Karen Zimm currently is a Manager in Global Regulatory Affairs - Post Approval CMC at Johnson & Johnson Pharmaceutical Research & Development. Previously she has held positions in Technical Operations with Pharmaceutical Sourcing Group - Americas (a division of Ortho-McNeil Pharmaceutical - J&J), in Formulation Development for the R.W. Johnson Pharmaceutical Research Institute (J&J) and Wyeth Consumer Products (Whitehall Robins Healthcare), a division of Wyeth. She earned a BS in Pharmacy and PhD in Pharmaceutics from the Philadelphia College of Pharmacy and Science, a MS in QA/RA from Temple, and most recently an MBA in Pharmaceutical Management from Drexel University. She enjoys instructing classes in an interactive and dynamic style, noting that the knowledge and professional experience of the QA/RA students contribute greatly to the overall learning experience.

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