Work Flexibility: Hybrid
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)
Travel Percentage: 20%
Top Skills
What We Do
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 130 million patients annually. More information is available at www.stryker.com.
Together with our customers, we are driven to make healthcare better.
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