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 you to investigate, develop, document, and implement new product and process technologies of moderate complexity while supporting Manufacturing Excellence strategies.
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 work independently with occasional guidance
Strong written and oral communication skills
Nice-to-have
Positive can-do attitude in high energy environment
Experience with continuous improvement methodologies
Understanding of Integer Production System principles
Proactive insight into technical challenges
Collaborative team player with cross-functional experience
Key Requirements
Bachelor's degree in engineering or related technical field
Minimum three years of relevant experience
Functional understanding of Quality Management Systems