Description:
Own design changes and be responsible for the ECNs from end to end.
Manage technical investigations of failures or poor performance issues.
Design, qualify, document and validate: assembly & test fixtures/Jigs and tools, release to production and service.
Evaluate plan and execute cost reduction projects.
Manage EOL cases to minimize risk to production and optimize cost.
Seek new manufacturing technologies to imporove performance and cost.
Manage NPI programs to have successful transition to production.
Construction and management of product DMR including BOM, SOP’s, Mechanical & electrical specs.
Collaborate and communicate with a vast network of global stakeholders.
Requirements:
BSc.in Mechanical Engineering
Minimum of 5 years of relevant experience in Engineering & manufacturing environments
Proven experience of multi-disciplinary products
Fluent in Hebrew and English
Advantage:
Experience in Medical Device companies or other highly regulated industries
Understanding and knowledge of relevant regulations and standards FDA QSR, ISO 13485, ISO 14971, MDD-significent advantege
Master degree (in a relevant field)
Experience with design of surgical tools
Solidworks expertise