Kintiga supports pharma, biotech and other health‑technology developers across the value chain to bring innovative solutions to patients. They are looking for a Regulatory Affairs professional with a strong scientific background (Master’s/PhD) and solid experience within the pharmaceutical industry or consulting environment.

You’ll bring proven knowledge of local and EMA regulatory requirements, with added value if you’ve previously supported RIP activities or worked with EU/Local GVP.

Read the full job description here.