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Why join Stryker?
Looking for a place that values your unique talents? Discover Stryker's award-winning culture.
We are proud to offer you our total rewards package which includes bonuses, healthcare, insurance benefits, retirement programs, wellness programs, as well as service and performance awards – not to mention various social and recreational activities, all of which are location specific.
Job description
Who we want:
Dedicated achievers. People who thrive in a fast-paced environment and will stop at nothing to ensure a project is complete and meets regulations and expectations.
Curious learners. People who seek out cutting-edge research and information to expand and enhance their ability to be ready for what’s next.
Self-directed initiators. People who take ownership of their work and need no prompting to drive productivity, change, and outcome and will stop at nothing to ensure a project is complete and meets regulations and expectations
Champions talent development. A developer who focuses on maximizing the ability, potential and contributions of themselves and others.
What you will do:
Technical Responsibilities:
• Assist with prototyping and bench testing
• Support problem solving, identify potential solutions, and evaluate them against requirements
• Under supervision, conduct research and studies to support product design
• Code development time/resource estimation to support projects
• Generate and review the necessary documents with project teams (requirements/design/architecture/bugs/test)
Business Responsibilities:
• Interpret customer needs and understands design inputs
• Understand the product’s intended use and clinical procedures
Med Device Compliance:
• Understand fundamental industry standards, design requirements and test strategies that align with regulatory requirements
• With supervision, create or refine engineering documentation, such as the Design History file per company design control procedures
• Learn R&D procedures like design controls and risk management, per the Quality Management System
General Responsibilities:
• Work cooperatively with R&D, Quality, Manufacturing, Regulatory, Clinical, Marketing and Project Management to ensure project success and contribute to the project as a team member
• Learn procedures, policies, processes, systems, and technology required
• Work on problems in limited scope; purposefully learn while gaining experience
• Design, develop, modify, evaluate and verify software components for medical devices
• In code reviews apply design principles, coding standards and best practices
• Demonstrate ownership and integrity of work
• Build stable relationships
• Participate in code reviews applying design principles, coding standards and best practices
Minimum Qualifications (Required):
• Bachelor's degree in Software Engineering/ Computer Science or related discipline & 3+ years of work experience
• At least 2+ years of hands-on experience in C++ and Qt.
Preferred Qualifications (Strongly desired):
Technical Skills:
• Exposure to programming skills
• Good knowledge on design pattern, WEB API, SQL and Database, Cloud Technologies (MS Azure, Amazon).
Design and Development Skills:
• Experience with integrated development environments (IDE) for projects
• Experience with tools for static/dynamic analysis, memory management, code coverage and techniques for analyzing software
• Integration and deployment processes
Software Process Skills:
• Software Development Life Cycle processes
• Application Lifecycle Management /Traceability tools
• Regulatory and compliance standards applied to the SDLC (Software Development Life Cycle)