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Were hiring a Medical Lead!
If youre looking for a meaningful role that blends science and collaboration, and you enjoy driving scientific initiatives and supporting product launches, wed love to meet you.
Responsibilities:
Represent the company before current and prospective business partners/customers, focusing on scientific aspects.
Prepare applications for the inclusion of new products in the Israeli Health Basket.
Introduce new products to Israeli health funds.
Lead discussions with Key Opinion Leader physicians and deliver enrichment lectures to professional audiences.
Present and participate in the companys advisory board for physicians, addressing questions and expanding scientific knowledge.
Analyze opportunities for new products for the Israeli market, including product details, relevant diseases, market, competition, etc.
Evaluate competing products while understanding marketing and commercial needs.
Provide consultations on the content of marketing materials.
Develop and train medical learning materials, such as training booklets and presentations, and offer training to new representatives and enrichment for other company employees.
Support clinical submissions to the Pharmacy Department of the Israeli Ministry of Health, necessary for updating indications and dosage regimens.
Coordinate and sign medical agreements with manufacturers abroad.

We are looking for a Technology Transfer project manager to be responsible for leading and coordinating end-to-end technology transfer projects for drug products. In this role is you will be responsible for ensuring the successful transfer of products from different site within Israel to commercial production ensuring compliance with GMP, regulatory requirements, quality standards, timelines, and budget.
Responsibilities
Lead pharmaceutical technology transfer projects from initiation through completion in accordance with established project management methodologies.
Management of all detailed project plans and action items according to the project's timeline, budget, and risk mitigation strategy.
Coordinate cross-functional teams including R&D, Analytical Development, Quality Assurance, Regulatory Affairs, Manufacturing, Engineering, Supply Chain, and external vendors.
Ensure all project activities comply with cGMP, Israeli Ministry of Health (IMOH) regulations, and relevant ICH guidelines
Manage project-related change controls, deviations and risk assessments in accordance with company quality systems.

we are a fast-growing, global leader in energy-based solutions for Aesthetics and Eye-Care. We are based in Yokneam, Israel (with offices in Tel-Aviv) with a strong business performance worldwide.
We are looking for a Clinical Manager for the Aesthetics Business Unit, which includes a broad portfolio of leading solutions in the market as well as an exciting innovation pipeline. The Clinical Manager will be responsible for pre and post-market activities for the assigned platform including: clinical requirements guiding design input, pre-clinical testing, clinical input to regulatory submissions, market conditioning for new solutions, post-market evidence generation and KOL development. The individual will serve as a major pillar in building relationships with global KOLs and demonstrating the clinical value and benefits of the solutions.
Key responsibilities:
Develop and manage clinical project plan, timelines, and budgets end to end; clinical research, through pre-clinical evaluations, clinical trials and publications, to user guidelines and post-market evidence generation.
Form and cultivate strong collaborative relationships with cross-functional partners in R&D, product, marketing, and regional teams
Coordinate internal cross-functional teams, as well as external clinical research associates, data managers, and biostatisticians
Oversee the execution of clinical studies, ensuring adherence to protocols and regulatory requirements
Lead the clinical input and support for key regulatory submissions and processes: regulatory submission clinical input, clinical validations, CER, CDP, CEP and more
Support marketing/commercial activities from the scientific/medical point of view: review and input to marketing collateral, develop white papers, active participation in scientific meetings and more
Communicate project status to stakeholders and provide updates on milestones and deliverables
Identify potential risks and implement mitigation strategies to ensure project success.

We are looking for a motivated and detail-oriented Clinical Affairs Manager to support the validation and evidence generation of our innovative professional and home-use aesthetic beauty devices. This role combines hands-on product efficacy evaluations and testing, oversight of external clinical evaluations, and translation of results into compelling, evidence-backed product claims.
While formal clinical studies are conducted by third-party partners, the Clinical Affairs Manager will also lead in-house validations using tools such as VISIA skin imaging systems and other skin analysis technologies to guide the development process of our next generation aesthetic devices. The goal is to ensure our devices demonstrate consistent, measurable results throughout development and to generate supporting data for product sales materials.
Key Responsibilities
1. In-House Product Testing & Efficacy Validation (Hands-On)
Plan and execute in-house clinical efficacy validations using skin analysis tools (e.g., VISIA or similar imaging/measurement systems)
Develop appropriate testing protocols, ensuring repeatability, accuracy, and meaningful endpoints
Maintain rigorous data logging, documentation, and participant tracking
Analyze results and produce clear reports, visuals, and key insights for internal decision-making
Work with R&D and Product teams to maintain clinical efficacy across development and provide feedback for improvement
2. Oversight of External Clinical & Consumer Studies (Vendor-Managed)
Define study requirements and intended claims, then work with external labs, dermatologists, or research agencies to design the study plan
Review and approve third-party proposals, ensuring the scope and methods support real-world product use and claim needs
Follow up during study execution via check-ins, milestone reviews, and data snapshots
Review and assess final results to ensure data quality and relevance
3. Evidence Generation & Claims Support
Translate internal and external tests results into clear, accessible messages for sales teams, distributors, and customers
Work with Product and Marketing to create evidence-backed claims, infographics, visuals, and storytelling
Ensure consistency between clinical findings and commercial messaging
4. Training & Clinical Communication
Deliver product and clinical training to internal teams and external partners (distributors, clinics, aestheticians)
Develop training materials that use validation data in a clear, credible way
5. Cross-Functional Collaboration & Practitioner Feedback
Serve as a point of contact for partners, KOLs, and testing partners
Gather user feedback and incorporate insights into study plans or product improvements
Work closely with R&D and Product teams to ensure alignment between testing, development, and launch needs
6. Scientific Awareness
Conduct focused literature reviews to support product rationale and claims
Stay informed about aesthetic device trends, skincare science, and relevant testing methodologies.