Senior Validation Specialist I -WYETH-USA- Pearl River, NY
Accomplish validation tasks on small to medium projects independently, provides validation of cGMP Laboratory Instruments. Based on manufacturers and laboratory specifications, performs validation projects that includes authoring protocols, executing validation protocols and writing reports of validation results. Represent the Validation department to contribute to Validation Master Planning on specific projects. Ensures timely resolution of all deviations and changes that occur during the execution phase. Develop validation standards, procedures, and guidelines for the utilization within the Validation department with guidance from supervisor. Leads the validation activities for medium scale projects. Will represent the Validation department on cross-functional site teams