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We are looking for a motivated and detail-oriented Junior Mechanical Designer to join our growing engineering team. This is a great opportunity for someone at the beginning of their career who is passionate about product design, mechanical systems, and turning ideas into real-world solutions.
You will work closely with senior engineers, product teams, and manufacturing partners to support the design and development process from concept to production.
Responsibilities:
Assist in the design and development of mechanical components and assemblies
Create and update 2D drawings and 3D CAD models
Support prototype development and product testing
Prepare technical documentation and manufacturing files
Collaborate with engineering and production teams to ensure design accuracy
Participate in design reviews and problem-solving discussions
Help maintain engineering standards and documentation consistency

In this hybrid role, this individual will manage and direct all West IL planning activities including subcon sites planning, OTIF and cutomers related issues. The role include all export shipments monitoring and partnering with West logistics providers on a daily basis. Planning mgr will set working processes and enhance improvments and will play a key pivotal role in our supply chain department

Essential Duties and Responsibilities
Develops and implements policies and procedures for production operations
Plans, examines, analyzes, and evaluates production operations
Manage Supply Chain KPIs as OTIF,OTD, Subcon performance and lead Suppliers QBRs meetings
Establish and maintain long term capacity model
Prepares planning and production reports, reviews operating and financial data and makes recommendations for improvements
Adress planning issues and be supply chain point of contact for customer complaints
Act as the Supply Chain focal point for for all NPI/ECOs issues and plan ahead acitvities with QA/RA/Eng/RD

DRS RADA, a leading defense high-tech company specializing in radar systems development, is seeking a motivated and skilled PMO to join our R&D department. Responsibilities:
* Provide operational support for all R&D projects, assisting in the execution of work plans.
* Track annual work plans, ensuring alignment with objectives, monitoring progress against plans, managing resources, and identifying risks.
* Work extensively with the company’s project management systems to maintain project control.
* Work extensively with the factory for resource coordination and major breakdowns.
* Oversee project timelines and proactively manage risks to ensure project milestones are met.
* Assist development teams with procurement and logistics processes.
* Collaborate closely with R&D team leaders, project managers, system engineers, procurement teams, and production staff.
* Active involvement in the project life cycle (KOM, DRs, installation, integration, validation).
* Align/focus the project team towards the main goals.
* Responsibility for coordinating and managing subcontractor activities, mainly timelines, compliance, terms, and financials.

we are 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 our companys 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.