Software Validation Engineer II
hace 5 días
Transforming Lives through Medical Technology
About the Role
We are seeking a highly skilled Software Validation Engineer II to join our team at Medtronic. As a key member of our engineering team, you will be responsible for ensuring the quality and reliability of our software applications and systems.
Key Responsibilities
- Design, develop, execute, document, and implement all validations related to software.
- Knowledge of manufacturing equipment software, PLC, HMI, etc.
- Test the functionality and performance of software applications or systems software.
- Ensure software applications or systems software meet technical and functional requirements.
- Troubleshoot software/equipment malfunctions.
- Write/execute Process Validation Protocols (Software, IQ, OQ, PQ).
- Create/execute Engineering Changes Orders.
- Write/approve changes related to manufacturing documentation such as Manufacturing Work Instructions, BOM, etc.
Requirements
- Bachelor's degree in industrial engineering or a related field.
- 2-3 years of relevant experience.
- Experience in medical devices, ISO 13485.
- Software validation expertise.
Preferred Qualifications
- Experience with software validation in a medical device industry.
- Knowledge of regulatory requirements for software validation.
What We Offer
At Medtronic, we offer a dynamic and supportive work environment that fosters growth and development. We are committed to helping our employees achieve their career goals and providing opportunities for advancement.
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