A world leader in the field of in vitro diagnostics for over 55 years, bioMérieux provides diagnostic solutions which determine the source of disease and contamination to improve patient health and ensure consumer safety.
In North America we have more than 5,000 team members across 11 sites or subsidiaries, including Salt Lake City-based BioFire Diagnostics and one subsidiary in Montreal, Canada.
Come be a part of our team and our mission as a Associate Software Project Manager!
bioMérieux - Salt Lake City is looking for a talented and engaged Software Project Manager to play an integral role in the software development life-cycle for cutting-edge, life-saving medical devices. You will be joining a team that values collaboration, continuous improvement, and a healthy work life balance.
This Associate Software Project Manager will lead a team of software engineers in the research, development, and support of software applications used internally by members of R&D working on molecular diagnostics solutions. They will partner with internal stakeholders in the R&D organization to define inputs for software application development. They will be responsible for writing project documentation and specifications, and working with test engineers to coordinate and execute test plans. They are expected to understand the regulatory requirements regarding medical device software development and cybersecurity, and educate software development teams, as well as other departments, on these requirements. They work to ensure compliance with regulatory requirements and industry best practices. They are expected to foster a collaborative and cooperative environment and develop strategies to drive high quality execution.
Principal Job Duties and Responsibilities -
- Build strong relationships with stakeholders; actively engage to understand their needs
- Prioritize project deliverables and oversee projects from start to finish
- Communicate project risks and status to the larger system development team
- Lead a software development team through all stages of the software development life-cycle
- Be responsible for all aspects of the Quality System requirements for production level medical device software
Qualifications -
- Training and Education: Requires a Bachelor of Science in an engineering, scientific, or technical field.
- Experience: 0+ years of work experience in software development or a related field.
Skills -
Technical Skills:
- Desire to be involved in analysis, design, research, and development
- Basic understanding of the Windows OS
- Basic understanding of source code control, defect tracking and build systems
Writing and communication skills:
- Technical writing experience
- Good verbal communication and presentation abilities
- Attention to detail
- Efficient and creative approach to problem solving
- Good time management with an ability to prioritize projects as needed
