Raise Your Laboratory Testing Benchmark!

Cecilia Newcomb-Evans, MS

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Cecilia Newcomb-Evans is a highly accomplished research professional with over 37 years of pharmaceutical experience and a proven track record of strategic planning, project execution, laboratory operations and budgeting. Ms. Newcomb-Evans is a technical expert in analytical development who is able to facilitate rapid results and comprehensive outcomes.

A demonstrated leader with a keen ability to design, plan and implement ideas from conception through completion; able to manage multiple responsibilities without compromise to detail or quality; and maintain an overview of ongoing and evolving projects.

Ms. Newcomb-Evans is an experienced communicator who is able to articulate technical information to diverse audiences and build strong working relationships based on accessibility, responsiveness, professionalism and trust.

Ms. Newcomb-Evans has a BS in Chemistry from the University of Illinois at Chicago and a MS in Management from Cardinal Stritch University.

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The Importance of Regular Quality Control Product Testing: How Often is Ideal?

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Regular quality control product testing is a critical aspect of ensuring the overall quality and reliability of products. From electronics to pharmaceuticals, conducting frequent testing helps identify any potential issues or defects early on, preventing costly consequences down the line. But how often should companies perform these tests to strike the right balance between efficiency and effectiveness?

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