Compliance and digital transformation for regulated manufacturing
Plantvision AB builds digital solutions for manufacturers operating under strict regulatory frameworks—pharma, biotech, medical devices. Their tech stack (ISO 13485, ISO 27001, .NET, Siemens automation tools) and pain-point focus on GxP compliance, equipment validation, and computerized-system qualification reveal a company solving for risk-averse, audit-heavy environments where process control and traceability are non-negotiable. Senior-heavy hiring (6 of 10 open roles) paired with active projects on lab relocation and IT system implementation signal work on large transformation engagements.
Plantvision AB operates in digital transformation and quality assurance for highly regulated manufacturing sectors—pharmaceuticals, medical devices, and life sciences. Founded in 1999 and based in Kista, Sweden, the company specializes in process digitalization, compliance architecture (ISO 13485, ISO 27001), and equipment qualification. They work across lab operations, production lines, and quality systems, with a particular focus on validating computerized systems and managing GxP-regulated environments. Their services span technology consulting, change management, and academy/training delivery. The team is concentrated in Sweden and currently operating at minimal hiring velocity.
Pharma, biotech, medical devices, and life sciences—sectors requiring ISO 13485 and GxP compliance. Work includes lab relocation, equipment validation, and process digitalization.
ISO 13485, ISO 27001, .NET, VBScript, Siemens TIA Portal, WinCC, and Ignition. No major tech migrations or new adoptions currently noted.
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