We help Life Science companies reduce their manual test execution and documentation effort by 40–60%
"We don't automate validation decisions. We automate everything around them."
We help life science companies automate test execution and evidence packaging for GxP systems, so validation experts can focus on decisions, not documentation.
Orchestrated test execution with environment prep, data setup, and run sequencing. Test execution is handled consistently every time without manual coordination.
System-generated, timestamped evidence that's indexed and audit-ready. No more screenshot stitching or missing documentation.
Experts review exceptions and approve outcomes. Validation decisions stay with the right people.
Validation packages generated automatically with complete traceability, fewer review loops, and faster release readiness.
We work with regulated teams who run validation and struggle with manual test execution and documentation.
Pharma teams across manufacturing, quality, lab, clinical, and enterprise GxP and non-GxP systems with frequent change and high-volume, evidence-heavy regression testing.
Contract manufacturers managing multiple client systems with tight validation timelines.
Device companies with quality systems requiring continuous validation and evidence management.
Release timelines are being pushed by manual test execution, heavy QA review cycles, and time-consuming evidence packaging.
"Change keeps scaling, but validation throughput cannot scale manually."
We combine regulated delivery expertise with trusted automation engineering and platforms to accelerate testing and evidence generation.
Global automation and digital transformation leader delivering AI-powered intelligent automation and test automation as a service.
7-time Gartner Magic Quadrant Leader in RPA—the industry-leading platform for building software robots that automate repetitive tasks, integrate systems, and scale enterprise workflows.
Experience and expertise you can trust
Jón Pétur founded PMC - Pharma Management Consulting in 2023 to provide specialized Scrum Master, IT Project Management, and Compliance Services to the life science industry. With over 11 years of IT consulting experience and 8 years focused exclusively on pharmaceutical GxP systems, he brings deep expertise in validation automation, digital transformation, and agile methodologies.
As a trusted consultant, he has delivered critical GxP projects for leading pharmaceutical and medical device companies including Novo Nordisk, NNIT, Novartis, Orphazyme, Oncopeptides, Ascendis Pharma, Zealand Pharma, Santen Pharmaceutical, Elos Medtech, Epista Life Science, and Emerson Process Management. His versatile expertise spans roles as SCRUM Master, Technical Project Manager, System Manager, Compliance Consultant, and Validation Lead, adapting to each client's unique needs and regulatory requirements.
In 2026, Jón Pétur partnered with Valenta to bring specialized validation automation solutions to the pharmaceutical industry. Together, we combine deep pharma expertise with proven automation technology—enabling clients to scale validation throughput without scaling headcount.
Key project experience includes MES/OT gateway integration with eSCADA using Ignition, SIEMENS UMC implementation, Veeva and TraceLink serialization design and validation, QMS and laboratory system implementations, and optimization of IT validation processes using Risk-Based Validation (RBV) approaches. He has also managed infrastructure relocations from on-premises to cloud environments.
Education: M.Sc. Engineering Management from Technical University of Denmark, with exchange studies at National University of Singapore. B.Sc. Engineering Management from University of Reykjavik.
Certifications: Certified SAFe® 6 Scrum Master, TraceLink Implementation Project Manager, TraceLink Administrator, LEAN Six Sigma Green Belt.
Based in Copenhagen, Denmark, we focus on serving clients in the Copenhagen area and throughout the Nordics.
Let's explore how we can remove the validation bottleneck in your operations.
Chat with us about validation automation