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We are looking for an experienced Health, Safety and Environmental engineer to lead the EHS activities at our Netanya Site & Hadera warehouse in Israel. This role provides leadership and technical guidance in order to develop, implement, maintain and continuously improve of the Environmental, Health and Safety (EHS) Management System in order to guarantee full compliance with legal requirements and corporate EHS standards.


Responsibilities include but will not be limited to the following main tasks:


--Manage site EHS programs, including routine risk assessments, facilitating corrective measures as necessary and anticipating program needs based on relevant business conditions and EHS requirements.

Maintain and drive continuous improvement to the site EHS Program, procedures, and systems in accordance with local regulation and company requirements

- Acting with considerable independence, influence site staff activities to ensure site-wide EHS compliance and drive personal ownership and accountability for all employees.

- Ensure facility EHS compliance with local, National and corporate standards and guidelines.

- Develop, implement and maintain site-specific EHS programs including the recognition and reporting of any potential non-conformities with appropriate corrective actions.

- Interact and communicate with corporate EHS, Quality, Engineering, Manufacturing, and Research & Development staff

- Develop and deliver site-specific EHS training to meet facility needs; including regulatory and best management practices.

- Support proper investigations to determine root cause for all facility incidents, spills, accidents, near misses, and injuries to prevent recurrence.

- Coordinate proper handling and disposal of facility waste materials.

- Advise management on upcoming EHS regulations.

-Implement and track EHS initiatives at the site aligned with global corporate expectations and requirements.

- Maintain Local and corporate EHS reports, licenses, permits and performance indicators updated according to requirements.

We are looking for a Software Engineer specializing in ML Systems Engineering to join Finals Development department.

While vision and language models have become increasingly commoditized, Finals proprietary deep learning models are unique, fast-evolving, and deployed in live trading across the worlds most efficient and sophisticated financial markets. Operating in this environment presents distinct scaling challenges and continuous opportunities for optimization. Success in this role requires first-principles thinking and a deep understanding of the engineering trade-offs behind high-performance DL systems.

This is a pivotal role within Finals engineering organization. You will work closely with researchers and engineers across the company, running deep learning models on massive compute clusters and adapting them for production serving under strict and non-trivial constraints.

We are looking for an experienced and commercially driven leader to accelerate the growth of our Dairy Milking & Automation business across the EURAM region.

Milking & Automation is a strategic growth platform for our Company Animal Health, supporting our ambition to strengthen our role in connected dairy ecosystems, create greater value for customers and accelerate the adoption of data-driven livestock technologies.


Working closely with Global, Regional and Local teams, you will help translate innovation into customer value, market adoption and sustainable commercial growth through business development, portfolio commercialization and strategic partnership building.


Main Responsibilities

Drive the commercial growth strategy for the Dairy Milking & Automation portfolio across the EURAM region.
Identify market opportunities, customer needs and strategic initiatives to accelerate business expansion.
Lead portfolio commercialization activities, including go-to-market strategies, product launches and innovation deployment.
Develop business cases and recommendations to support investment decisions, geographic expansion and portfolio prioritization.
Build and strengthen relationships with dealers, distributors, customers and key industry stakeholders.
Partner with local Business Units to enhance commercial readiness, customer adoption and business performance.
Lead cross-functional projects and collaborate with Global, Regional and Local stakeholders to execute strategic initiatives.
Monitor business performance, market trends and forecasting insights to support strategic planning and decision making.

A fast-growing global medical device company that develops and manufactures innovative drug-delivery and infusion solutions across the continuum of care, from hospital to home. We are looking for an experienced V&V Manager to lead our V&V function and team within the R&D
Job Description:
Lead the V&V function and define the verification and validation strategy for new products and design changes.
Manage, develop, and provide technical leadership to a multidisciplinary team of V&V engineers, including goal setting, workload allocation, mentoring, and performance development.
Ensure complete, risk-based test coverage and traceability from product and system requirements through test evidence and final reports.
Review and approve V&V plans, protocols, reports, deviations, and supporting technical documentation.
Oversee system-level hardware, software, mechanical, and disposable-set testing in the R&D laboratory and at external laboratories and subcontractors.
Lead experimental design, data analysis, structured problem-solving, and root-cause investigations.
Plan resources, equipment, schedules, and priorities, and monitor execution against project milestones and quality objectives.
Partner with Systems, R&D, Quality, Regulatory, Clinical, and Project Management teams, and provide V&V support during audits and regulatory submissions.
Reports to: R&D Director.

Required QA Specialist
Description
An international Medical Device company that develops and manufactures innovative medical equipment. Specifically, we develop infusion pumps and their related accessory products.
Job Description:
supplier approval/disapproval including supplier maintenance and issuance of the Approved Supplier List.
Leading the SCARS process including SCAR initiation, SCAR follow up, Supplier investigation approval including root cause analysis and SCAR closure.
Leading the supplier audits process (including initial and surveillance audits) for critical suppliers, service centers, laboratories etc. by conducting on site / remote audits. Issuance and execution of the supplier audits plan including supplier audits follow up and supplier non-conformance follow up and response approval.
Support the execution of service agreements, quality agreements with suppliers and service centers.
Leading the supplier score card process, including trending.
Serve as Medicals CAPA Coordinator and Subject Matter Expert
Responsible and accountable for CAPA ownership, timely execution, and effectiveness of CAPAs. This includes creation, collaboration with functional teams on Problem Statement writing/Scope identification/Risk Assessment/Containment/Correction/CAPA plans/Verification of local and global compliance to CAPA procedures to ensure timely effective closure of CAPAs
Generate data and key quality trending information for use in periodic reviews like Quality Metric Reviews and Management Review for CAPA and supplier processes.
Work within, and ensure adherence to Quality System procedures, work instructions and other Quality System requirements.
Write, update, release, and sign quality documentation within the Quality management system
Direct manager: QA Compliance Manager

We are seeking a Clinical Project Manager to support the sourcing, handling, and management of biological samples and associated clinical metadata from academic collaborators, commercial biobanks, and clinical research centers. This role involves coordinating with suppliers (hospitals/research institutes/biotech companies), regulatory bodies, and internal teams to secure the necessary biological materials for research and development.
The CPM will play a key role in translating internal research needs into actionable collaborations, managing projects end-to-end from feasibility through sample delivery and data return to collaborators.
This role sits within the Cohort Acquisition Team within the Data group and reports to the Senior Clinical Project Manager.
Location: Ramat Gan, Israel (hybrid model)
What will you do?
Manage multiple sample acquisition projects, from initiation through delivery.
Oversee handoff and tracking of samples through internal processing pipelines.
Track milestones, risks, and dependencies across internal and external stakeholders.
Work closely with internal stakeholders to provide regular updates on sample availability, quality, and timelines.
Align expectations across teams and ensure smooth communication.
Support identification and evaluation of potential sources (academic centers, biobanks, CROs) and sample cohorts (cohort availability, sample types, clinical annotations, timelines).
Serve as a day-to-day point of contact for collaborators.
Track and resolve operational issues (delays, quality concerns, missing data).
Maintain clear documentation of project scope, status, and outputs.
Maintain and leverage a database of existing collaborations.
Enforcing quality standards, including complying with our internal standards.

We are looking for best-in-class Chip Design Engineers to join our outstanding Networking Silicon engineering team, developing the industry's best high speed communication devices, delivering the highest throughput and lowest latency! Come and take a significant part in designing our groundbreaking and innovative chips, enjoy working in a meaningful, growing and highly professional environment where you make a huge impact in a technology-focused company.

What you will be doing:

Join the Tel Aviv or Beer-Sheva group, working on RiscV processors platform.

Verification for chip blocks according to specifications under challenging constraints and with high orientation to power, area and performance.

Daily work might involve any or all aspects of chip development including verification, integration, debug

Work closely with firmware and other groups around the globe.