Description
We are seeking a Sr. Electrical Engineer to join our team in St. Paul, MN. 

Education

• Bachelor’s Degree in Electrical Engineering or a related engineering field (required).
• Advanced credential or professional certification in a relevant discipline/concentration (desired).

Experience

• 7+ years’ experience required.
• Training and experience in manufacturing processes and methods desired, especially in the manufacturing of medical devices.
• Experience working in a broader enterprise/cross-division business unit model preferred.
• Six-Sigma knowledge and experience desired.

Skills & Qualifications

• Relevant work experience in performing the layout, construction, and evaluation of a variety of prototype Printed Circuit Boards, fixtures, and tools.
• Demonstrated ability to develop new design features as part of existing systems.
• Documented record of delivering tool engineering information that adds value to management’s decision-making process.
• Strong knowledge of and compliance with FDA regulations and Company operating procedures, processes, policies, and tasks.
• Advanced personal computer skills: spreadsheet, word processing, database management, and specialized applications.
• Ability to work in a highly matrixed and geographically diverse environment.
• Ability to work both independently and in a team within a fast-paced, changing environment.
• Strong verbal and written communication skills with the ability to communicate at multiple organizational levels.
• Strong organizational and follow-up skills with attention to detail.
• Ability to multitask, prioritize, and meet deadlines in a timely manner.
• Ability to leverage and/or engage others to accomplish projects.

Duties & Responsibilities

• Lay out and construct a variety of prototype tools and fixtures required for development purposes.
• Conduct evaluations, tests, and analyses related to feasibility and function.
• Perform troubleshooting and fault isolation on a variety of breadboards and hybrids.
• Conduct measurements specified in design verification plans, document and tabulate results, and provide engineering test reports.
• Document custom tools with specifications, schematics, and mechanical layouts to support document control and tool release.
• Comply with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments.

Maintain positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.