Key responsibilities.

• Develop analytical methods that are accurate, precise, and specific for use in both the Quality Control department and the Process Development department. Methods primarily include HPLC and GC but may extend to other testing procedures.
• Document the development of the method in the appropriate notebooks for future reference.
• Prepare PPS-Riverview test methods and supporting documentation for use in the laboratory. 
• Validate analytical methods used in the testing of raw materials, intermediate products, final products, and cleaning samples.  
• Develop validation protocols to assess the necessary features of the test methods.  Assesses all data elements required for assay validation as per the current USP and other regulatory requirements.  Perform protocols as written and documents the results in the form of a comprehensive validation report and makes any necessary changes to existing documents as a result of report findings.
• Assist in the maintenance and calibration of laboratory analytical instrumentation including, but not limited to HPLC and GC. Maintain accurate records regarding the maintenance and calibration activities.
• Support manufacturing operations with testing of raw materials, intermediate products, final products, and cleaning samples. The incumbent is expected to operate in a neat and orderly manner and to provide accurate and timely test results.
• Assist in the maintenance of the QC Laboratory.  In addition to routine housekeeping and glassware cleaning, maintains and appropriate inventory of supplies and chemicals.
• Document sample preparation, equipment set-up and test results in Laboratory Notebooks or on the appropriate test record form.  Documentation must be complete and verified by a second member of the quality group.  In addition, laboratory log sheets, those related to equipment usage, calibration, and maintenance, reference standard inventory, QC chemical inventory, or those related to retention samples will be properly maintained.