Biomedical Engineer

Biomedical Engineer Job Summary

Assist in designing and evaluating biomedical devices and systems,supporting innovation and quality in healthcare technologies.

Contribute to project development with an emphasis on reliability,safety and compliance. Learn and apply foundational engineering principles to deliver effective solutions for the biomedical field.

May perform clinical and preclinical assessments. Typically requires a bachelor's degree in engineering, mathematics, orrelated scientific field. Requires basic skill set and proficiency.

Conducts work assignments as directed. Closely supervised with little latitude for independent judgment.

• Development of unmet needs / voice of the customer requirements/ design inputs
• Ideation and concept development
• Development of designs / specifications / test methods /processes / manufacturing methods
• Test protocol development, benchtop / in vitro / in vivotesting, and report writing
• Employing analytic methods to evaluate concepts and designs
• Ensuring thorough and compliant design documentation
• Conducting risk analyses per applicable standards
• Conducting biomedical product / process / system / prior artbenchmarking
• Developing cost of goods or cost of service models
• Participating in design review meetings
• Support regulatory approval processes and submissions
• Working with cross functional project teams, including physicians, researchers, manufacturers, and other related expertsor project partners
• Contributing to new intellectual property via lab notebookdocumentation, invention disclosures, reduction to practice, andpatent application reviews

EQUIVALENCY STATEMENT: 1 year of higher education can be substituted for 1 year of directly related work experience(Example: bachelor's degree = 4 years of directly related work experience).

Department may hire employee at one of the following joblevels:

Biomedical Engineer, I:
Requires a bachelor's (or equivalency) + 2 years of directly related work experience or amaster's (or equivalency) degree.

• Master of Science in biomedical engineering, or a closely related engineering discipline.
• Formal training in medical device design controls.
• Experience performing risk management to ISO 14971, including hazard identification, risk analysis and verification of riskcontrols.
• Experience building and maintaining a Design History File, or an equivalent controlled design record.
• Hands-on experience prototyping and bench testing laboratory instrumentation.
• Experience supporting day to day operations of a research laboratory.
• Clear technical writing, demonstrated through reports, protocolsor standard operating procedures.

Requisition Number: PRN
46116B

Full Time or Part Time?:
Full Time

Department: 00283 - Molecular Pharmaceutics

Location:

Campus

Pay Rate Range: $48,000 to $55,000

Close Date: 11/01/2026