Vispact is growing in Visp: whoever joins us takes responsibility on real equipment in live GMP operations, in projects for leading life-science manufacturers.
Fig. 01 · Into the cleanroom
Illustrative image
Engineering, validation, quality or digitalisation: from day one you work in live GMP projects at leading life sciences manufacturers. No waiting bench, no practice projects.
We work where decisions are made: at the equipment, in the cleanroom, in the QMS. You know the systems you are responsible for, not just their drawings.
You learn from senior engineers with more than ten years of GMP practice and grow technically: Annex 15, GAMP 5 and ALCOA+ are daily business here, not theory.
Three kinds of know-how you build in our projects: technical, project and regulatory.
Qualification, CSV, data integrity: you work on real systems in GMP operations and build expertise that holds up in an audit.
You take responsibility in live projects of leading life sciences manufacturers: from planning to inspection-ready handover.
Annex 15, GAMP 5, ALCOA+: you learn not just to quote standards but to apply them at the equipment.
You plan and support equipment, processes and utilities across the entire lifecycle, right in the middle of live GMP operations.
You own the qualification lifecycle to EU-GMP Annex 15, from the URS through DQ, IQ, OQ and PQ to requalification, risk-based to ICH Q9.
You validate computerized systems to GAMP 5 and safeguard data integrity to ALCOA+, Annex 11 and 21 CFR Part 11.
You contribute to the QMS, conduct gap analyses and keep documentation audit-proof at all times.
You plan and support PW/WFI, HVAC/cleanroom air and compressed gases so that utility supply remains qualified and ready to operate.
You lead GxP projects across all phases: deadlines, costs, quality and interfaces, from planning to handover.
Convince us with your GxP profile, even if no current opening fits.
Send your CV and three sentences on your GxP experience to info@vispact.swiss. No portal, no cookie-cutter cover letter.
You speak directly with our engineers, technically and at eye level. You quickly sense whether it fits, and so do we.
You receive a clear, honest decision without a holding pattern: short decision paths are part of our process.
Your application does not land in a portal, it lands with me. I read every one personally.
A CV is enough. No templated cover letter.
Neue Stellen und Einblicke aus unseren Projekten finden Sie auch auf LinkedIn.
GxP engineering and validation for life sciences: qualification to Annex 15, CSV to GAMP 5, data integrity to ALCOA+. From Visp in Valais, for Switzerland and Germany.
Vispact GmbH · Mondstrasse 6b · 3930 Visp · Switzerland · UID CHE-160.105.904
info@vispact.swiss