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Job DescriptionHeadquartered in Nashville, TN – one of the fastest-growing and most exciting cities in the United States – August Bioservices is a privately-owned, high-growth, and high-impact Contract Development Manufacturing Organization (CDMO). As a US-based outsourcing partner that provides a wide array of expert drug discovery, drug formulation, and drug manufacturing services to pharma and biotech companies of all sizes, we play a vital role in the global pharmaceutical industry. Our work is instrumental in helping to develop molecules today that can become the life-changing therapies of tomorrow. To support our growth plans, August is investing significant capital in a two-phase expansion project – including building a new state-of-the-art facility adjacent to our current facility. For those seeking dynamic opportunities, rewarding career paths and a chance to make a difference in global health, come grow with August! August Bioservices is looking for an Analytical Development team member that is passionate and driven regarding his/her work. August Bio desires a team member eager to work in an environment where people are motivated to do their best for the company and its clients. The Analytical Chemist I & II position, reporting to the Analytical Chemistry Supervisor, will operate under minimal supervision to perform chemical analyses of samples according to standardized procedures to determine the identity, content, purity, stability, and other characteristics of the samples analyzed. He/she may perform method development activities related to the development of methods for testing of raw materials and clinical drug product as well as formulation development.Responsibilities • Performs routine laboratory testing and duties, • Performs laboratory investigations in support of testing, • Troubleshoots analytical equipment, • Accurately documents all necessary and relevant information in a clear and concise manner per cGMP requirements, • Responsible in the development of analytical chemistry procedures to determine the identity, purity, stability, and other characteristics of samples that are analyzed, • Author and execute method validation protocols, • Author method validation reportsRequirements, • Bachelor’s Degree in chemistry, biology, or related science, • 2+ years of pharmaceutical experience or equivalent., • Self-starter and ability to work independently, • Strong written/verbal communication and presentation skills, • Able to work flexible schedules on a short notice