Laurel Hoover
Quality Systems Manager@ BIOLYPH
Minneapolis, Minnesota, United States
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Laurel Hoover is a highly experienced professional with 43.6 years of work experience in the Medical Laboratory, Quality, and Regulatory field. She has a strong skill set in technical documentation, flexible, accurate, regulations, data analysis, quality control, immunoassays, project coordination, laboratory skills, organized, standard operating procedures, validation, molecular biotechniques, easily adaptable, quality assurance, and compliance. Laurel has worked in various roles, including Quality Systems Manager at BIOLYPH and Regulatory Affairs Specialist at Zimmer Biomet. She has also worked as a Technical Reviewer and Writer, QC Chemistry Analyst, and Regulatory Assistant at reputable companies. Laurel is based in the United States.
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Emails and Phone Numbers

@biolyph.com
+1 952936****
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About

Professional experience in Medical Laboratory, Quality, and Regulatory. Recent graduate of Molecular Biotechniques lecture and hands-on laboratory program at FAES/NIH in Bethesda, Maryland. Areas of particular interest include Immunology and Molecular Biology.

Work Experience

1317 Fifth Street South, Minneapolis, MN, 55343, US

Biotechnology Research

24
Phone
+1 9529360990
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Laurel Hoover's Professional Milestones

  • Regulatory Affairs Contract Assignment (2003-07-01~2004-05-01): Negotiated and secured multiple contracts, ensuring compliance and maximizing client satisfaction.
  • Quality Assurance Analyst (1997-02-01~1997-07-01): Implementing and implementing robust quality control measures to ensure product excellence and customer satisfaction.
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