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
Who we want :
Detail-oriented process improvers. Critical thinkers who naturally see opportunities to develop and optimize work processes finding ways to simplify, standardize and automate.
Self-directed imitators. People who take ownership of their work and need no prompting to drive productivity, change, and outcomes.
Analytical problem solvers. People who go beyond just fixing to identify root causes, evaluate optimal solutions, and recommend comprehensive upgrades to prevent future issues.
Goal-oriented developers. Keeping the customer and requirements squarely in focus, people who deliver safe and robust solutions.
Delivers results. A driven player who sets high goals for personal achievement and organizational success. He / she measures success against the best internal and external benchmarks
What you will do :
Design and implement complex software components and subsystems including object-oriented analysis and design, drafting design documentation, and planning and conducting integrations and component tests.
Support the design of the architectural concepts and basic framework of the product.
Develop expert knowledge within the team of regulatory standards applicable to medical device and software development life cycle : ISO 13485, ISO 14971, and IEC 62304.
Ensure a smooth transition from the product’s concept phase to maturity phase.
Provide technical solutions to complex problems.
Follow the company’s quality process and complies with quality management system procedures.
Participate in software planning and estimating activities.
Attends and supports engineering and surgeon review labs.
What you need :
Experience working in a regulated industry : Medical, Aerospace, etc.
Bachelor or master’s degree in computer science. Master’s degree is preferred.
Minimum 7+ years of experience in design and development.
Highly skilled in C++, OOPS, Object oriented design and analysis, Multithreading (POSIX).
Knowledge of IPC over Linux
Expert level knowledge in data structures.
Use of software developments tools, such as compilers, interpreters, programming editors, debuggers, source code control, defect management.
Demonstrated communication and documentation skills.
Knowledge of Embedded system is a big plus.
Must be able and flexible to work well under changing priorities in a high energy and demanding environment.
Strong communication, analytical, and problem-solving skills.
Goal oriented with strong sense of responsibility and team player.
Demonstrated knowledge of regulatory standards and quality processes will be good to have