This position is responsible for supporting analytical method transfer and validation activities to ensure robust and compliant testing of biologic products.Collaborate with internal and external partners to execute method qualification, validation protocols, and transfer documentationData analysis, protocol/report generation, and troubleshooting analytical techniques such as HPLC, CE, and ELISAThe role requires strong technical expertise and attention to regulatory requirements in a GMP-compliant environmentThis role is onsite in Sanford, NC. There are no public transportation options to the site. Ability to support outside standard hours may be needed.
