Science, applied
We're a CDMO, not a journal — but the science is real and the standards are exacting. Your ideas turn into validated processes that make medicine.
At Diabryx, your work ships in real programs for real patients. We're a team of scientists, engineers, and operators who move fast, hold a high quality bar, and genuinely enjoy solving hard problems together.
We're a CDMO, not a journal — but the science is real and the standards are exacting. Your ideas turn into validated processes that make medicine.
Lean, cross-functional teams own programs end to end. You'll see your decisions land — and you'll have the autonomy to make them.
We're proud of clean inspections and reproducible batches. Doing it right beats doing it fast — and we manage to do both.
Design and optimize IVT and purification processes, and lead transfer into GMP. PhD plus 4+ years in RNA or biologics process development.
Operate and advance the FluxMix™ microfluidic platform, run encapsulation studies, and support scale-up. Background in microfluidics or formulation engineering.
Develop and qualify modality-specific methods for identity, integrity, capping, and encapsulation. Hands-on chromatography and particle analysis experience required.
Own batch disposition, deviations, and audit readiness across our drug substance and drug product suites. 6+ years in GMP QA, with inspection experience.
We're always glad to meet talented people. Send us your CV and tell us what you'd love to work on.