Senior Validation & Quality Engineer - MedTech CDMO

pVivolta in the Netherlands is seeking a hands-on Quality Engineer to strengthen the Quality team in a regulated CDMO environment. You will lead validation activities, develop test methods, and support SPC and process validation in collaboration with Manufacturing, Engineering and RD. /ppThe role emphasizes ISO 13485:2016, FDA and EU MDR compliance, QMS maintenance, internal and external audits, CAPA, risk management, and documentation discipline. /p #J-18808-Ljbffr