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If you're a Java expert and looking for a workplace that will respect your passion to learn and expand your knowledge - you've come to the right place!
We are a platform that enables large companies to
maximize their profits from their Amazon activity.
The platform consists of
products that optimize pricing and advertising by collecting and processing
*terabytes of data a day* and is backed by advanced algorithms based on AI.
Today, we are entering the market of enterprises, brands and
vendors and therefore adding new products that will meet the high scale waiting
for us. As part of the development of these new products we are looking for Senior Back End Engineer.

Cell Therapy Quality Control Specialist Flow Cytometry
Advanced Biotherapy Center
Sheba Medical Center, Tel Hashomer
We are looking for a highly motivated individual to perform analytic assays for experimental cell and gene therapies for patients in clinical trials. Your main focus will be on designing and performing flow cytometery assays. You will also perform assays using various techniques including qPCR, ddPCR, ELISA, and bacterial culture.
You will work with various TEST materials including viral vectors, cell banks, primary human cells, and human blood. You will be part of a small team performing required QC assays for both Sheba projects and outside customers. Experience with analytic assays and cell culture in biotech, or pharma laboratory is preferred.
Excellent written English is required. This work may lead to publications in scientific journals and will support clinical trials for treatment of patients with cancer and other types of disease.
Sheba Medical Center is developing and manufacturing new cell and gene therapies for patients with serious diseases. The job holder will report to Dr. Jonathan Esensten at Sheba Medical Center.

We seek a customer-focused Technical Support Engineer to join our dynamic support team.
As a Technical Support Engineer, you will provide exceptional technical assistance and troubleshooting to our clients, ensuring their seamless experience with our platform. Your expertise and dedication will be crucial in driving customer satisfaction and loyalty.
In this role you will:
Develop a deep understanding of our data integration platform, staying up-to-date with new features and enhancements
Deliver timely and effective technical support via various channels, including ticketing system and online meetings, addressing inquiries, issues, and concerns promptly and professionally.
Investigate and resolve technical problems reported by clients, escalating complex issues to the appropriate teams for resolution.
Collaborate closely with cross-functional teams, including product development and engineering, to ensure prompt issue resolution and continuous product improvement.
Assist in conducting product training sessions for clients, empowering them to utilize our platform efficiently.
Accurately document support cases, tracking their progress from initiation to resolution and keeping clients informed throughout the process.
Contribute to the development and maintenance of our knowledge base, creating helpful articles and resources for self-service support.

We are looking for a Clinical Affairs Manager to implement and oversee all activities related to clinical research and clinical studies in the company.
DiA Imaging Analysis provides AI-powered solutions to make ultrasound image analysis smarter and more accessible.
Its AI-based solutions help ultrasound users acquire the right image and analyze it automatically, allowing them to identify clinical abnormalities that are often difficult to find visually and enabling them to make better decisions based on accurate and objective data.
Your role:
Designing and managing the execution of clinical studies that demonstrate medical product safety and efficacy.
Ensuring that trials are conducted in full compliance to GCP.
Full responsibility on sites initiation, site personnel training and monitoring.
Working closely with the principal investigators and study coordinators.
Working with regulatory, development and marketing teams to create scientific publications, clinical marketing material and clinical background required for regulatory submissions.