OmniaBio: Associate I, Commissioning Qualification and Validation (Permanent or 12 month Contract)

The Associate I in Commissioning, Qualification, and Validation supports the development and validation of deliverables, standard operating procedures, and systems within a biopharma GMP environment. The role involves assessing documentation for equipment, facilities, and computerized systems to ensure compliance with regulatory standards such as FDA and EU requirements. Collaborating closely with cross-functional teams, this position maintains validation schedules and contributes to risk assessments, SOPs, and deviation management.