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Description:
12 months contract ; Hybrid role ;
Raleigh NC
This is where your work saves lives
As a Senior Principal Software Systems Engineer in the software organization, you will be responsible for developing innovative healthcare solutions and supporting development and sustaining activities within connected Infusion Pump Platforms to meet customer needs and regulatory standards.
What you'll be doing:
Role is Hybrid 3 days in office and 2 from home.
Description:
12 months contract ; Hybrid role ;
Raleigh NC
This is where your work saves lives
As a Senior Principal Software Systems Engineer in the software organization, you will be responsible for developing innovative healthcare solutions and supporting development and sustaining activities within connected Infusion Pump Platforms to meet customer needs and regulatory standards.
What you'll be doing:
- Drive the implementation of best practices in software systems development and product lifecycles in collaboration with development and verification teams, for Digital Applications that are part of infusion pumps ecosystem
- Be a technical leader providing team members guidance and feedback on technical work.
- Develop technical solutions to complex software system problems and deliver high-quality solutions on tight schedules
- Lead efforts with cross-functional team members (e.g. Commercial and Clinical) to document user needs and translate them to user needs into system requirements.
- Lead decomposition of system requirements into software subsystem requirements.
- Lead risk analysis activities for Digital Applications software from the capture of inherent hazards through mitigation implementation.
- Work with verification engineers to define test strategies for the development of verification and validation plans using requirement tracing methods.
- Participate in software design reviews for components or features.
- Perform product backlog and feature grooming/definition activities as part of Agile planning/execution o Drive collaboration with internal and external stakeholders and enable the team on better processes, practices and technical mentorship.
- Interface with manufacturing, service, and customer training staff through the design transfer process.
- Ensure compliance to the product development process and quality system.
- Subject matter expertise in requirements management and risk management for complex, medically regulated, connected/interoperable system of systems
- Bachelor's degree in an engineering discipline with 10 years of experience.
- Experience with Digital Applications (SaMD. MDDS) connected to regulated electro-mechanical devices in a clinical environment preferred.
- Experience with development in an agile environment with experience creating and maintaining product backlogs.
- Excellent oral and written communication skills.
- Experience in a regulated industry preferred.
- Excellent documentation skills.
Role is Hybrid 3 days in office and 2 from home.