Senior Staff Engineer
Stryker
Gurugram, IN
5d ago

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
  • Report this job
    checkmark

    Thank you for reporting this job!

    Your feedback will help us improve the quality of our services.

    Apply
    My Email
    By clicking on "Continue", I give neuvoo consent to process my data and to send me email alerts, as detailed in neuvoo's Privacy Policy . I may withdraw my consent or unsubscribe at any time.
    Continue
    Application form