Radiology Software Verification Co-Op

Scorpion Therapeutics; Pennsylvania; On-site; USD 25,000 - 39,000; Full time

Job summary

Bayer's Radiology R&D team in Indianola, PA is seeking a Software Verification Engineering Co-op to support medical device development, focusing on power injector devices. The role combines hands-on test development, automation, and regulatory compliance in a highly controlled environment.

You will work with cross-functional teams to verify software against ISO 13485 and IEC 62304 standards, applying Python scripting and automated testing tools to raise product quality while learning medical

Qualifications

• Pursuing a bachelor’s in Computer, Software, Biomedical, Electrical, or Electronics Engineering.
• Strong analytical, problem-solving, communication, and teamwork skills.

Responsibilities

• Developing and automating software tests, understanding device workflows, interpreting test scenarios.
• Ensuring compliance with ISO 13485 and IEC 62304 standards.
• Collaborating with cross-functional teams on verification activities.

Skills

Analytical thinking

Problem solving

Communication

Teamwork

Education

Pursuing a bachelor’s in Computer, Software, Biomedical, Electrical, or Electronics Engineering

Tools

Python scripting

Squish

Job description

Role

Software verification engineering Co-op supporting medical device development within Bayer's regulated Radiology R&D environment, focusing on power injector devices.

Responsibilities

Developing and automating software tests, understanding device workflows, interpreting test scenarios, ensuring compliance with ISO 13485 and IEC 62304 standards, and collaborating with cross-functional teams on verification activities.

Requirements

Pursuing a bachelor's in Computer, Software, Biomedical, Electrical, or Electronics Engineering; strong analytical, problem-solving, communication, and teamwork skills.

Preferred

Proficiency in Python scripting, familiarity with automated testing tools like Squish, experience with software defect and requirements management, and awareness of medical device regulations.

High-value specifics

High-value specifics include medical device verification, software testing automation, compliance with quality standards, and working within regulated radiology device development.

Location

On-site in Indianola, PA, with full-time work; no travel specified.