Description
A leading medical device company, located in Minnesota, is in need of a Sr. Design Quality Engineer to assist with transferring a product development process between sites. The company has been experiencing significant growth due to their innovative products.The Sr. Design Quality Engineer will have the following responsibilities:
- Lead the effort to transfer the risk management files into a new system
- Identify and manage risk throughout the product development process with the use of FMECA
- Contribute to master test plans which encompass design V&V and process validation activities
- Evaluate test protocols and reports to ensure that testing us sufficient to meet regulatory requirements and quality objectives
- Provide input to design and manufacturing documentation
- Contribute to design input requirements
The Sr. Design Quality Engineer must meet the following requirements:
- Bachelors in Science or Engineering (or related field)
- 5-8 years experience in Quality Engineering, R&D Engineering or Process Development Engineering within the medical device industry
- Excellent communication skills
- Ability to work with customers
- Strong understanding of specification development, risk management. design V&V, sterilization validation, and biocompatability testing
- Working knolwedge of electro-mechanical devices and software validation methods
This is a 6 month contract. Please apply now if interested.
To find out more about Real please visit www.realstaffing.com