QC Technical Writer and Data Reviewer (Lynchburg, VA)
Fleet Laboratories, a Prestige Consumer Healthcare company, prides itself on its ability to adapt to consumers’ needs with creative thinking and innovation in the development of personal healthcare and beauty products that consumers can trust. That trust began over 150 years ago when the CB Fleet Company was founded and continues to this day with our talented and dedicated group of QC chemists who assure that the chemical quality of all raw materials, in-process samples, finished products, and stability samples meet or exceed all quality standards and specifications. Our consumers expect nothing less.
Fleet Labs is growing, and new product development is driving more chemical validation activities, more testing, and more chemical analyses in our cGMP world. That’s why we need a degreed chemist with excellent writing skills to review and write Standard Operating Procedures (SOPs), investigations, protocols & calibration reports, and other various documents. You will manage documentation compliance and change control for the laboratory, review stability database and compendial updates and provide updates to management. You will execute these tasks under current FDA regulations, ICH guidelines, USP methodologies, cGMPs and SOPs and work independently with minimal supervision. In addition, you will provide technical expertise and guidance to our lab staff when performing chemical analyses on raw materials, in-process samples, finished products, and stability samples using established analytical methods, standards, and specifications, plus lead the training and instruction of QC personnel. You will also review and approve Analytical Reports (AR) and use our SAP ERP and Master Control system to enter data. This role also serves as a technical leader and back up to the QC Supervisor.
Requires BS in Chemistry and six years of experience in a quality control laboratory, or an equivalent combination of education and experience that demonstrates proficiency not only in quality systems and lab procedures, but in writing SOPs and other technical documents using Microsoft Word and Excel. Solid knowledge of cGMP regulations is essential.
Come help us improve and develop even more iconic brands that consumers have come to depend upon and trust for over 150 years and apply now.
Prestige is an Equal Opportunity Employer
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