Latest Medical Risk Management jobs in Orange County

7 Medical Risk Management Jobs in Orange County

Senior Regulatory Affairs Program Lead – Medical Devices ClinChoice - Irvine, CA, United States Medical Device Regulation (MDR) 2017/745 F. Proper application of Quality Management System Standard ISO 13485 G. Proper application of Risk Management Standard ISO 14971 H. Familiarity with International 2 days ago
Staff Engineer, Product Risk Management Johnson and Johnson - Irvine, CA or another highly regulated industry. * At least two (2) years of experience performing Medical Device Risk Management. * Critical thinking and investigation skills. * Ability to multitask, including ability 5 days ago
Director, Medical Device & Combination Product NPI Quality AbbVie - Irvine, California business processes supporting new product introduction including risk management. Builds and maintains relationships with R&D, R&D QA, Regulatory Affairs, E&PQA, S&T, ECM, PSM, and Global Supply Chain 6 days ago
Quality Engineer Katalyst Healthcares & Life Sciences - Irvine, California , and procedures. Requirements: Knowledge of Medical procedure and corresponding Medical Equipment Knowledge of Medical Equipment manufacturing processes Knowledge on Quality Management and its tools & techniques 15 days ago
Forum: Start a Discussion Join
Medical Device Safety Engineer (IEC 60601-1) Lake Forest,California Stellent IT LLC - Lake Forest, CA and maintenance of commonly used safety equipment, and calibration procedures. Working knowledge of ISO 14971 Risk Management for Medical Devices in medical device products safety compliance, and/or fully 22 days ago
Quality Engineer (Complaints) Katalyst Healthcares & Life Sciences - Irvine, California . Responsibilities: This consultant will come from a Medical Device background and will be responsible for remediating existing complaints. This role is focused heavily on root cause analysis, risk management, data 22 days ago
Senior Regulatory Affairs Program Lead Johnson & Johnson - Irvine, CA of the European MDD, MDR and CE marking is preferred. Familiarity with Risk Management Standard ISO 14971 is preferred. Direct experience with international medical device registration is preferred. Experience USD 104,000.00 - 140,000.00 per year 29 days ago

Top locations