לוח משרות דרושים ביולוגיה / בוטניקה משרה מלאה

we are a leading-edge company specializing in the design of multi-specific human antibodies, using AI and Machine Learning techniques, to cure patients. We are seeking a skilled and experienced Lab Technician and Equipment Specialist to join our team. The ideal candidate will perform essential laboratory tasks, operate FACS and Flow Cytometry devices professionally, Support lab personnel with equipment troubleshooting, perform training sessions and provide scientific support for our research processes. Responsibilities
* Operating and maintaining FACS, Flow Cytometers and other analytical equipment, ensuring proper function and calibration.
* Train and mentor R&D teams and provide scientific support to improve our research processes.
* Optimizing existing work protocols to enhance robustness and reduce operational costs.
* Routine maintenance for a wide range of laboratory equipment, coordinate maintenance services and repairs, and perform troubleshooting when needed.
* Routine maintenance of Tissue Culture lab, including performing Mycoplasma testing.
* Daily lab operations, including sterilizing lab equipment and general lab cleanliness.
* Comply with safety protocols and regulatory guidelines to ensure a safe working environment. Required Experience and Skills:
* Bachelors degree or higher in Biology, Chemistry, Biotechnology or a related field.
* At least 3 years of experience working in a lab environment, preferably in the biotech or pharmaceutical industry, Familiar with different laboratory techniques and equipment.
* Significant experience in operating and maintaining FACS and Flow cytometry instruments - MUST
* Strong organizational skills with attention to detail and the ability to manage multiple tasks simultaneously.
* Excellent communication and interpersonal skills.

we are a global publicly-traded commercial-stage oncology company developing a profoundly different cancer treatment therapy called tumor treating fields (TTFields) for patients with solid tumors. TTFields therapy is a non-invasive, novel, antimitotic treatment modality that utilizes proprietary technology attempting to slow or reverse tumor progression by inducing tumor cell death.
our company's commercialized product, Optune, is approved for the treatment of adult patients with glioblastoma (GBM) in the USA, Europe, and Israel.
our company has ongoing or completed clinical trials and is further expanding its efforts into several other solid tumor indications - non-small cell lung cancer, pancreatic cancer, and other types of solid cancers.
We are looking for a Researcher the biology research team in the preclinical department. As a Researcher you will be part of basic scientific research for the identification of the responses to electric fields in the molecular and cellular levels.
This is a full time position in our R&D center, Haifa, Israel, and reported to the
Senior Scientist.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
Effective experimental planning, preparation of protocols, conductance of experiments according to protocol, documentation of the results, interpretation of the results and preparation of a summary report in accordance with the highest scientific standards
Must be highly detail oriented and very well organized
Responsible for performing in vitro experiments according to good laboratory practice
Maintain personal and other employees safety.

we are a global publicly-traded commercial-stage oncology company developing a profoundly different cancer treatment therapy called tumor treating fields (TTFields) for patients with solid tumors. TTFields therapy is a non-invasive, novel, antimitotic treatment modality that utilizes proprietary technology attempting to slow or reverse tumor progression by inducing tumor cell death.
our company's commercialized product, Optune, is approved for the treatment of adult patients with glioblastoma (GBM) in the USA, Europe, and Israel.
We are looking for Biostatistics for our Biostatistics team.
As a biostatistician, you will contribute to the statistical aspects of our clinical trials.
The role will involve the usage and implementation of statistical techniques commonly used for Oncology clinical trials.
In addition, the role will include clinical SAS programming for data verification.
This is a full time, Hybrid position as part of our team in Isarel.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
Contribute to protocol development in conjugation with clinical development and operation teams and responsible to assess the feasibility of the study endpoints and develop the Statistical Analysis Plan (SAP)
Report the study results in the Clinical Study Report (CSR)
Oversight of the CRO and validate other vendors' statistical activities
Assist to provide statistical advice and advice on statistical aspects of clinical and preclinical projects
Approve statistical outputs: Table, Listing and Figures (TLFs) and the analysis datasets produced by the statistical programming team using SAS
Work within a multidisciplinary team and serve as a point of contact between clinical operation, CRO and SAS programmer within the statistical department
Provide statistical input to the study-related documents: study execution plans (including Data Management Plan), eCRF design and Edit Checks specifications, eCRF completion guidelines, data reconciliation plans
Review SAS coding and specifications
Other responsibilities as assigned.

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