The Principal Mechanical Engineer is responsible for design, development, implementation, and analysis of medical devices. Performs engineering design evaluations. May develop a range of products. Recommends alterations to development and design to improve quality of products and/or procedures. Identifies functional problems and suggests resolutions. Complies with applicable quality systems, medical device regulations and pharmaceutical regulations. Works under minimal supervision and is expected to be able to lead the work of other more junior engineers as well as technicians. Coordinates their work with Teva Device Design Centers, Teva Drug-Device Project Teams and manufacturing sites, Contract Development Organization (CDO) or Contract Manufacturing Organization for feasibility, device development and design control activities.
Bachelor of Science in Mechanical or Biomedical Engineering- Required Master Degree- Preferred Pharmaceutical / Medical Device industry experience with extensive experience of developing medical devices- Required Strong presentation and communication skills- Required Ability to work on multiple projects with aggressive timelines- Required Works independently, without daily direction and direct the work of junior group members and prototype technicians- Required Injection Devices- Preferred Speak fluent English- Required The position located in Kfar Saba