Description
The role provides technical support and documentation services for FDA-regulated life sciences clients, including preparing and maintaining SOPs, work instructions, forms, and technical reports; ensuring compliance with cGMP and regulatory requirements; supporting training and coaching; maintaining client relationships; and identifying project opportunities. It requires a bachelor’s degree in engineering, science, or a related technical field, knowledge of cGMP and FDA regulations, strong documentation and analytical skills, and the ability to work under supervision and in multidisciplinary teams.
