. Delta serves customers through its sales offices, R&D centers, and manufacturing facilities at nearly 200 locations... across five continents. Delta has 158 sales offices, 72 R&D centers, and 48 manufacturing facilities worldwide. Throughout its...
on ISO standards, FDA’s QMSR, EU MDR and other regulations as applicable to Mizuho OSI’s products. Familiar with ISO/IEC.../IEEE 12207 (Systems and software engineering — Software life cycle processes) and IEC 62304 (life-cycle requirements...
standards (e.g., IEC 62304). Conduct code reviews, unit testing, and debugging to ensure software reliability and performance... experience with C and C++. Developed and reviewed documentation according to medical device regulatory standards (e.g., IEC...
with standardized testing and R&D projects Maintain test equipment and test facilities and oversee the equipment calibration process... Experience in a fast-paced test environment with flight hardware Able to support R&D efforts in addition to standardized testing...
with standardized testing and R&D projects Maintain test equipment and test facilities and oversee the equipment calibration process... Experience in a fast-paced test environment with flight hardware Able to support R&D efforts in addition to standardized testing...
Job Category: Engineering Job Description: JOB SUMMARY: The R+D Firmware Engineering Testing Manager leads a team... verification and validation activities comply with FDA 21 CFR Part 820, ISO 13485, and IEC 62304. Collaborates with Systems...
in accordance with IEC 62366 and FDA Human Factors guidance. Identify user profiles, tasks, critical use scenarios, usability risks...-Functional Collaboration & Influence: Champion usability, safety, accessibility, and quality across R&D, Engineering, UX...
vendors). Oversee testing (stability/safety/compatibility), regulatory and compliance (including IEC/FDA considerations... architecture, and unit-economics trade-offs. Maintain strong relationships with R&D, QA/Regulatory, and Packaging...
, while effectively partnering with Quality, R&D, Operations, and Regulatory stakeholders to facilitate consensus, resolve disagreements... of IEC 62304 (Medical device software – software life cycle processes). Experience with medical device systems...
vendors). Oversee testing (stability/safety/compatibility), regulatory and compliance (including IEC/FDA considerations... architecture, and unit-economics trade-offs. Maintain strong relationships with R&D, QA/Regulatory, and Packaging...