לוח משרות דרושים בוגרי מדעי החיים משרה מלאה, לחיפוש זה נמצאו 72 משרות

we are looking for a FSP Clinical Research Associate I/ Clinical Research Associate II.
As part of our global team, you'll have the opportunity to perform and coordinate different aspects of the clinical monitoring and site management process. As a Clinical Research Associate I, you'll conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation. You will manage procedures and guidelines from different sponsors and/or monitoring environments (i.e., FSO, FSP, Government, etc.). Acting as a site processes specialist, you will ensure that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects' rights, well-being, and data reliability. You will ensure audit readiness and develop collaborative relationships with investigational sites. Detailed tasks and responsibilities assigned to your role are outlined in the task matrix.

We are seeking a highly motivated Quality Assurance Junior Specialist. The role is responsible for performing routine Quality Assurance tasks while also maintaining and continuously improving the implemented Quality Management System within the Israel affiliate.
What Youll Do:
Register and manage customer and HCPs complaints in the Trackwise system, ensuring compliance with division timelines.
Oversee the Batch Release process for our Nutrition products in line with global and local policies/regulations.
Review and manage invoice checks related to Batch Release activities.
Support Affiliate Training management in conjunction with the QA Supervisor/Manager.
Manage Document Control processes: initiate change requests, coordinate Subject Matter Expert (SME) edits, route documents for approval, and ensure timely completion and periodic reviews.
Review and evaluate Supplier Quality activities, including qualification, performance monitoring, audits, and SCAR (Supplier Corrective Action Request) closures, within required timelines.
Support inspection and audit readiness activities for the Affiliate, as directed by the QA Supervisor/Manager.
Assist in preparing Management Review presentations in collaboration with the QA Supervisor/Manager.
Monitor and support NCR (non-conformance) initiation, conduct root cause analysis, and oversee CAPA (corrective and preventative actions) implementation and effectiveness tracking.
Contribute to On-Market Events/Product Actions presentations in partnership with the QA Supervisor/Manager.

As a Digital Medical Advisor, you'll be at the forefront of how we communicate science in the digital age. You'll develop and execute medical strategies that strengthen our digital scientific communication and drive meaningful engagement with Digital Opinion Leaders (DOLs) across Israel.

Your responsibilities will include:
Driving comprehensive DOL engagement strategies from end-to-end - identifying, assessing, and cultivating relationships with key Digital Opinion Leaders to amplify scientific dialogue and foster compliant advocacy.
Developing tailored content, resources, and specialized workshops that resonate with digital audiences and advance scientific understanding.
Preparing, medically reviewing, and disseminating all corporate medical communications across digital platforms, ensuring scientific accuracy and regulatory compliance.
Creating planned medical scientific journeys for all relevant audiences, translating complex scientific content into impactful digital formats.
Collaborating with Marketing, Sales, Medical, Compliance, and Customer Excellence teams to align strategy, prioritize initiatives, and execute scientifically accurate, impact-driven programs.
Engaging with healthcare professionals and DOLs, to gather insights, co-create content, and ensure clinical relevance.
Driving innovation in digital engagement by adopting new channels and methodologies that support our digital-first Medical Affairs model.

We are looking for a Senior Clinical Application Engineer to serve as the clinical face of our robotic surgical system in the field. The Senior Clinical Application Engineer trains, demonstrates, and supervises surgeons and operating-room staff performing robotic-assisted ophthalmic procedures, supports clinical sessions on site, and brings structured clinical insights back to the Product and R&D teams. The role involves frequent international travel to clinical and training sites.

Responsibilities
Train and certify surgeons, nurses, and OR staff on the use of the robotic system, from didactic and wet-lab/simulator training through supervised live procedures.
Provide on-site clinical and technical support during surgical procedures, including system setup, draping, intra-operative guidance, and troubleshooting.
Demonstrate the system to surgeons, clinical teams, and KOLs at clinical sites, training centers, and conferences.
Plan and execute site onboarding: readiness assessments, OR integration, team training plans, and sign-off criteria for independent use.
Develop and maintain training materials, curricula, and proficiency assessments in collaboration with Product/HFE, R&D, and Regulatory teams.
Collect, synthesize, and report structured clinical feedback and usability observations from the field to product teams.
Support clinical studies: case observation, protocol adherence support, and coordination with clinical/regulatory staff.
Document and report field events, complaints, and device observations per the company's quality system and regulatory requirements.
Build and maintain trusted relationships with surgeons, clinical staff, and site stakeholders.

We offer hope to patients suffering from rare and severe diseases by 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 30 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! 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