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Job Details
Why engineering at Stryker? At Stryker we are dedicated to improving lives, with a passion for researching and developing new medical device products. As an engineer at Stryker, you will be proud of the work that you will be doing, using cutting-edge technologies to make healthcare better. Here, you will work in a supportive culture with other incredibly talented and intelligent people, creating industry-leading medical technology products. You will also have growth opportunities as we have a culture that supports your personal and professional development. Need another reason to apply? Check out these 8 reasons to join Stryker's engineering team: https://www.strykercareersblog.com/post/8-reasons-to-join-strykers-engineering-team Welcome to join the Stryker/Jolife AB team in Lund where we develop and manufacture the LUCAS chest compression system; a life-saving medical device invented in Lund and used by emergency care professionals all over the world to treat sudden cardiac arrest patients. The System Engineer will be part of shaping the future for circulatory treatments and to promote product innovation This role operates within an international environment characterized by regulatory requirements and working in close collaboration with other departments including RAQAC, Operations and Marketing. The System Engineer will provide leadership for products and projects that involve multi-disciplinary engineering teams. You will be involved in all aspects of a product lifecycle from Concept through Market Release and Sustaining. Opportunities & benefits that the role offers
- This person will be exposed to our passion to develop emergency care solutions that are designed to help save lives.
- Opportunity to work on fulfilling projects with local and international colleagues within the department as well as cross functionally.
- Help shape the future of the LUCAS device to ensure we provide best in class products to our customers.
- Work in Europe’s 6th best “Great Place to Work”.
- Attractive flexibility in working arrangements.
- You will coordinate the system development by owning requirements and ensuring that the device system fulfills the requirements.
- Ensure that the design meets user needs through requirements identification, decomposition, verifications and validations.
- Develop, review, and approve Design Control documentation.
- Execute activities for system integration and may lead the Verification effort.
- Interpret and apply governmental regulations, agency guidelines, and internal procedures to assure compliance, and assist the organization in driving implementation.
- Ensure new system development meet user needs as well as regulatory requirements and customer quality expectations.
- Collaborate with global R&D authorities through direct engagement on matters related to system development.
About the Company
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers... Read more