Lonza
Laura LeClair is an experienced QA Manager in Cell Therapy Operations at Lonza, with a career spanning from September 2008 to the present, where responsibility includes ensuring cGMP compliance for clinical products and representing the Cell Therapy Quality Assurance Department during regulatory inspections. Prior experience includes roles as Quality Assurance Specialist IV and III at Lonza, focusing on compliance with Good Manufacturing Practices and the development of SOPs for both clinical and non-clinical cellular therapeutic manufacturing. Previous positions include Quality Assurance Supervisor at BioReliance, managing a team of auditors, and roles at Covance, Marion DuPont Scott Equine Medical Center, Marsh Thoroughbred Farm, and Veazie Veterinary Clinic, contributing to various aspects of animal care and toxicity testing. Laura LeClair holds a Bachelor's Degree in Animal Science and Pre-Veterinary Medicine from the University of Maine.
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Lonza
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Lonza Group AG (Lonza) is a Switzerland-based holding company and a supplier to the pharmaceutical, healthcare and life-science industries. The Company divides its activities into four divisions: Life Science Ingredients; Microbial Control; Custom Manufacturing, and Bioscience. The Life Science Ingredients division comprises a range of products for applications in nutrition, hygiene, preservation, water treatment, materials protection, and other industrial markets. The Microbial Control division focuses on five areas: hygiene, wood protection, water treatment, oil/gas applications, and industrial preservation and comprises products ranging from disinfectants to household cleaning products. The Custom Manufacturing division comprises products used in pharmaceuticals sector. The Bioscience division comprises bioscience products, including cell culture and molecular biology tools for research, tests for microbial detection, and media used in the production of therapeutics.