Validation Engineer

Minneapolis  ‐ Onsite
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Description

Validation Engineer - 6 Month Contract - Medical Device - Minneapolis

My client, one of the top Medical Device companies globally, has an exciting Quality Engineering opportunity. They are looking for a motivated individual who has a strong background in Validation and Test Method Development. This is a great opportunity to work on cutting edge Medical Device products.

Responsibilities
  • Process qualification
  • Review IQ/OQ/PQ documents from manufacturing counterparts
  • Develop test method development and validation protocols to establish acceptance criteria as well as write reports
  • Determine if data sets meet acceptance criteria
  • Participate in cross functional teams
  • Implement and conduct data analysis, system evaluation and product assessment to ensure finished products meet standards
  • Ensure compliance to ISO 13485 and 21 CFR 820


Requirements
  • Bachelors in an Engineering field
  • Medical device experience
  • Strong understanding of Process Validation (IQ/OQ/PQ) - must be able to define this and say why companies do this
  • Self starter
  • Independent
  • Open communicator


If you, or anyone you know are interested, please get in contact with me as soon as possible via email, as all first round interviews will be confirmed by the end of this week!

For Immediate consideration please apply online or contact Jack Feeley at
Start date
07/2014
Duration
6 Months
From
Real Staffing
Published at
09.07.2014
Project ID:
738740
Contract type
Freelance
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