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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.

Required Senior Mechanical Engineer
Description
A fast-growing global medical device company, developing and manufacturing innovative drug delivery and infusion solutions across the continuum of care: from the hospital to the home. As part of our growth and commitment to innovation, we are expanding our R&D department and looking for a Senior Mechanical Engineer to join our Mechanical team in the R&D department. Join us as we continue to grow and make a meaningful impact on healthcare worldwide
Mechanical design and development of multidisciplinary medical devices, primarily infusion pumps and related accessories, with a focus on mechanism development and compact electro-mechanical packaging.
Lead the mechanical aspects of the design and development of new products, from concept through production, while providing ongoing engineering support for the companys existing product portfolio
Direct Manager: Mechanics & HW 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

A fast-growing global medical device company, developing and manufacturing innovative drug delivery and infusion solutions across the continuum of care- from the hospital to the home. We are looking for an excellent Production Manager to join the Operations team.
Job Description:
The Production Manager is responsible for leading manufacturing operations in a regulated medical device environment, managing Production Team Leaders and ensuring efficient, high-quality, and compliant production activities.
Key Responsibilities:
Manage and lead Production Team Leaders, including ongoing professional development, performance management, and support.
Oversee the recruitment, onboarding, and integration of production employees.
Manage workforce allocation and production staffing, including employee assignments and transfers between production stations according to operational needs.
Ensure discipline, adherence to procedures, and high professional standards across the production floor.
Manage, develop, and continuously improve manufacturing and Final testing processes.
Own manufacturing processes and ensure operational quality and compliance.
Ensure production activities are performed in accordance with applicable regulatory requirements, quality standards, and company procedures.
Work closely and collaboratively with the Quality ang Engineering departments to ensure compliance, address quality issues, and continuously improve production processes.
Drive operational excellence and implement Lean methodologies and continuous improvement initiatives
Direct Manager: Director of Manufacturing

A fast-growing international medical device company that develops and manufactures innovative medical equipment. We are looking for a Process Engineer to join our Manufacturing Engineering team.
Job Description:
The Process Engineer will lead engineering changes and qualify manufacturing processes - on our production floor and at our subcontractors in Israel and abroad - while providing hands-on technical support to production.
Lead engineering changes (ECOs) end-to-end, from definition and impact assessment, through implementation on the production floor, to formal closure.
Plan and execute process verification and validation activities, including IQ/OQ/PQ protocols and reports.
Lead process qualification at subcontractors in Israel and abroad, including new and replaced equipment and production lines.
Support injection molding activities: DFM reviews with the molder, mold qualification and evaluation of samples.
Provide hands-on engineering support to production and final test lines, and define jigs, fixtures and process parameters.
Conduct technical investigations and root cause analysis as part of the NCMR process, and drive corrective actions to closure.
Develop, improve and optimize manufacturing and assembly processes, based on production and yield data.
Work closely with Production, Quality, Regulatory, R&D and Purchasing, and manage internal and external stakeholders.
Direct Manager: Engineering Manager.