As a quality engineer for medical devices, you oversee the continual improvement of medical devices as well as the design and manufacturing of new devices. Your duties are to develop prototypes, assess the quality of manufacturing standards, and develop guidelines for technological improvement. You also work closely with medical device engineers to ensure sufficient documentation and standardization, which helps users and service technicians test and maintain the safety of devices. Your responsibilities as a medical device quality engineer relate to all aspects of the product life cycle, from prototyping to the supply chain to production.
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Industry leading AI capabilities meet business focused solutions
We are a global corporation with dedicated Healthcare and Engineering professionals on our workforce. Our expertise lies in the fields of Medical, Pharmaceutical, and Automobile industries. With an extensive network spanning across the USA, we collaborate with Medical device and Pharmaceutical companies nationwide.
Our direct engagement with client managers, Prime Vendors, and Suppliers involves continuous updates on our latest resources’ skill sets, potential projects, and noteworthy FDA/Regulatory intelligence news.
Supported by an exceptionally robust Legal team, we possess a wealth of experience in navigating complex scenarios. Our well-structured team, all based in the USA, includes specialized units for Marketing, Legal, HR, and Leadership.
Ensuring round-the-clock support, we leverage offshore employees, facilitating 24/7 availability. Our highly compensated and seasoned resources attract 8-10 project requests daily from both clients and vendors, underscoring our reputation for excellence.
