לוח משרות דרושים כימאי משרה מלאה, לחיפוש זה נמצאו 54 משרות

Required postdoctoral
a postdoctoral position is available in the laboratory of prof. alla zak. the lab focuses on the synthesis and characterization of inorganic nanomaterials for various applications.
the position is for one year, with the possibility of extension.

we are seeking a highly skilled Chemical/Polymer/Materials Engineer to join our dynamic team. The ideal candidate will be responsible for developing and improving materials and processes to enhance the performance and durability of our products. This is an exciting opportunity to work on cutting-edge projects in a an innovative environment.
Responsibilities:
Optimize Formulations and Processes: Improve product performance through new formulations and processes.
Conduct Research and Experiments: Test the properties and performance of materials to support development and innovation.
Collaborate Across Teams: Work with cross-functional teams to ensure material compatibility and integration.
Data Analysis and Reporting: Analyze data and provide detailed reports with findings and recommendations.
Material Testing and Quality Control: Manage material testing and ensure quality control procedures are followed.
Stay Current in the Field: Keep updated with the latest advancements in materials science and engineering.
Provide Technical Support:

we are seeking a highly skilled and experienced Senior Chemistry Researcher to join our innovative team. This role involves leading advanced research projects, developing new formulations, and optimizing processes to enhance our product offerings.
The ideal candidate will possess a deep understanding of chemistry and materials science, along with a proven track record of success in a research environment. .
This role requires a strong background in conducting independent research, publishing findings, and leading projects aimed at developing new materials and enhancing existing processes.
Duties and Responsibilities:
Lead and manage complex research projects focused on the development of new formulations and chemical processes.
Design and conduct experiments to test hypotheses and analyze results.
Collaborate with cross-functional teams to integrate research findings into new product development.
Prepare detailed technical reports, research papers, and presentations to communicate findings to stakeholders.
Mentor and guide junior researchers, providing technical expertise and support.
Stay current with industry trends, advancements, and regulatory requirements to ensure the company remains at the forefront of the field.
Contribute to the development of patents and intellectual property protection for novel discoveries.

we are looking for a QC Specialist.
Responsibilities:
Perform laboratory and environmental tests to assess the quality of raw materials, production areas, processes, and finished products.
Assist the QC Manager in developing and implementing laboratory methods, quality control procedures, and related documentation.
Execute validation protocols for equipment and processes.
Coordinate testing with external contract laboratories.

Medison is addressing one of the pharma industry’s most pressing challenges: enabling access to breakthrough therapies for patients with severe and rare diseases in international markets where traditional commercialization models fall short. As the creator and leader of the global partnership category, Medison has built a first-of-its-kind unified commercialization platform that enables biotechs to effectively plan, optimize and launch their therapies on a global scale. With a strong leadership team and a proven track record, Medison is the partner of choice for innovative biotech companies seeking to expand beyond the US, Western Europe and Japan into regions where most of the world’s population resides. Medison’s affiliate-like model integrates commercial, medical and operational capabilities across diverse geographies, accelerating access and delivering life-changing treatments to more patients, faster. Medison is on a mission to ensure that every patient, regardless of where they live, has the opportunity to benefit from breakthrough therapies. The Regulatory Affairs Specialist works in the pharmacy division. Preparation of registration portfolios – including checking that contents are according to regulations, writing consumer manuals, designing packaging, attending to changes/renewal/updates including stringencies with manuals, and supporting all activities in the pharmacy division.

Responsibilities:
Field of responsibility
* Preparation of all types of submissions –products, renewals, variations, leaflets and packaging.
* Responsibility for maintaining up-to-date product regulatory dossier.
* Direct contact with the Ministry of Health and partners abroad.
* Conducting regulatory and document checks.

City:
Petah Tikva