לוח משרות דרושים ביוטכנולוגיה משרה מלאה

We are looking for a hands-on Facilities & Lab Manager to take full ownership of our office and laboratory environments.
This role reports directly to the VP Operations.
Responsibilities
Own day-to-day operations of office & labs
Maintain, repair, and install infrastructure & equipment (hands-on / vendors)
Ensure a clean, organized, and fully functional work environment
Keep labs efficient and ready for fast-paced R&D work
Perform preventative maintenance on lab equipment
Work closely with R&D/engineering on experiments and new tools
Ensure labs support both development and production-scale activities
Manage external vendors and ongoing facility services
Own safety procedures and compliance (including storage & disposal of materials)
Responsible for company security
Lead renovation and construction projects.

At Medison, we offer hope to patients suffering from rare and severe diseases. Through strategic partnerships with best-in-class biotech companies we commercialize innovative therapies across global markets. Medison is a dynamic, fast?paced company operating in dozens of countries across five continents. We are looking for passionate, agile, and adaptive leader who want to make a real impact and help shape the future of global healthcare. Our culture is rooted in care, agility, collaboration, and innovation, and we’re united by a shared purpose to make a meaningful difference. If you’re passionate about driving growth and delivering breakthrough innovation to patients, we invite you to be part of our journey. Reporting to Medison’s Head of Business Development, the Director, Search & Evaluation Business Development is a mission?critical leadership role that directly shapes Medison’s long?term growth and strategic direction, while advancing our core purpose of improving and saving patients’ lives worldwide. The position plays a foundational role in building Medison’s future pipeline by identifying high?impact opportunities that expand global access to the most advanced therapies. In this role, you will proactively identify best?in?class assets, lead rigorous scientific and clinical evaluations, and drive cross?functional diligence to enable high?quality, strategic partnering decisions. You will operate at the intersection of science, strategy, and execution, working in close partnership with Medical, Regulatory, and senior leadership to support disciplined growth and long?term value creation.

Responsibilities:

* Proactively screen, source, and prioritize best?in?class late?stage assets from Phase 2 through marketed products across rare and severe diseases, leveraging multiple platforms, databases, and industry sources.
* Build and manage a robust and high?quality pipeline of partnership opportunities aligned with Medison’s long?term growth strategy.
* Lead rigorous scientific and clinical evaluations by assessing clinical data versus current standard of care, mechanism of action differentiation, regulatory pathways, and competitive landscape.
* Develop clear and data?driven Target Product Profiles (TPPs) to support scientific, clinical, and strategic positioning.
* Conduct comprehensive research, including literature review and data synthesis, to deeply understand disease biology, unmet need, and therapeutic value.
* Engage directly with Key Opinion Leaders, clinical investigators, and external experts to validate assumptions and strengthen scientific and clinical assessments.
* Drive cross?functional diligence by partnering closely with function leads, Medical and Regulatory, Commercial, Legal, Finance, and other relevant stakeholders.
* Support transaction strategy and execution by providing scientific and clinical input into transaction strategies, diligence materials, and contractual discussions.
* Prepare clear, concise, and decision?ready materials, including evaluation summaries, one?pagers, presentations, and business cases for senior leadership and governance forums.
* Continuously refine and strengthen Search and Evaluation processes, criteria, and scientific convergence frameworks to improve rigor, consistency, and speed of decision?making.
* Act as a trusted thought partner to leadership by surfacing insights, risks, and recommendations that directly influence portfolio strategy and Medison’s growth trajectory.
* Represent Medison externally in partnering discussions, scientific meetings, and industry conferences to strengthen Medison’s visibility and network.

City:
Petah Tikva

we are a leading silicon photonics company developing advanced solutions for data center connectivity.
We are looking for a hands-on Facilities & Lab Manager to take full ownership of our office and laboratory environments.
This role reports directly to the VP Operations.
Responsibilities
Own day-to-day operations of office & labs
Maintain, repair, and install infrastructure & equipment (hands-on / vendors)
Ensure a clean, organized, and fully functional work environment
Keep labs efficient and ready for fast-paced R&D work
Perform preventative maintenance on lab equipment
Work closely with R&D/engineering on experiments and new tools
Ensure labs support both development and production-scale activities
Manage external vendors and ongoing facility services
Own safety procedures and compliance (including storage & disposal of materials)
Responsible for company security
Lead renovation and construction projects .

We are looking for R&D Pharma Team Leader to be responsible for the professional and managerial leadership of R&D pharma team engaged in formulation and process development of drug products. The role includes building and executing work plans, managing timelines, providing scientific expertise of formulation and manufacturing process development, scale-up activities, transition of products from development to commercial manufacturing, leading process validations and technology transfers and supporting ongoing commercial manufacturing through deviation investigations and professional assessments, while continuously driving operational efficiency within the department.

Responsibilities:
Serve as a subject matter expert in formulation development, scale-up, and manufacturing processes.
Assign tasks, prioritize activities, and perform continuous follow-up on execution.
Ensure high-quality scientific and technical deliverables in compliance with GMP and regulatory standards.
Lead formulation and manufacturing process development in accordance with QbD methodology. Definition of QTPP, CQAs, CPPs, and Design Space.
Evaluation of experimental work, including scale-up activities from laboratory scale to Engineering to registration batches scale.
Lead and support process validation activities (Process Validation, PPQ). Review, assess, and approve validation protocols and reports.
Lead and participate in pharmaceutical technology transfer projects and transition of drug products from development status to commercial manufacturing, ensuring process robustness, regulatory readiness, and manufacturing continuity.
Collaborate with QA, Regulatory Affairs, Manufacturing, and Engineering to ensure successful product commercialization.
Identify risks, delays, and resource gaps, and lead mitigation actions.
Provide regular progress updates to management.
Actively participate in deviation investigations related to products in routine manufacturing and provide professional pharmaceutical opinions and assessments.
Perform root cause analysis and support definition and implementation of CAPAs.
Support change control activities related to products and processes.
Initiate and lead continuous improvement and efficiency initiatives within the department.
Implement pharmaceutical and regulatory best practices.

To apply, please send your application to our e-mail.