
CURIA is a CDMO partnering with customers to make treatments accessible through its biologics and small molecule expertise.
Quality Control Analyst I, II, or III performs complex testing and data evaluation, troubleshoots issues, and maintains accurate records. The role involves working with regulatory and compliance guidelines, interacting with other departments, and leading projects. The ideal candidate has a Bachelor's degree in Chemistry or a related field and relevant experience in cGMP or GLP pharmaceutical industry environments.