The Lead FW Engineer will primarily execute and lead the Firmware aspects of projects. The role is customer facing and requires the ability communicate technical details to potentially non-technical clients. The role must also translate client needs to a technical team in order to plan, estimate, identify and manage tasks. This role is expected to both develop FW and ensure delivery of technical goals of a team of resources, both internal and externally, on time and within budget.
The Mechanical Engineer will provide technical engineering leadership during the investigation, definition, design, development, and qualification phases of product development.
The purpose of this position is to assume primary responsibility for the ISO 13485 registration and maintenance of the Nectar PD organization. The Medical Quality Engineer is responsible for ensuring the product development service and support activities of medical devices produced meet the requirements of 21 CFR Part 820, ISO 13485, the Medical Device Directive and other applicable regulations and standards. This position supports the operations team (design & engineering) through all phases of our medical products lifecycle. In addition, involvement with the internal audit process is required. This is a part time position.
Our staff has the talent, experience, and expertise required to translate industrial design, mechanical engineering, software and electronics development, and production management services into winning products.