Regulatory Product Manager - Medical Software (MDR)

pQUMEA is seeking a regulatory-enabled professional to translate MDR and standards into product and engineering requirements. You will own requirements engineering, traceability and verification activities across software, algorithms and devices, while shaping VV evidence and documentation. /ppJoin a Swiss MedTech team driving regulatory excellence for innovative radar-based patient monitoring solutions, collaborating closely with software, AI, and clinical partners. /p #J-18808-Ljbffr