Staff Device Engineer
product complaints, regular review of DHF, and post-market surveillance as related to on-market products. This role interacts...
product complaints, regular review of DHF, and post-market surveillance as related to on-market products. This role interacts...
standards. Hands-on experience with design control, risk management, and technical documentation (DHF, traceability matrix...
: MDR & Regulatory Execution Own and produce MDR-required artifacts, including Design History Files (DHF), Technical...
: MDR & Regulatory Execution Own and produce MDR-required artifacts, including Design History Files (DHF), Technical...
Execution Own and produce MDR-required artifacts, including Design History Files (DHF), Technical Files, Software...
: MDR & Regulatory Execution Own and produce MDR-required artifacts, including Design History Files (DHF), Technical...
manufacturing, conducting product verification/validation, and developing DHF documentation and test protocols compliant with FDA...
: MDR & Regulatory Execution Own and produce MDR-required artifacts, including Design History Files (DHF), Technical...
' sleep and respiratory medical devices. Core Competencies Quality Management System (QMS) Design Controls (DHF, DMR... goals and objectives. Own the Design Control process (21 CFR 820.30), ensuring proper documentation of DHF, DMR, and DHR...
, ensuring alignment with design control and DHF requirements. Basic Qualifications: Bachelor’s degree in Packaging...