Validation Engineer II

Location : Portsmouth NH Validation Engineer II responsible for Computer System Validation (CSV) in a regulated biotech/pharma manufacturing environment, ensuring GMP compliance for automation, process control, and MES systems while supporting site and process improvement initiatives. Job Responsibilities: Own CSV activities for equipment, automation, and computer systems Perform risk assessments, review change requests, and validate test scripts Draft and execute validation protocols and manage GMP documentation updates Lead Change Control, Deviations, and CAPAs within the QMS Support and validate DCS (DeltaV) and MES (Syncade) systems Collaborate with cross-functional teams to improve validation efficiency and compliance Skills: Computer System Validation (CSV) in GMP environments Process Control Systems & Automation DeltaV DCS (preferred) and MES (Syncade) Biotech/Pharma or biologics manufacturing experience QMS processes (Change Control, Deviations, CAPA) Education/Experience: Bachelor's.