Bachelor's degree in software engineering or related field
Three years of relevant engineering experience
Knowledge of fda regulations and quality management systems
The primary purpose of this position is to perform software verification activities related to Software and Firmware areas within the medical device industry
Job Summary
The primary purpose of this position is to perform software verification activities related to Software and Firmware areas within the medical device industry.
You will adhere to strict safety, environmental, security, and quality requirements including U.S. Food and Drug Administration (FDA) regulations.
The role requires collaborating with cross-functional teams to investigate, develop, document, and implement new product and process technologies.
Matching Summary
The primary purpose of this position is to perform software verification activities related to Software and Firmware areas within the medical device industry.
Skills & Requirements
Must-have
Bachelor's degree in Software Engineering or related field
Three years of relevant engineering experience
Knowledge of FDA regulations and Quality Management Systems
Experience with software verification and test plan development
Root cause analysis and failure investigation skills
Nice-to-have
Proactive insight into technical challenges
Strong written and oral communication skills
Ability to work independently with occasional guidance
Positive can-do attitude in high-energy environments
Familiarity with Lean Manufacturing principles
Key Requirements
Bachelor's degree in Software Engineering or related technical field
Minimum three years of relevant experience
Functional understanding of Quality Management Systems (QMS)