Descriptions: Design| Configurations Development using Opcenter EX Core MDD Semi Electronics Hands on experience on Designer| Portal...
, or pharmaceutical industry. Strong execution knowledge of QMS systems, FDA regulations, ISO 13485, MDD / IVDD / IVDR / MDR/ ISO14971...
, FDA (Food & Drug Administration) & MDD (Medical Devices Directive) based quality systems. Responsible for ensuring...
requirements (GMP, ISO, MDD), EES policy and procedure requirements. Qualifications / Requirements: A bachelor’s degree...
of medical device management. Well versed in US FDA and EU MDD/MDR requirements A thorough knowledge of related disciplines...
Inspector in accordance with MDD-00948/MDD-01464. Qualifications: Required: High school diploma or GED. 1+ years...
to meet governmental regulations such as FDA QSR, ISO 13485, the MDD, and knowledge of relevant standards. Ability to detail... (e.g. traceability, QSRs, ISO, MDD/MDR requirements) and other applicable regulations. Experience working with ERP/MRP...
including ISO 13485, MDD, and FDA. Develops methods, standards, procedures, plans, processes, programs, and schedules to meet...
with MDD-03128, MDD-01505, MDD-02268, MDD-01737, EBP-03287 Proficiency with Microsoft Office Suite (including but not limited...
within a Medical device or other regulated industry with knowledge of Risk Management (ISO 14971 2019), MDD (Medical Device Directive...