Senior Validation Specialist I -WYETH-USA- Pearl River, NY

in

With proven ability to accomplish projects independently, provides validation engineering of cGMP equipment systems and processes. Based on engineering specifications, performs validation projects that includes authoring protocols, executing validation protocols and writing reports of validation results. Leads the validation activities for large capital projects. Ensures timely resolution of all deviations and changes that occur during the execution phase. Assists in developing validation standards, procedures, and guidelines for the utilization within the Validation department. Will represent the Validation department on cross-functional site teams. Provides guidance to more junior members of the Validation Engineering staff.

Job Responsibilities

*Leads projects by developing Validation master plans, schedules, resource loading, and other project deliverables as required. Based on engineering specifications, validates large capital and technically complex projects on equipment or processes that includes authoring protocols, executing validation protocols, and writing reports of validation results.

Click Here For More Information