Knowledge of fda regulations and quality management systems
The primary purpose of this position is to perform work involving general engineering methods while developing advanced technologies in the medical device industry
Job Summary
The primary purpose of this position is to perform work involving general engineering methods while developing advanced technologies in the medical device industry.
You will adhere to strict safety, environmental, security, and quality requirements including FDA regulations and the company's Quality Management System.
This role requires collaborating with cross-functional teams to investigate, develop, document, and implement new product and process technologies of moderate complexity.
Matching Summary
The primary purpose of this position is to perform work involving general engineering methods while developing advanced technologies in the medical device industry.
Skills & Requirements
Must-have
Bachelor's degree in engineering or related field
Three years of relevant engineering experience
Knowledge of FDA regulations and Quality Management Systems
Ability to perform root cause analysis on failures
Experience with standard engineering techniques and tools
Nice-to-have
Proactive insight into technical challenges
Strong written and oral communication skills
Positive can-do attitude in high energy environments
Familiarity with Integer Production System principles
Experience with 5 Sigma quality journey initiatives
Key Requirements
Bachelor's degree in engineering or related technical field
At least three years of relevant experience
Functional understanding of Quality Management Systems (QMS)