Medtronic Visionsense is Hiring!rabota_il — 06.08.2018 Location: Petah Tikva
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Manufacturing Engineer will work as a team member with the Operation Manufacturing team, Quality and R&D organizations to ensure the successful transfer and ongoing production of finished goods Medical Devices at Medtronic Contract Manufacturing sites. Applicant must demonstrate the ability to deliver good communication, quality, innovative, manufacturability, cost-effective and timely solutions in a multiple project environment.
Senior Supplier Quality Engineer
The Senior Quality Engineer is responsible for managing finished goods Contract Manufactured (CM) for MS- MITG.
Primary duties are focused on all QMS related matters pertaining to selection, qualification, manufacturing, QMS development, and technical quality/service/costs improvements.
Senior Sustaining Engineer
The Senior Sustaining Engineer will be responsible for new product development transfer to manufacturing and ongoing sustaining support of Medtronic Products. He will work as a team member with the Mfg., Quality and R&D to ensure the successful transfer and ongoing production of Medical Devices. Applicant must demonstrate mechanical and technical ability to deliver quality, innovative, and timely solutions in a multiple project environment.
The NPI Engineer will be a contributing member of R&D team that responsible for product development. He will be responsible to complete all the advance manufacturing deliverable for a program to develop and launch the manufacturing process.
Hardware Electrical Engineer
The Hardware Electrical Engineer will be a contributing member of R&D team that responsible for product development, Design, Development and testing of various hardware products including cards, cables and sub-systems.
Senior Software Engineer
The Senior Software Engineer will be a contributing member of R&D team that responsible for product development.
Take a major part of the design, development, testing and delivery of all software products of the company.
Software and System QA Engineer
The Software and System QA Engineer will be a contributing member of R&D team that responsible for product development.
Take a major part of the design, documentation and testing of all software products quality related tasks of the company.
Senior Mechanical Engineer
The Senior Mechanical Engineer will be a contributing member of R&D team that is responsible for product development. He will be responsible for the development of new Medical products in the Endoscopy visualization field.
Regulatory Affairs Specialist
The Regulatory Affairs Specialist will Provide worldwide regulatory affairs support by accomplishing activities that lead to, and maintain global regulatory approvals. Responsible for assessment of device changes for regulatory implications and for performing regulatory activities in support of implanting these device changes. Ensure Medtronic compliance with applicable regulations for the projects, products and tasks allocated. This position typically reports to the Regulatory Affairs Manager. This person will be part of our Surgical Innovations division and work on innovative imaging solutions.
Regulatory Affairs Manager
The Regulatory Affairs Manager will Provide direction and leadership to a team of Regulatory Affairs Specialists in the development and implementation of global regulatory strategies and processes to assure timely global commercialization of products in compliance with applicable regulations and standards. Provide management support to submissions, regulatory activities and supervise/drives the preparation of deliverables to introduce new/ changed products to global markets. Often lead the regulatory support for new and existing products and implement worldwide regulatory plans. Ensure Medtronic compliance with applicable regulations for the projects, products and tasks allocated. This person will be part of our Surgical Innovations division and work on innovative imaging solutions.
Quality Assurance Positions
Quality System Specialist
Quality Systems Specialist will develop and maintain site quality system, processes and procedures to ensure compliance to regulatory and Medtronic corporate requirements. provide quality system guidance and process improvements collaborating with different functions and ensure they are effectively documented, implemented and maintained.
Review and approve quality system document changes. Develop, maintain, and communicate metrics related to the quality system.
Complaints handling Quality Specialist
The Complaints handling Quality Specialist will Review, evaluate and ensure complaint files are complete and maintained properly to satisfactorily meet Quality System Regulations requirements.
Follow company policies and site procedures to ensure that complaint handling activities comply with the appropriate regulations. Write Investigation Summaries based on technical product analysis information.
Design Quality Engineer - Risk Specialist
The Design Quality Engineer - Risk Specialist will Design Quality Engineer will provide technical quality engineering expertise which leads to the development and introduction into production of safe and reliable medical device products.
The Design Quality Engineer will function as the design for safety and reliability representative on cross functional product development teams and will be responsible for facilitating product safety risk management and reliability planning while ensuring compliance to the applicable regulations and standards.
New Product Development Supplier Quality Engineer
The NPD-SQE New Product Development Supplier Quality Engineer is responsible for driving exceptional part quality through his/her expertise in supplier selection strategy, supplier development, and part qualification. This role assists new product development teams and suppliers in providing parts that consistently meet quality, delivery, and cost requirements. Success requires broad knowledge of manufacturing methodologies, design control systems, and quality management practices.
New Product Senior Quality Assurance Engineer
The New Product Senior Quality Assurance Engineer contributes to and leads all aspects of quality related to development and introduction of new products/processes responsible for medical device safety risk management, quality planning in new product development, product/process reliability program management, supplier product/process introduction or improvement, production trouble shooting, or individual measurement and analysis projects.
performing measurements, creating engineering designs, developing plans and keeping design files on all projects; Functioning as a member of cross functional teams by providing technical expertise for projects or subprojects.
Software Quality Engineer
The Software Quality Engineer position is responsible for various software quality assurance functions during the development lifecycle of medical devices. This position shall be responsible for the verification testing of medical device software. In addition, the position is responsible for advancing best practices and ensuring that the software development process is followed. This includes identifying and mitigating risks appropriately. This individual will support the development of documentation required for FDA and MDD device approval. The individual will work as a principle member of new product development team.