GxP consulting and validation services for pharma and life sciences manufacturers
Verista operates a full-service consulting practice supporting life-sciences manufacturers through compliance, validation, and quality challenges across product development and manufacturing. The tech stack reflects a manufacturing-first operation: core systems (SAP, ServiceNow, LabVantage) sit alongside specialized pharma-grade tools (Veeva QualityDocs, DeltaV, Maximo, Oracle Primavera), with active projects centered on equipment qualification, process validation, and site-wide modernizations. Engineering dominance in hiring (30 of 48 open roles, weighted toward senior/principal levels) signals scaling of complex validation and automation work.
Notable leadership hires: Quality Lead
Verista is a business and technology consulting firm serving life-sciences companies across the preclinical, clinical, commercialization, manufacturing, and distribution stages. The firm employs 650+ experts across four U.S. locations (Indiana, Pennsylvania, Massachusetts, California) and specializes in computer system validation, quality management systems, manufacturing automation, and regulatory compliance (21 CFR Part 11, cGMP, GDP). Current projects focus on equipment qualification, process validation, manufacturing scale-up for granulation and spray drying, and SAP integration for serialization — addressing internal pain points around GMP compliance, process robustness, and manufacturing efficiency. The client base includes traditional manufacturers and contract manufacturers transitioning to CDMO models.
Core ERP/operations: SAP, ServiceNow, Microsoft Office suite. Pharma-specialized: LabVantage (LIMS), Veeva QualityDocs (QMS), DeltaV/Emerson (process control), Maximo (maintenance), Oracle Primavera (project management), SharePoint (collaboration).
Fishers, Indiana. Additional offices in Wayne, Pennsylvania; Westford, Massachusetts; and San Mateo, California.
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