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

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