The Systems Engineer will be responsible for overall system design, development and support; the Systems Engineer installs, tests, maintains, documents, and provides technical support for systems software, as well as modifying existing and creating new systems software for specific enterprise needs.
This position is responsible for providing professional quality engineering service and technical support involving technical quality, in-process quality, and customer service. Supports total quality program to improve cost, productivity, yields and customer requirements.
Support manufacturing to ensure Bill of Materials accuracy and modifications based on Continuous Improvement activities; procure and allocate resources on identified capital investments projects related to equipment, process, and facilities.
This position is responsible for maintaining machine, robot, or measuring program, equipment prints and documentation. Duties and tasks are standardized. Resolves routine questions and problems, and refers
more complex issues to higher levels.
Responsibilities include but not limited to direct engineering support of production and continuous improvement
activities. Duties and tasks are standardized. Resolves routine questions and problems, and refers more complex issues to higher levels.
Process improvement and production support to Manufacturing Facilities through the company; responsible for improving manufacturing reliability, building employee capability, and creating operational stability.
Works closely with the Quality department to ensure implemented improvements are in compliance with ISO standards and overall Quality Management System and monitors the new processes to ensure they work as intended.
Performs full range of standard work for the professional field. Refers complex, unusual problems to others. Identifies and resolves more complex problems and applies problem-solving skills in order to deal with most situations.
Quality Engineer will provide Quality and Compliance related support to the manufacture and distribution of medical devices in accordance with applicable medical standards and regulations (ISO 13485, 21 CFR 820, etc.).