Kristine Marino
Clinical Quality Assurance Consultant@ RegDev, Inc.
Modesto, California, United States
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Kristine Marino is a highly experienced professional with 22.9 years of work experience in the pharmaceutical/biotech industry. She has a strong background in GMP, quality assurance, capa, software documentation, and FDA regulations. Kristine has worked in various roles, including Associate Director of Clinical Quality Assurance at BeiGene and Associate Director of Quality Assurance at Parker Institute for Cancer Immunotherapy. She has also served as a Senior Clinical Quality Assurance Operations Specialist at Medivation and as a QA Compliance Officer at the FDA. Kristine's expertise and extensive work history make her a valuable asset in the field of quality assurance.
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Emails and Phone Numbers

@gmail.com
@medivation.com
@parkerici.org
@regdevinc.com
@celgene.com
+1 508521****
+1 617445****
+1 617536****
+1 415652****
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About

17 years varied GXP experience in the pharmaceutical/biotech industry. 2 years experience consulting in a company under consent decree. 14 years experience in Quality Assurance. 7 years experience supporting marketed pharmaceutical/ biologic products. 2 years experience in QA compliance role for Clinical IVRS Software Company Training in International cGMPS. Audit experience includes, FDA; CDER/CBER, EMEA, KFDA, and Due Diligence.

Work Experience

37
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Kristine Marino's Professional Milestones

  • Associate Director Quality Assurance (2017-08-01~2018-03-01): Implementing rigorous quality control measures to promote and maintain adherence to industry standards and standards.
  • Qa Compliance Specialist Ii (2004-01-01~2008-01-01): Improving product quality through thorough inspections and rigorous testing processes.
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Education

Bradford College
Bradford College

Liberal Arts,

Liberal Studies,

Bachelors,

Bachelor Of Arts

1991-1994