About Us
Regulation, process and system are one task here, not three separate responsibilities.
Our focus covers four fields: pharmaceuticals, medicine, biotechnology, and the supplier industries that have to meet GxP requirements.
Learn moreWhy Significon
We start with the business process. From there we derive what the systems must deliver, what validation has to cover and what operations needs.
Shorter cycle times, less capital tied up, faster batch release: that's what we design your GxP processes for — along the material flow and in the processes that support it. Compliance is the prerequisite, efficiency the difference.
Learn more →Know the processes, know the risks, focus there: that's the risk-based approach FDA and GAMP promote today. We derive risk top-down from business processes, not from system functionality. The result: validation depth where it matters, and a proportionate effort everywhere else.
Learn more →We think beyond the individual system. We design business processes end to end, including where other systems and departments take over. The result: systems that fit the process, instead of processes that bend to the system.
Learn more → About Us
Our focus covers four fields: pharmaceuticals, medicine, biotechnology, and the supplier industries that have to meet GxP requirements.
Learn moreWho we are
Significon is a team from Mainz that knows regulated processes from operations, not just from the rulebook.
22
Specialists
100%
Life sciences focus
5
Academic disciplines in the team
DE/EU
Project deployments
Pharmacy · Chemistry · Biology · Engineering · Business
Careers
100% permanent contracts. Flat hierarchies. European team retreats.
Apply now