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We are hiring a Geographic Asset Surveyor to join our team and support real estate and asset consulting projects.
Key Responsibilities:
Collecting data and information from various geographic information databases.
Analyzing permit plans, area calculations, and financial data.
Conducting field surveys for geographic data collection.
Producing and regularly updating reports.
No prior experience required - full training provided by the company!

We are looking for a Quality Engineer to join our Ink Plant.
This role combines responsibility for plant quality activities with ownership of the day-to-day laboratory operations. The position plays a critical role in supporting production continuity, ensuring product quality, strengthening process control, and leading investigations and continuous improvement initiatives.
The ideal candidate is analytical, structured, comfortable working under pressure, and motivated to grow within a dynamic manufacturing environment.
What should you have?
Quality Responsibility:
Lead deviation investigations and root cause analyses
Manage non-conformances and drive corrective and preventive actions (CAPA)
Strengthen in-process controls and quality monitoring systems
Support batch release decisions in alignment with plant procedures
Drive standardization, documentation improvements, and KPI tracking
Analyze quality trends and provide data-driven recommendations
Support audits and ensure compliance with internal quality standards
Laboratory Operations Responsibility:
Take responsibility for the day-to-day operation of the laboratory
Ensure timely testing and responsiveness to production needs
Perform hands-on laboratory testing and analysis as required
Maintain testing standards, documentation accuracy, and procedural compliance
Optimize laboratory workflows and improve operational efficiency
Work closely with Production, Engineering, Planning, and Supply Chain to ensure smooth plant operations.

Required Application Development Technical Lead
Reports to: Application Development Manager
Location: Afek Industrial Park, Rosh Haayin
What Will You Do?
Lead the system process development for new technologies in the textile printing industry (including new inks, workflows, and systems).
Develop applications and conduct experiments to test and refine innovations.
Plan and conduct experiments using existing systems and prototypes
Develop and deliver optimized solutions with clear performance status and measurable KPIs
Identify gaps in existing processes, propose, and define improvements. Map gaps, opportunities and suggest performance envelope improvements
Draft specifications (software and PRD), define project steps, procedures, and test plans.
Analyze, summarize and present multi component complex issues, using methodological troubleshooting skills.
Act as a bridge between R&D, marketing, and customer needs, becoming an expert in the application of technology to customer requirements.
Analyze complex, multi-component challenges and provide solutions.
Provide support to Customer Service and other Development departments as needed.
Independently manage projects and tasks from initiation to completion.

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.

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

Required V&V Engineer
Location:
Afek Industrial Park, Rosh HaAyin
Reports to:
DTG Manager (QA)
V&V Engineer ensures that our products meet all system requirements, adhere to specifications, and deliver a high-quality, competitive solution that fulfills customer needs and expectations.
What will you do?
Serve as the Verification & Validation focal point
for a dedicated program within an Agile team.Conduct requirements and PBI analysis , as well as risk assessment and comprehensive test planning.
Design and execute tests at all levels - from software standalone to full system integration, including black box and grey box testing at the system level.
Define and develop automated tests to support both V&V and R&D activities.
Analyze, document, and report test results , ensuring accurate defect logging and tracking to resolution.
Monitor and follow up on defects and open issues through their full lifecycle.
Collaborate with development teams to provide actionable feedback, support fault isolation, and maintain high-quality data handoffs.
Identify and investigate cross-product issues and dependencies.
Support the Service and Field teams in resolving escalated customer issues and contributing to root cause analysis.

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.

Review micro-architecture specifications

Supervise verification team members and provide professional guidance

Implement Verification environment UVM based

Collaborate with Design engineers to resolve bugs and achieve coverage closure

Work with the firmware/Lab teams to verify chip flows

Perform debug, root-cause analysis, and post-silicon validation in the lab

You'll be joining our Silicon One Signal & power Integrity team, which is at the center of the silicon development at Cisco. Our SIPI engineers deal with all system development aspects and deliver detailed specifications to other development team. As SIPI engineer youll be required to design and analyze high speed analog/digital signals for networking products, with emphasis on high speed signal and power analysis of ASIC, Package and PCB. Model/simulate/characterize high speed systems, including high speed I/Os, chip packages, printed circuit boards, and system interconnects. Overcome the challenges of ultra-high data rate and cutting-edge technology. We use the latest silicon technologies and processes to build largest scale and most complex devices at the edge of feasibility.

Develop advanced verification environments using SystemVerilog and UVM
Write, run, and debug testbenches to ensure complete functional coverage
Drive pre-silicon and in-lab debug activities to resolve complex issues
Collaborate with RTL, architecture, and physical design teams to achieve design closure
Support methodology development, scripting, and automation to enhance productivity

Develop advanced verification environments using SystemVerilog and UVM
Write, run, and debug testbenches to ensure complete functional coverage
Drive pre-silicon and in-lab debug activities to resolve complex issues
Collaborate with RTL, architecture, and physical design teams to achieve design closure
Support methodology development, scripting, and automation to enhance productivity
Contribute to the success, powering the next generation of Internet infrastructure

In this role, you will be part of the Silicon One Switch ASIC Post-Silicon Electrical Validation (EPSV) team.
* Ensure the ASIC operates according to specifications and reliably over time by performing extensive, high-precision measurements using advanced test equipment and procedures.
* Conduct deep-dive investigations, integrating knowledge across hardware, software, and system domains to identify root causes of observed device behavior.

* Handle all chip validation aspects, including:
* Building validation plans.
* Deloping ASIC software test infrastructure.
* Writing tests in Python/C++ over device SDK.
* Executing tests and analyzing results.