Pharma Quality Investigations Writer - Deviation & CAPA Lead

A pharmaceutical development company is seeking a Technical Investigation Writer at their Greenville, NC site. This role is responsible for authoring and managing quality event investigations, ensuring compliance and high-quality documentation. Ideal candidates will have a Master's degree in a science-related field or equivalent experience and skills in technical writing, problem-solving, and root cause analysis. Join a fast-paced team dedicated to bringing life-saving products to patients. #J-18808-Ljbffr