Maximo Consultant
with ERPMESWMS systems and operational excellence initiatives Experience working in regulated industries FDA ISO13485 EU MDR...
with ERPMESWMS systems and operational excellence initiatives Experience working in regulated industries FDA ISO13485 EU MDR...
teams of Supply Chain Quality Managers, Specialists, and Leads located in the EU, North America & Asia continents...
knowledge of the medical device system EU and US with particular focus on Combination products, software and Companion...
updates, and design change documentation Contribute to EU MDR technical documentation and notified body audit readiness...
, and the EU. IntelliPro, a global leader connecting individuals with rewarding employment opportunities, is dedicated...
: NAM, LAM, EU, GCA, EM, APAC adidas Finance / Controlling adidas Global & NAM Procurement External Comms & Touchpoint Specific...
with assigned EU administrator (Dean of Academic Affairs, Academic Advisor, or Program Director) to review student and classroom...
US and international regulatory standards including FDA, EU, ISO, USP, NRC, and cGMP guidelines. Coordinate cross-functionally to align QC...
Canadian an EU import and export trade regulations and their application in day-to-day operational and regulatory decision...
, including FDA 21 CFR Part 820, ISO 13485, IEC 62304 and EU MDR as well as corporate procedures and requirements. What You Can..., including 21 CFR Part 820, ISO 13485, EU MDR, and ISO 14971. Skilled in developing and implementing procedures for various QMS...