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The Senior CQV Engineer at CAI is responsible for developing documentation related to commissioning, qualification, and validation of pharmaceutical facilities. This role includes protocol writing and execution, field verification, and overseeing small teams for project coordination at client sites. The Engineer will ensure compliance with FDA regulations and provide leadership in cGMP practices while actively participating in troubleshooting and problem-solving.

The Project Manager will lead cGMP initiatives, managing mid-sized to large projects in the Life Sciences sector, focusing on commissioning and validation activities. Responsibilities include oversight of CQV services, document management, progress tracking, and resource allocation to ensure project deliverables are met efficiently.

The Program Manager leads the Digital Enablement program, acting as a liaison between Professional Services and development teams. Responsibilities include managing communication strategies, overseeing project lifecycles, advocating for digital initiatives, and establishing performance metrics for program success.