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    <pubDate>Wed, 19 Jun 2013 15:17:19 GMT</pubDate>
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      <title>Manufacturing Engineer - Validation</title>
      <description>CO-Monument, As an experienced Manufacturing Engineer within the Medical Device industry, the engineer will be providing guidance and conduct remediation activities related to Process Validation. 5+ years validation experience Test Method, Equipment, and Process Validation experience Experience writing and executing protocols including IQ,OQ,PQ,PPQ FDA regulated experience Has a good holistic understanding of </description>
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      <pubDate>Tue, 18 Jun 2013 08:22:13 GMT</pubDate>
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      <title>Manufacturing Engineer Validation</title>
      <description>PA-West Chester, As an experienced Manufacturing Engineer within the Medical Device industry, the engineer will be providing guidance and conduct remediation activities related to Process Validation. 5+ years validation experience Test Method, Equipment, and Process Validation experience Experience writing and executing protocols including IQ,OQ,PQ,PPQ FDA regulated experience Has a good holistic understanding of </description>
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      <pubDate>Tue, 18 Jun 2013 08:23:28 GMT</pubDate>
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      <title>Validation Master Plan Developer</title>
      <description>TX-College Station, · Validation Master Plan development for a "Retrofit" C&amp;Q Project at a sterile vaccine manufacturer. · Facility was originally commissioned without cGMP. Objective is to C&amp;Q "legacy" equipment. · Equipment is 2-3 yea Write Strategy and Methodology document for Equipment Qualification Protocols for pre-existing aseptic processing and Extremely strong working knowledge and experience with sterile fa</description>
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      <pubDate>Tue, 18 Jun 2013 00:13:43 GMT</pubDate>
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