Senior Systems Engineer

$50-$60 per hour

Plymouth, MN

Full Time/Contract

Duration: 12 Months Contract

1. Summary

• In the Systems Engineer role, you will be supporting the overall technical direction of Acute Therapies products.

• Based on your technical skills, you will drive various portions of the product development cycle at stages ranging from feasibility through lifecycle management.

• Tasks may include product requirements management, traceability, DHF structure & maintenance, product risk management, system integration, verification, and validation of medical devices.

2. What you'll be doing:

• Perform the activities associated with the systems engineering of one or more products in various stages of the product lifecycle from new product development to post-market surveillance

• Understand clinical and user needs and apply them to product realization

• Capture inputs for requirements from various sources such as user needs, regulatory standards, human factors, quality, manufacturing, service, etc.

• Use knowledge of technology, process, and/or therapy domains to drive solutions and product design realization from a systems perspective

• Craft design concepts and research methodologies that best meet current and future customer / business needs for a product or process domain area

• Create and maintain design history file elements

• Facilitate an improved understanding of the interrelationship between requirements, risk and reliability

• Anticipate technical challenges, risk scenarios, and prepare, lead, and execute mitigation strategies to ensure optimal results

• Resolve systems-related technical issues by applying problem-solving tools such as cause-and-effect diagrams, Pareto charts, etc.

• Propose and drive solutions to technical problems that are ambiguous and diverse in scope

• Perform impact assessments on the requirements on an ongoing basis for any proposed design / material / process changes or observations from field / service / manufacturing. As needed, propose recommended mitigations with rationale.

• Influence stakeholders and cross-functional team members within the project

• Drive adherence to FDA, ISO and IEC design control procedures, regulations and standards

• Use various software tools and programs to complete the above responsibilities

3. What you'll bring:

• Sound knowledge of systems engineering and related areas such as electro-mechanical and software engineering

• A track record in electro-mechanical system development, preferably in medical devices or other regulated products such as aerospace, automobile, or military

• Knowledge of DOORS, Teamcenter, TrackWise8, JIRA, and ALM preferred

• Familiar with statistical methods/tools for design and verification, e.g. DOE, sample size

4. Experience and/or Background:

• Bachelor's or master's degree in electrical, Software, Mechanical, Biomedical, or a related engineering or science discipline

• Three or more years of relevant experience

About US Tech Solutions:

US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To learn more about US Tech Solutions, please visit

US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

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