In this role, you will be responsible with limited oversight for the mechanical testing aspects of a project, participating on cross-functional project team through all phases of the product development process, and assisting the technical team with planning executing, documenting and communicating testing activities.
This position is responsible for planning and executing the integration of Internet based products and services for ESPN into a complex data center and cloud environment in an efficient, secure, scalable, reliable and cost effective manner. This includes any content delivery systems, hardware configuration, custom software implementation, cloud systems design, performance and process improvement, and systems documentation.
The Staff Electrical Engineer performs broad based electrical design, development, review, and documentation. Success in this role is predicated on an individuals ability to contribute technically under FDA regulated medical device design process while actively contributing to work efforts and reporting project status to project management.
In this role, you will develop and/or execute software testing and validation procedures, programming and documentation; work autonomously in an area of specialization to analyze user needs and develop software solutions working on problems of diverse scope.
In this role, you will track all LIPA protection related compliance for the bulk power system and Bulk Electric System assets and the under frequency Load Shed relay systems and digital fault recorders.
In this role, you will monitor, review, evaluate, make recommendations to optimize the performance of the protection systems and test programs associated with the LIPA T&D system and the associated regulatory compliance requirements.
In this role, you will handle multiple projects and tasks utilizing a high level of written and oral communication skills. The selected candidate will be responsible for providing quality leadership, guidance and support in design control methodologies for electromechanical/software medical device designs.
In this role, you will be responsible to develop and make updates to applicable site / unit procedures and policies. Coordinate quality systems and processes to ensure compliance with quality system and regulatory requirements and promote quality improvements.