·         Conduct routine and non-routine analysis of raw materials, in process, and finished formulations according to standard operating procedures.

·         Perform microbiological and/or 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.