Validation Engineer

A Medical Device company is in need of a Process Validation Engineer to assist with validation of new product lines. The company, located in Minnesota, is focused on developing and manufacturing a diverse portfolio of high quality medical products. The Process Validation Engineer will have the following responsibilities:- Work with engineers to develop, document, and execute validation lifecycle documentation- Work cross functionally with Quality to ensure Process, Equipment, and Software requirements, validation plans, tests, and reports are consistent- Support Validation maintenance The Process Validation Engineer must meet the following requirements:- B.S Engineering or Life Sciences field- Minimum of 4 years experience in Medical Device industry with an emphasis on process validation- Strong understanding of GMP requirements and 21 CFR 820- Ability to work cross functionally with various groups- Strong communicator- Team oriented This is a 6 month contract, $45-$40/hour. If you are interested please apply now!

To find out more about Real please visit www.realstaffing.com [1]

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[1] http://www.realstaffing.com