• Conduct routine and non-routine HPLC/GC analysis of raw materials, in process, and finished formulations according to standard operating procedures.
• Perform chemical analyses of product to ensure stability.
• Compile data for documentation of test procedures that may include microbiological and/or chemical assays, stability program testing and formulation studies.
• Calibrate and maintain lab equipment.
• Participate in the preparation of investigations, summaries and reports.
• May assist in developing testing methods.
• Review data obtained for compliance to specifications and report abnormalities.
• Revise and update standard operating procedures as needed. 
• May perform special projects on analytical and instrument problem solving. 
• Applies knowledge of good manufacturing practices, good laboratory practices and good record keeping practices on a daily basis.
• Follows written test methods and protocols. 
• Process data, report data and prepare tables and graphs for the completed testing. Identify problems, e.g. out of trend data. Professional interactions are primarily within the QC organization.
• Responsible for observing all Company, Health, Safety and Environmental guidelines.

Job Summary