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Instructors
Sandra Storli

Education

MS in Regulatory Affairs (in progress)
Purdue University
West Lafayette, IN

MBA in International Business
Franklin University
Columbus, OH

MS in Food Science and Nutrition
University of Wisconsin-Stout
Menomonie, WI

BS in Dietetics
Minor in Chemistry
Minor in Biology
Minor in Food technology
University of Wisconsin-Stout
Menomonie, WI

Languages

  • English

Sandra Storli

CBA, CHA, CMQ/OE, CQA

Education

MS in Regulatory Affairs (in progress)
Purdue University
West Lafayette, IN

MBA in International Business
Franklin University
Columbus, OH

MS in Food Science and Nutrition
University of Wisconsin-Stout
Menomonie, WI

BS in Dietetics
Minor in Chemistry
Minor in Biology
Minor in Food technology
University of Wisconsin-Stout
Menomonie, WI

Languages

  • English

Professional Experience

Sandra Storli offers 30 years of experience working with corporate organizations in quality and regulatory compliance. She is currently a regional counselor for the Food, Drug, & Cosmetic Division, membership chair of the local ASQ section 1212, and works with the ASQ Learning Offerings workgroup teaching the Certified Quality Auditor (CQA) auditing class. Sandy has held various managerial, supervisory, project management, and individual contributor positions with Abbott, Kellogg Company, and Zimmer Biomet. She is a reviewer for "The ASQ Auditing Handbook and The Certified Pharmaceutical GMP Professional Handbook," has written two technical articles, and has co-authored the technical standard, “Best Practices for Biomedical Research in Drug Development.”

Sandy has worked with several of ASQ divisions in promoting quality as a regional counselor for Region 12 for the Quality Management Division, Audit Division, Healthcare Division, and Food, Drug, & Cosmetic Division. She is also a member of the Technical Program Committee (TPC) for the ASQ World Conference on Quality and Improvement. She works with several conference speakers reviewing and assisting them with their presentation material.

A highly motivated individual, Sandy takes initiative to improve global quality management systems to meet future business challenges in medical devices, diagnostics, and pharmaceutical and biotechnology sectors. She has expertise in training, auditing, compliance, negotiation, problem solving, time management, oral and written communication, and prioritizing multiple projects, as well as a proven track record of success in aligning goals to drive process improvement and productivity using limited resources. She has extensive international quality experience that includes Asia, EMEA, and South America.