Ryan Thurber Email & Phone Number

Chanhassen, Mn

Develop and validate analytical methods (HPLC, ICP-OES).Hire and train new department staff.Troubleshoot and maintain the calibrated status of laboratory equipment.

Chaska, Minnesota, United States

Supervised the handling and storage of customer-supplied raw materials.Responsible for compounding formulas based on customer requirements.

New Hope, Mn

• Successfully developed and validated new HPLC analytical procedures• Conducted experiments designed to determine the root-cause of product-related problems• Interpret data and adhere to strict project related timelines• Identified and improved “troublesome” existing HPLC/UPLC analytical procedures resulting in greater efficiency and fewer procedural errors• Advise management and coworkers in the areas of product stability, routine testing and cleaning validation analysis• Responsible for writing, executing and concluding technical protocols• Earned a reputation as a hard worker and a go-to person for technical questions and advice• Facilitated method transfers to Quality Control from Product Development • Successfully trained laboratory staff regarding analytical procedures and new laboratory instrumentation• Performed review of analytical data and documentation for FDA compliance• Gained operational knowledge of other analytical instrumentation, such as GC, UV-vis and particle size determination • Perform physical and chemical tests based on new and existing procedures• Analyze excipients and active pharmaceutical ingredients from various sources to determine appropriateness for use in new products

•Successfully submitted Abbreviated New Drug Applications (ANDA) to the FDA for manufacturing and sales approval•Perform method verification of compendial procedures•Perform routine maintenance and calibration of laboratory instruments•Interface with co-workers, supervisors, and corporate officers to communicate results through appropriate documentation, statistical analysis and trending•Perform all quality control analytical methods as required•Accurately document all data per cGMP requirements•Perform investigations and authored reports for any deviations from acceptable product specifications•Gained working knowledge and troubleshooting skills of HPLC, UV-vis and dissolution