Senior QA Specialist - Deviation & CAPA Lead (Contract)

A leading pharmaceutical company is seeking a Senior Quality Assurance Specialist in Colorado. The ideal candidate will own end-to-end deviation investigations, ensuring compliance and accuracy in quality event documentation. With at least 8 years of experience in deviation investigation, the specialist will provide clear, concise reports in a GMP setting. Strong project management and communication skills are essential. This contract role offers an opportunity to work within a dynamic team focusing on quality assurance and continuous improvement. #J-18808-Ljbffr