Pharma compliance and validation services across facilities, processes, and equipment
PharmEng Technology is a Toronto-based compliance engineering firm now operating within Efor Group's global network of 3,000 experts. The tech stack—heavy on legacy pharma tools (SAP, LIMS, OSIsoft PI, Veeva Vault, Documentum) paired with engineering platforms (Primavera P6, Teamcenter, Desigo CC)—reflects a business rooted in capital-project execution and equipment qualification. Recent adoption of DeltaV and SCADA signals expansion into real-time process control and automation, while the engineering-dominant hiring profile (33 of 86 active roles) confirms core focus on hands-on commissioning and validation work.
PharmEng Technology delivers technical services in commissioning, qualification, and validation (CQV) for pharmaceutical, biotech, and medical-device manufacturers. With over 25 years of industry experience, the firm serves mid-to-large clients on facility upgrades, process validation, equipment qualification, and regulatory compliance—including GDP, GMP, and quality-management-system implementation. Operating from Toronto and now supported by Efor Group's footprint across 12 countries, PharmEng combines global engineering resources with local project delivery. Current workload spans facility and process upgrades, product-recall management, technical-transfer activities, and audit-readiness programs.
PharmEng is recruiting across 25 countries including Canada, USA, Spain, Brazil, Mexico, multiple EU nations (Denmark, Poland, Sweden, etc.), and Asia-Pacific (China, Singapore, Indonesia).
Core platforms include SAP (ERP), LIMS and MES (lab/manufacturing execution), Veeva Vault and Documentum (document management), Primavera P6 and Oracle Unifier (project controls), and pharma-specific tools like OSIsoft PI, HPLC, and Seeq for process monitoring.
Yes—actively adopting DeltaV and SCADA systems, indicating expansion into real-time process control and automation for pharmaceutical facilities.
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