Responsibilities
- Ensure that system improvements are successfully implemented and monitored to increase efficiency.
- Designs, develops, troubleshoots, and debugs software programs for enhancements and maximizes new products.
- Determines hardware compatibility and/or influences design.
- Collaborates with cross functional teams to determine customer and product software design requirements.
- Generate systems software engineering policies, standards, and procedures.
- Manages the entire application lifecycle (concept, design, test, release, and support).
- Gather specific requirements and suggest solutions.
- Work with other team members such as Product Owners, QA and process SMEs to assess risk during three project phases (project initiation, pre-validation test assessment and post-validation test assessment)
- Review department specifications and process documentation to ensure compliance with FDA regulations and Medtronic internal quality policies
- Communicate status updates to key stakeholders.
- Candidate must be capable of recognizing factors that could negatively affect project timelines / deliverables and effectively communicate impact to direct manager.
Requirements
- Bachelor of Science degree with Computer Science, Information Technology or equivalent
- Minimum of 4 years of relevant experience, or an advanced degree with a minimum of 2 years relevant experience.
- Strong understanding of backend technologies (e.g., .NET Core, Python, C#)
- Experience using SQL and data modeling to support software solutions.
- French & English fluent
- Ability to travel across EMEA around 20% of your time
Additional Information
- Ability to travel across EMEA around 20% of your time
- French & English fluent
