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 looking for a Clinical and RA associate.
Primary function of the position
Under the oversight of the CRA manager (CTM) the person ensures compliance of study conduct with ICH/GCP and country regulations, companys policies and procedures, quality standards and adverse event reporting requirements internally and externally.
Acts as primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility of allocated sites.
Roles and responsibilities:
Develops strong site relationships and ensures continuity of site relationships through all phases of the trial.
Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs, Local Laws & Regulations, Protocol, Site Monitoring Plan and associated documents.
Gains an in-depth understanding of the study protocol and related procedures.
Coordinates & manages various tasks in collaboration with other sponsor roles to achieve Site Ready.
Performs remote and on-site monitoring & oversight activities using various tools to ensure:
Data generated at site are complete, accurate and unbiased
Subjects right, safety and well-being are protected
Conducts site visits including but not limited to initiation visits, monitoring visits, close-out visits and records clear, comprehensive and accurate visit & non-visit contact reports appropriately in a timely manner.
Collects, reviews, and monitors required regulatory documentation for study start-up, study maintenance and study close-out.
Communicates with Investigators and site staff on issues related to protocol conduct, recruitment, retention, protocol deviations, regulatory documentation, site audits/inspections and overall site performance.
Supports and/or leads audit/inspection activities as needed
Following the country strategy defined by CRD and CTM, contributes to the identification of new potential sites and works closely with them to develop strong clinical research capabilities
Whiling to travel abroad including US for sites oversights

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.

forming partnerships with emerging biotech companies to accelerate access to highly innovative therapies in international markets.
As the creator and leader of the global partnership category in the pharma industry, we strive to be Always Ahead and work relentlessly to bring therapy to patients in need, no matter where they live.
Our values are at the core of every action we take, and we are committed to going above and beyond for the benefit of the patients we serve.
We are a dynamic, fast-paced company operating in over 25 countries on 5 continents. We are looking for out-of-the-box thinkers, people who are passionate, caring, agile, and adaptive, to join us on our mission. If you want to make a difference in people's lives, we invite you to join us!
looking for a Sales Representative for the Aesthetics Unit.
This role includes Sales to dermatologists, plastic surgeons, and physicians for cosmetic use in private clinics in the northern area.

Responsibilities
In-depth knowledge of the market and competitors.
In-depth understanding of products and full portfolio.
Establishing personal relationships with existing customers and identifying and recruiting new customers.
Identifying customer needs and finding applicable solutions.
Selling products to physicians who perform injection procedures at their private clinics and medical centers.
Participating in conferences and workshops in Israel and abroad.

A pioneering med-tech company developing innovative inhalation technologies for precise drug delivery. Our mission is to enhance patient care by leveraging breakthrough technology to improve treatment outcomes.

We are looking for a cQP (Cannabis Qualified Person) & cRP (Cannabis Responsible Person) to join our Tiberias site. As cQP (Cannabis Qualified Person) youll ensures that each batch of product released for marketing is produced and tested in accordance with the quality and regulatory requirements.

As cRP (Cannabis Responsible Person) youll be responsible for drugs inventory movements in the facility and for fulfilling regulatory requirements. Moreover, ensures that each batch of product released for marketing is produced and tested in accordance with the quality and regulatory requirements.
Key Responsibilities
Responsibilities as cQP
Releasing cartridge production batches to the market after approval of quality assurance, ensuring compliance with regulatory and quality requirements, adhering to Eudralex volume 4, annex 16, guidelines.
Batch release approval documents will be personally kept by the CQP, available for authorities review, for a period of no less than 5 years.
Supervision of the production of cannabis products.
Change controls regarding manufacturing process review and, when applicable, plan approval.
Participation in solving quality issues and deviations in production.

Responsibilities as cRP
Contact with the relevant district pharmacist on issues related to the production or release of products.
Dangerous Drugs inventory log management.
Dangerous Drugs annual report to the IMCU: Preparation of annual reports for submission to the district pharmacist.
Control over the receipt of cannabis into the warehouse.
Supervising the preparation of shipments of finished products.
Preparation of rejected cannabis for destruction including full documentation.
Carrying out a monthly and annual cannabis inventory count.
Change controls regarding inventory management and procedural cannabis movements review and, when applicable, plan approval.
Control of procedures as needed.

Are you passionate about making a difference in the lives of people living with Obesity? Do you have a knack for building impactful strategies and fostering meaningful relationships? If so, we invite you to join our company as our new Obesity Consumer Engagement Product Manager. Read on and apply today for a life-changing career!
The position
As an Obesity Consumer Engagement Product Manager at our company, you will play a key role in transforming people living with obesity experience care and support. This is your opportunity to lead meaningful change by putting patients at the heart of everything we do. You will drive new and innovative ways to establish focused strategy to reach out people living with Obesity and Patients already on our innovative obesity treatments. Through cross-functional collaboration and a patient-first mindset, youll be at the forefront of launching impactful initiatives that support both individuals and the healthcare ecosystem.
Your main responsibilities will include:
Leading the launch excellence of anti-Obesity medication, ensuring a smooth and impactful introduction to the market for patients.
Crafting and executing an integrated engagement strategy tailored to the needs of people living with obesity.
Designing strategic communication plans and building meaningful partnerships to increase awareness and impact.
Collaborating with the medical community through scientific dialogue and supporting updates to medical guidelines.
Driving market access efforts, aligning with key stakeholders and payers to ensure broader availability of our treatments.