Senior QC Specialist — Method Dev & Release

A leading pharmaceutical company in Dartmouth, MA is seeking a Senior Specialist in Quality Control to oversee contract organization method development and product release processes. The role requires strong knowledge of regulatory testing and method validation in both large and small molecule industries, along with at least 6 years of experience in cGMP environments. This position offers comprehensive benefits, including medical insurance, a retirement plan, and generous paid time off. #J-18808-Ljbffr