Lauren Bonura

Quality Control Supervisor @ Baebies

About Lauren Bonura

Lauren Bonura is a Quality Control Supervisor with over eight years of experience in the medical device manufacturing industry, specializing in quality assurance and control. She has held various roles in reputable organizations, including LabCorp and Sequenom, and possesses a strong educational background in biology.

Current Role at Baebies

Lauren Bonura serves as the Quality Control Supervisor at Baebies, a position she has held since 2022. In this role, she is responsible for overseeing quality control processes and ensuring compliance with industry standards. Her experience in quality assurance and quality control within the medical device manufacturing industry supports her effectiveness in this position.

Previous Experience at LabCorp

Before joining Baebies, Lauren worked at LabCorp as a Prenatal Genomic Screening Technologist from 2016 to 2018 in Durham, North Carolina. During her two years there, she contributed to the implementation of genomic screening processes and supported laboratory operations.

Professional Background in Laboratory Settings

Lauren has a diverse background in laboratory settings, having worked at Sequenom as a Senior Laboratory Associate from 2014 to 2016 in Morrisville, North Carolina. Additionally, she spent five years as a Laboratory Technician at Environmental Testing Solutions, Inc. from 2005 to 2010 in the Asheville area. This cumulative experience has equipped her with a strong foundation in laboratory practices and quality management.

Educational Qualifications

Lauren holds a Bachelor's degree in Biology from the University of North Carolina at Chapel Hill, where she studied from 2009 to 2013. She also earned an Associate of Science degree from Asheville-Buncombe Technical Community College between 2005 and 2009. Her educational background provides her with a solid understanding of biological sciences relevant to her career.

Skills and Expertise

Lauren possesses over eight years of experience in the medical device manufacturing industry, with a focus on quality assurance and control. She is proficient in working within both GMP and CLIA environments and is skilled in advanced molecular biology laboratory techniques. Her strong attention to detail and problem-solving abilities contribute to her effectiveness in maintaining high-quality standards.

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