You will keep the system compliant with ISO 13485, FDA QMSR, 21 CFR Part 11, MDSAP, and EU MDR, and you will look for practical ways to make core processes like document control, CAPA, nonconformance, and supplier management work better for the people who use them. Run and continuously improve core QMS processes and workflows, including document and change control, training, CAPA, nonconformance, internal audits, risk management, and production and process controls.