Christie Kunde, Pharmd Email & Phone Number

Phoenix, Arizona, United States

Helping you make informed drug choices based on your DNA

Tempe, Arizona, United States

Conducted daily audits of Medicare coverage determinations and redeterminations to ensure regulatory compliance and audit readiness.• Improved quality and reduced audit risk by presenting process improvement ideas through regular meetings with internal teams and participating in special projects and assignments.• Implemented procedure for auditing redetermination requests resulting in decreased errors and enhanced clinical decision making.• Developed and presented multiple training materials to various departments to increase consistency and CMS compliance.• Acted as a resource for compliance and clinical matters during the CMS program audit, internal mock audits, team meetings and as needed by colleagues.

Nashville, Tennessee, United States

Reviewed Medicare Part D prior authorization requests using established criteria and provided customer service over the phone to patients, pharmacies and clinicians regarding, but not limited to, co-pay information, plan design, medication alternatives and prior authorization decisions. • Audited prior authorizations requests of fellow technicians leading to increased compliance of CMS regulations.

Torrance, California, United States

• Performed analysis on raw materials and water samples for the quality control department of a pharmaceutical company that specializes in peptide synthesis• Maintained appropriate documentation as required by Current Good Manufacturing Practice (CGMP)• Responsible for operation, preventative maintenance, and calibration of analytical instruments• Accountable for complying with all state and federal laws including the Food and Drug Administration (FDA) and Occupational Safety and Health Administration (OSHA)

Garden Grove, California, United States

• Worked for a large nutraceutical company as a quality control chemist performing high-performance liquid chromatography (HPLC) analysis and documentation of finished products, stability and validation lots, research and development samples, and raw materials• Prepared and maintained reagents, standards, and samples• Readied HPLC by preparing mobile phase and performing routine maintenance and calibration of equipment • Supported development and validation of methods through the testing of samples• Maintained and assured compliance to CGMP, OSHA, FDA, and all other agency regulations as applicable

Pharmd, Pharmacy

Mba, Healthcare Management

Bachelor, Chemistry

Diploma, General Studies