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Lisa Saiki

Lisa Saiki

Senior GMP Technical Writer

Pharmaceutical / Bio-tech

Scotts Valley, Santa Cruz

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About Lisa Saiki:

I successfully work as a contract Technical Writer/Senior Validation Contract Consultant with +25 years experience with GMP manufacturing and GDP. Documentation Practices 

Experience

Validation consultant responsible for commissioning and validation of GMP cell therapy manufacturing facility.

Education

I have a B.S. in Biochemistry and Molecular Biology and a B.A. in Legal Studies from U.C. Santa Cruz (1992).

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