Description
The Quality Engineer will have the following responsibilities:- Write protocols and implement validation plans
- Coordinate new process techniques that improve overall job efficiencies
- Implement systems and procedures that assure compliance with quality standards
- CAPA related to supplier performance
- Provide engineering team with data from analysis tools as needed
- Work cross functionally with quality assurance, manufacturing and engineering
The Quality Engineer must meet the following requirements:
- Medical device assembly experience
- Strong understanding of validation processes (IQ,OQ,PQ)
- Strong auditing experience
- Excellent understanding of ISO standards
- Experience with sterilization processes, validation and ongoing production management of the supplier
- Strong communication skills
- Excellent problem solving capabilities
To find out more about Real please visit www.realstaffing.com