowledge base content.
Translate scientific and technical information into clear language for various audiences.
Collaborate closely with product managers, clinicians, engineers, and designers to gather content and understand new features.
Contribute to the creation of training, educational, and support materials for diverse healthcare audiences.

We seek a highly motivated and experienced Senior Researcher to join our dynamic team. This role is pivotal in advancing our collaboration with leading academic institutions and healthcare organizations globally and helping us deliver cutting-edge insights that support business growth and B2B opportunities. The ideal candidate will contribute to the entire research lifecyclefrom study design to publication.
Responsibilities
Research Collaboration:
Work closely with universities, academic institutions, and research teams worldwide to design, execute, and manage collaborative studies focused on metabolic health and performance.
Study Design & Execution:
Develop robust study designs tailored to explore metabolic health, fitness optimization, and related areas. Oversee the execution of studies, ensuring alignment with scientific standards and ethical guidelines.
Data Analysis & Insight Generation:
Analyze study and retrospective data to extract actionable insights that advance metabolic research and support our product development, marketing, and B2B initiatives.
Publication & Thought Leadership:
Lead the drafting and submission of high-quality manuscripts to peer-reviewed journals.
Innovation & Product Integration:
Collaborate with cross-functional teams to translate research findings into innovative product features, user education materials, and growth strategies.
Strategic Input:
Provide strategic insights to enhance our position as a metabolic health research leader. Identify new research opportunities that align with business goals.

Join our team as a Geo Analyst and join our experts team, which specializes in processing high-quality geographic data, databases, and layers, driving innovative solutions in the GIS world. Dive into technical research, automated process development, and critical decision-making to revolutionize real-time infrastructure data accessibility.
Responsibilities:
Process and analyze geographic data, databases, and tabular data with a focus on high-quality outputs.
Conduct technical research, assess the relevance and quality of geographic data layers, and make informed decisions regarding their usability.
Contribute to the development of broader automated processes aimed at enhancing data analysis capabilities.
Design tools for statistical analysis and automation to improve efficiency and accuracy in handling geographic data.
Utilize expertise in GIS and mapping to interpret and manipulate geographic data effectively.
Collaborate with team members to ensure the accuracy and relevance of geospatial information for real-time data product features.

Position: Program Manager.
The Program Manager is responsible for supporting and nurturing early-stage environmental initiatives and organizations (NGOs).
This is achieved through professional mentoring, strengthening organizational infrastructure, and refining the operational model with an emphasis on creating organizational and financial sustainability.
The role includes mentoring initiatives, managing a network of expert advisors, overseeing a training program, and developing partnerships.
Key Responsibilities:
Provide professional guidance to environmental initiatives in developing logical frameworks, building and implementing work plans, forming partnerships, fundraising, and more.
Manage the selection process for initiatives, including coordination with professional partners and foundations.
Recruit and support expert consultants in relevant fields (environment, sustainability, monitoring and evaluation).
Prepare regular reports for the programs steering committee.Identify additional resources for funding both the initiatives and the program.Build a professional community of initiatives, including workshops, learning sessions, and forums.
Monitor the progress of initiatives, identify challenges, and provide tailored support.
Plan and deliver professional training sessions.
Develop the programs resource base in partnership with the Resource Developer of the Life & Environment organization and the organization's CEO.
Employment Terms:Hybrid position: Three days a week at the office in Tel Aviv.
Scope: Full-time (100%).
For more details and to apply our email.
Applications accepted until June 14, 2025.

a rapidly growing medical technology company revolutionizing hematology and cell morphology analysis. Our mission is to facilitate quicker, earlier detection and diagnosis of blood-related diseases, ultimately leading to improved patient outcomes. At every team member plays a crucial role in our life-saving mission.

About our technology
developed a groundbreaking digital imaging platform utilizing innovative computational photography and clinical-grade AI. This platform automatically analyzes blood samples at the highest resolution available and delivers results within minutes. Our Full-Field Peripheral Blood Smear Application has received FDA clearance, and our technology is currently in commercial use across hospitals and labs in the US, Europe, and Israel.

What youll be doing
Collaborating with cross-functional R&D teams to enhance development and testing processes
Designing and developing test infrastructure, both back-end and front-end
Creating and executing comprehensive test plans, test suites, and test scripts to validate functionality, performance, integration, and security
Reporting metrics, test results, and defects to stakeholders
Developing, executing, and maintaining automated testing frameworks
Preparing and maintaining relevant documentation and technical guidelines

A fields of hematology and cell morphology analysis. As a team, we work to enable faster, earlier detection and diagnosis of blood-related diseases, so patients can start treatment sooner and have better outcomes. We are collaborative and global and every individual at is part of a life-saving mission.
About our technology
developed a digital imaging platform using novel computational photography. Built on top of this breakthrough technology is clinical-grade AI that automatically analyzes blood samples at the highest resolution available and in minutes. has secured FDA clearance for its Full-Field Peripheral Blood Smear Application and Full-Field Bone Marrow Aspirate Application and its technology is in commercial use at hospitals and labs in the US, Europe, and Israel.
About the position
We are seeking an experienced and dynamic Clinical Affairs Team Lead to join our growing company. This role is pivotal in ensuring successful execution of our clinical trial portfolio and alignment with regulatory and business objectives. The ideal candidate will have proven managerial and operational expertise in clinical trial execution and team leadership, coupled with a strong scientific background. This is an opportunity to lead a dedicated team and contribute directly to the success of the business.

What youll be doing
Clinical Trial Management: Lead and oversee the execution of multiple ongoing clinical trials, secure the successful completion of studies, and meet timelines and quality standards
Operational Excellence: Develop and optimize clinical trial processes, ensuring efficient workflows and compliance with regulatory standards
Stakeholder Collaboration: Act as the primary liaison between internal teams, external partners, and clinical sites to ensure alignment and effective communication
Regulatory Compliance: Ensure all clinical activities adhere to regulatory requirements, including those of FDA, CE, and other relevant authorities
Data Integrity: Oversee data collection, management, and reporting to ensure accuracy and reliability in support of regulatory submissions and business goals
Risk Management: Identify potential challenges and proactively implement solutions to mitigate risks to clinical trial success
Strategic Planning: Contribute to the development and execution of the clinical strategy in alignment with the companys goals and assume responsibility for clinical study design

a fast-growing medical technology company transforming the fields of hematology and cell morphology analysis. As a team, we work to enable faster, earlier detection and diagnosis of blood-related diseases, so patients can start treatment sooner and have better outcomes. We are collaborative and global and every individual at is part of a life-saving mission.
About the job
We are looking for a Quality Assurance Compliance Specialist to join our compliance and RA team, which plays a central role in both pre-market and post-market activities. The team is responsible for regulatory activities, quality management system, and ensuring compliance with applicable standards, including those related to privacy.

The Quality Assurance Compliance Specialist will play an important role in the companys regulatory, quality and compliance activities, such as ensuring compliance with relevant quality standards (including ISO 13485:2016, 21 CFR 820, MDSAP and IVDR); supporting internal audits, corrective efforts and different quality projects; and defining quality procedures, protocols and tools.

What youll be doing
Provide ongoing support for the companys quality management activities, including SDLC, PMS, product investigation, operations, training management, supplier management, and document control
Maintain the companys quality management system (QMS)
Evaluate and address quality assessment related to customer complaints
Prepare and maintain technical documentation in compliance with standards such as ISO 13485, 21 CFR 820, and IVDR
Collaborate with cross-functional teams, including R&D, product development, and technical support on quality-related activities
Perform privacy-related tasks, such as evaluating suppliers for privacy compliance and reviewing data processing agreements (DPAs)
Analyze post-market surveillance data to support company initiatives
Prepare teams for internal and external audits

a fast-growing medical technology company transforming the fields of hematology and cell morphology analysis. As a team, we work to enable faster, earlier detection and diagnosis of blood-related diseases, so patients can start treatment sooner and have better outcomes. We are collaborative and global and every individual at is part of a life-saving mission.

About the job
We are looking for a compliance analyst to join our compliance and RA team, which plays a central role in both pre-market and post-market activities. The team is responsible for regulatory activities, quality management system, and ensuring compliance with applicable standards, including those related to privacy.

The analyst will play an important role in the companys regulatory, quality and compliance activities, such as ensuring compliance with relevant quality standards (including ISO 13485:2016, 21 CFR 820, MDSAP and IVDR); supporting internal audits, corrective efforts and different quality projects; and defining quality procedures, protocols and tools.

What youll be doing
Provide ongoing support for the companys quality management activities, including SDLC, PMS, product investigation, operations, training management, supplier management, and document control
Maintain the companys quality management system (QMS)
Evaluate and address quality assessment related to customer complaints
Prepare and maintain technical documentation in compliance with standards such as ISO 13485, 21 CFR 820, and IVDR
Collaborate with cross-functional teams, including R&D, product development, and technical support on quality-related activities
Perform privacy-related tasks, such as evaluating suppliers for privacy compliance and reviewing data processing agreements (DPAs)
Analyze post-market surveillance data to support company initiatives
Prepare teams for internal and external audits