Engineering consultancy for pharma, industrial, and commercial project delivery
Tandem is a 51–200-person engineering consultancy operating across Ireland, UK, Benelux, and USA, focused on project management, multi-disciplined design, construction, and health & safety for pharma and industrial clients. The tech stack is heavily rooted in legacy industrial automation (Rockwell PlantPAx, Siemens S7, GE iFIX) and design tools (Revit, AutoCAD, Naviswork, BIM), with Microsoft Office and Teams as operational backbone — a profile consistent with on-site, complex, regulated-environment delivery. Active hiring is accelerating (11 new roles posted in the last 30 days) with a senior-weighted mix (11 senior vs. 6 mid-level), suggesting they're scaling delivery capacity for multi-disciplinary pharma and industrial projects.
Tandem delivers end-to-end project execution across pharmaceuticals, industrial, and commercial sectors. Their service lines span project management from concept through completion, multi-disciplined engineering design, construction management, health & safety advisory, and contract staffing. The company operates as Project Managers, Engineering Designers, Construction Managers, PSDP/PSCS roles, Safety Auditors, and Health & Safety Coordinators. Active projects cluster around pharmaceutical site expansion, equipment qualification and validation, GMP compliance activities, new product introductions, and process development studies. Core pain points center on GMP compliance, managing multi-disciplinary teams, documentation standards, audit readiness, and minimizing production disruption during site work.
Core stack includes Microsoft Office suite (Word, Excel, PowerPoint, Teams, Project, SharePoint, Access), industrial automation platforms (Rockwell PlantPAx, Siemens S7, GE iFIX, MES, DCS), and design tools (Revit, Navisworks, AutoCAD, BIM). TIA Portal for Siemens configuration is also in use.
Active projects focus on pharmaceutical and industrial sectors: new product introductions, GXP system validation documentation, pharmaceutical site expansion and fit-out, equipment qualification and validation, building upgrades, access control systems, and continuous CQV improvement initiatives.
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