The Validation Associate supports qualification and validation activities for facilities, utilities, equipment, and manufacturing processes within a cGMP-regulated oral solid dosage pharmaceutical environment. This role is responsible for authoring, executing, coordinating, and maintaining validation documentation and related quality system records to ensure systems and processes remain compliant, effective, and inspection-ready. The Validation Engineer partners closely with Manufacturing, Packaging, Quality Assurance, and other cross-functional teams to support validation lifecycle activities, change implementation, and continued operational compliance. This position supports manufacturing, equipment, process, and cleaning validation activities within an oral solid dosage pharmaceutical environment and is not a computer systems validation (CSV) role.

Key Responsibilities:

• Author, execute, and mainta...