Description
The Validation Technician II executes installation, operational qualification, and requalification protocols for equipment and utilities used in sterile pharmaceutical drug analysis and manufacture. The role includes protocol execution and reporting, data analysis, troubleshooting, change-control support, requalification coordination, and documentation in compliance with FDA guidance, cGMP, and health and safety requirements. The position reports to the Validation Supervisor and requires a high school diploma or GED equivalent with two years of relevant experience, or an associate’s degree with one year of relevant experience, along with strong technical writing, communication, planning, and organization skills.
