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      <title>Supervisor, Quality Control</title>
      <description>OH-Wilmington, The Quality Control Chemistry Supervisor leads groups of chemists to perform testing to meet QC cycle times and to comply with all Alkermes criteria and cGMP's. The Supervisor works cross-functionally with QC management and leaders of other departments to support the commercial release of raw materials and finished products. KEY DUTIES: Oversee training program for direct reports. Assist with trou</description>
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      <pubDate>Fri, 24 May 2013 08:15:39 GMT</pubDate>
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      <title>Quality Control Analyst II/III</title>
      <description>OH-Wilmington, Job Description: Perform routine/non-routine physical, chemical, and in-vitro assays of clinical, commercial, stability, process and cleaning validation samples, and process development samples to support Manufacturing. Participates in the preparation of investigations, summaries and reports. Reviews data obtained for compliance to specifications and reports abnormalities. Revises and updates stan</description>
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      <pubDate>Fri, 24 May 2013 08:30:10 GMT</pubDate>
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      <title>Quality Associate III</title>
      <description>OH-Wilmington, GENERAL DESCRIPTION: This function is responsible for supporting the daily manufacturing and facility operations. Functions include discrepancy resolution, document review, training program support, batch record review, and project management. This function partners with manufacturing to identify resolution to events in consultation with Quality Management. The position will support completing tas</description>
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      <pubDate>Fri, 24 May 2013 08:37:14 GMT</pubDate>
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      <title>Quality Associate III</title>
      <description>OH-Wilmington, GENERAL DESCRIPTION: This function is responsible for supporting the daily manufacturing and facility operations. Functions include discrepancy resolution, document review, training program support, batch record review, and project management. This function partners with manufacturing to identify resolution to events in consultation with Quality Management. The position will support completing tas</description>
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      <pubDate>Thu, 23 May 2013 00:16:20 GMT</pubDate>
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