לוח משרות דרושים ייצור ותעשייה ברמת גן, לחיפוש זה נמצאו 132 משרות

Hands-on mechanical engineering on a defense-tech R&D team. You'll own the mechanical design of subsystems and mechanisms, working under the Mechanical Engineering team lead, design fast, manufacture fast, fail fast, and reiterate fast. The team is small and growing; you'll have real ownership from day one.
Responsibilities:

* Own the mechanical design of assigned subsystems and mechanisms, working under the team lead 's architectural direction.
* Run structural, thermal, vibration, and shock FEA on flight-critical or fire-critical components.
* Drive DFM/DFA and work directly with subcontractors, machine shops, and suppliers.
* Partner with system, electrical, software, and V&V teams on integration.
* Plan and execute qualification TEST campaigns through to acceptance.
* Contribute to design reviews and help mature the team's engineering practices.

We are looking for an experienced Senior Missile control engineer to join our advanced defense-tech R&D team. The role involves leading the development, integration, and testing of missile control systems throughout the full system lifecycle, from algorithm design through simulation, hardware-in-the-loop testing, and flight trials.
Why Join us?:
This is a unique opportunity to be at the heart of a defense-tech startup during its most exciting growth phase!
Responsibilities:

* Lead the design, development, and analysis of missile control algorithms.
* Perform simulations, performance analysis, and robustness assessments.
* Identify technical risks and propose practical engineering solutions.
* Collaborate closely with systems engineering, software development, aerodynamics, mechanical design, and testing teams.
* Participate in and analyse field experiments.
* Ensure compliance with relevant engineering standards and safety requirements.

How you will make an impact:
Perform visual, dimensional, and functional inspection across all components using a wide variety of all applicable tools and equipment such as magnifying lamp, microscope, ensure conformance with design specifications.

Working independently at the highest levels of productivity.

Perform in process and final functional testing of medical device products.

Review, follow and perform job functions in compliance with established work instructions and adherence with SOPs, including recording traceable information on device history records and may enter information into electronic applicable system.

Perform verification of manufacturing documents with component and device drawings, which may include Geometric Dimensioning and Tolerancing methodologies.

May control inventory to ensure appropriate storage conditions and movement.

How you will make an impact:

Lead and oversee Quality Management System (QMS) activities at the Edwards - Innovalve, including NCR, MRB, and CAPA.

Partner and collaborate with Operations, R&D and to align and prioritize activities and to address quality issues.

Manage and mentor the sub-functions of Quality Control.

This role offers an exciting opportunity to contribute to the development of innovative delivery systems and support clinical investigations and complaint handling, partnering with QA and Clinical Development that will revolutionize the treatment of cardiovascular diseases.

How you will make an impact: 

As an R&D Engineer, Provides expertise in the optimization of product development for the Innovalve delivery system and accessories.

Design and Development: Design, analyze, and develop components and processes that meet stringent quality, performance, and regulatory requirements.

Problem-Solving: Identify and troubleshoot complex technical issues that arise during development and clinical trials.

Custom Solutions: Develop tailored solutions for unique design challenges and clinical requirements

Lead and perform product investigations for returned products and complaint samples, including hands-on functional evaluation, data collection and custom testing setup development.

Analyze investigation data to determine probable root cause and contributing factors using structured problem-solving methods (e.g., 5-Why, Fishbone).

Prepare clear technical summary reports and present investigation results to cross-functional teams; track actions to closure.

Work closely with Quality Assurance to support complaint handling workflows, ensure investigation documentation is complete, and align on conclusions and next steps.

Follow up on complaints arising from clinical cases (e.g., case questions, device performance observations) and provide timely technical input to R&D, QA and Clinical Development teams.

Collaborate with cross-functional partners to define and implement corrective actions addressing issues identified through investigations.

Support change management activities (e.g., ECOs) and contribute to risk management updates as needed based on investigation learnings.

Clinical procedure experience - Advantage.