Computer system validation and lifecycle services for biopharmaceutical manufacturing
Valspec operates a validation and systems engineering practice focused on manufacturing automation and IT infrastructure in life sciences. The stack—anchored in Emerson DeltaV, Rockwell Automation, and Siemens controls, plus enterprise virtualization (VMware, vSphere, Citrix)—reflects deep domain specialization in regulated manufacturing environments. Hiring momentum is decelerating (3 roles in 30 days across an 18-person open pipeline), with senior engineers representing the largest cohort, signaling either selective growth or stabilized team structure.
Valspec provides computer system validation (CQV), commissioning, qualification, and lifecycle services to pharmaceutical and biopharmaceutical manufacturers. The company specializes in qualifying manufacturing automation systems, IT infrastructure, laboratory information systems (LIMS via Labware), and manufacturing execution systems (MES), with explicit focus on FDA and cGMP compliance. Active projects span automation controls integration, risk management in large-scale facilities, validation documentation, and disaster recovery implementations. The business operates from Royersford, Pennsylvania, with 51–200 employees and currently hires exclusively in the United States.
Control systems: Emerson DeltaV, Allen-Bradley, Rockwell Automation, Siemens, Honeywell, OSI PI. Enterprise: VMware vSphere/ESXi, Citrix, Veeam backup, HPE infrastructure, Windows Server, Active Directory. LIMS: Labware.
Current projects include CQV of manufacturing equipment, MES validation, automation controls integration, risk management in biopharmaceutical facilities, validation documentation, backup/disaster recovery solutions, and FDA/cGMP compliance support.
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