Biomedical Engineer – Entry Level

Virtue America; United States; Remote; USD 45,000 - 75,000; Full time

Job summary

Virtue America is seeking an Entry-Level Biomedical Engineer to support development, testing, maintenance, and improvement of medical devices and biomedical systems. You will assist with documentation, testing, troubleshooting, verification, and validation while ensuring quality and regulatory compliance.

This role is suited for recent graduates with a background in Biomedical Engineering or related fields and may involve collaboration with cross-functional teams in R&D, QA, manufacturing, and

Qualifications

• Bachelor's degree in Biomedical Engineering, Bioengineering, Mechanical Engineering, Electrical Engineering or related field.
• 0–2 years of experience; recent graduates and internships welcome.
• Basic understanding of medical devices and biomedical systems.
• Familiarity with technical documentation, data collection, and engineering analysis.
• Strong analytical and problem-solving skills; good communication and documentation.
• Proficiency in Microsoft Office applications.

Responsibilities

• Support the design, development, testing, and improvement of biomedical equipment and medical device components.
• Assist with equipment installation, troubleshooting, calibration, and performance testing.
• Support design verification and validation activities and prepare related documentation.
• Review engineering drawings, technical specifications, test procedures, and work instructions.
• Assist with risk assessments, root cause analysis, and corrective action activities.
• Prepare and maintain engineering records, test reports, SOPs, and technical documentation.
• Support equipment qualification activities, including IQ/OQ/PQ, where applicable.
• Collaborate with R&D, QA, Manufacturing, Regulatory Affairs, and Validation teams.
• Ensure engineering activities comply with FDA requirements, ISO standards, and quality procedures.
• Support design changes, process improvements, and continuous improvement initiatives.
• Assist with investigations involving equipment performance, product quality, or manufacturing issues.
• Maintain compliance with workplace safety and documentation requirements.

Skills

Analytical skills

Communication skills

Documentation skills

Problem-solving skills

Data collection

Engineering analysis

MS Office

Education

Bachelor's degree in Biomedical Engineering, Bioengineering, Mechanical Engineering, Electrical Engineering

Job description

Job Title: Biomedical Engineer – Entry Level

Location: Remote

Employment Type: Full-time

Experience: 0–2 Years

Job Summary

We are seeking an Entry-Level Biomedical Engineer to support the development, testing, maintenance, and improvement of medical devices, laboratory equipment, and biomedical systems. The ideal candidate will assist with engineering documentation, equipment testing, troubleshooting, verification, and validation activities while ensuring compliance with applicable quality and regulatory requirements.

This role is suitable for recent graduates with a background in Biomedical Engineering or a related engineering discipline who are interested in medical device development, pharmaceutical manufacturing, or life sciences engineering.

Key Responsibilities

• Support the design, development, testing, and improvement of biomedical equipment and medical device components.
• Assist with equipment installation, troubleshooting, calibration, and performance testing.
• Support design verification and validation activities and prepare related documentation.
• Review engineering drawings, technical specifications, test procedures, and work instructions.
• Assist with risk assessments, root cause analysis, and corrective action activities.
• Prepare and maintain engineering records, test reports, SOPs, and technical documentation.
• Support equipment qualification activities, including IQ/OQ/PQ, where applicable.
• Collaborate with Research and Development, Quality Assurance, Manufacturing, Regulatory Affairs, and Validation teams.
• Ensure engineering activities comply with applicable FDA requirements, ISO standards, and quality procedures.
• Support design changes, process improvements, and continuous improvement initiatives.
• Assist with investigations involving equipment performance, product quality, or manufacturing issues.
• Maintain compliance with workplace safety and documentation requirements.

Required Qualifications

• Bachelor's degree in Biomedical Engineering, Bioengineering, Mechanical Engineering, Electrical Engineering, or a related field.
• 0–2 years of experience; recent graduates and candidates with internships or academic projects are welcome.
• Basic understanding of medical devices, biomedical systems, engineering principles, and testing methods.
• Familiarity with technical documentation, data collection, and engineering analysis.
• Strong analytical, communication, documentation, and problem-solving skills.
• Proficiency in Microsoft Office applications.