Validation Specialist I

The Validation Specialist I is responsible for supporting the execution of validation activities for laboratory equipment within a regulated pharmaceutical manufacturing environment.

This position will support the qualification and validation of various laboratory instruments and equipment, ensuring compliance with applicable cGMP requirements, company procedures, validation protocols, and regulatory standards.

The role requires hands-on participation in validation execution, documentation, discrepancy resolution, and collaboration with Quality, Laboratory, Engineering, and other cross-functional teams.