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Entry Level Biomedical Engineer Internship Jobs in Texas

MEP Engineering Intern

San Antonio, TX · On-site

$15 - $19.50/hr

Interns will be assigned a dedicated supervisor and mentor, are required to attend planned ... Conduct entry level engineering, design or drafting * Prepare engineering studies and coordinate ...

This is an entry-level position and is based out of Houston, TX. Your role * Assist in the planning ... EXPERIENCE: 0-2 years of professional experience in structural or civil engineering (internship or ...

Showing results 41-60

Entry Level Biomedical Engineer Internship information

What is the difference between Entry Level Biomedical Engineer Internship vs Biomedical Equipment Technician?

AspectEntry Level Biomedical Engineer InternshipBiomedical Equipment Technician
Required CredentialsTypically pursuing or recent graduate in biomedical engineering or related fieldAssociate's or bachelor's degree in biomedical technology or related field
Work EnvironmentResearch labs, hospitals, medical device companies, often in a learning capacityHospitals, clinics, service centers, focused on maintenance and repair
Employer & Industry UsageMedical device companies, healthcare institutions, research organizationsHospitals, healthcare facilities, medical equipment service providers

While both roles involve working with medical devices, the Entry Level Biomedical Engineer Internship focuses on gaining engineering experience and understanding device design, whereas the Biomedical Equipment Technician emphasizes hands-on maintenance and repair of medical equipment. Internships are typically temporary and educational, while technician roles are ongoing employment positions.

What are the most commonly searched types of Biomedical Engineer Internship jobs in Texas?

The most popular types of Biomedical Engineer Internship jobs in Texas are:

What cities in Texas are hiring for Entry Level Biomedical Engineer Internship jobs?

Cities in Texas with the most Entry Level Biomedical Engineer Internship job openings:

Preclinical Study Coordinator

Neuralink

Austin, TX • On-site

$31 - $53/hr

Full-time

Medical, Dental, Vision, Retirement

Re-posted 17 days ago


Job description

About Neuralink:
We are creating devices that enable a bi-directional interface with the brain. These devices allow us to restore movement to the paralyzed, restore sight to the blind, and revolutionize how humans interact with their digital world.
Team Description:
The Preclinical Team is responsible for designing, conducting, documenting, analyzing, and reporting preclinical studies. Our team provides a means for ensuring the safe, effective, and robust implantation of Neuralink devices into animals and, ultimately, humans.
Job Description and Responsibilities:
The Study Coordinator provides critical operational and project management support to the Study Director in GLP-regulated preclinical studies for Neuralink devices. This role handles the majority of day-to-day coordination, scheduling, data compilation, and administrative tasks, enabling the Study Director to focus on scientific oversight, data interpretation, and regulatory compliance. The Study Coordinator acts as a key liaison across the preclinical team, technical staff, and cross-functional groups to ensure studies progress smoothly, on time, and in compliance with protocols and SOPs. The Study Coordinator will:
  • Support the Study Director in developing study protocols, amendments, and related documentation.
  • Facilitate cross-functional communication, establish and track study timelines, and prepare/lead study milestone meetings.
  • Identify and help eliminate roadblocks that could delay study progress.
  • Assist with implementation of test methods and practices described in the study protocol and SOPs.
  • Help ensure all experimental data, including observations of unanticipated responses of the test system, are accurately recorded and verified.
  • Manage the study schedule, alerting the Study Director and team to critical data collection points or deadlines.
  • Support the documentation and addressing of self-reported or QAU-generated deviations that may affect study quality.
  • Compile data, organize contributing scientist reports, and assist in preparing the final study report so it accurately reflects study results.
  • Maintain organized study files, track communications, and support archiving of data, documentation, protocols, specimens, and reports per GLP.
  • Coordinate day-to-day study activities with technical staff, veterinary teams, and external partners (e.g., CROs if applicable).
  • Contribute to internal tracking systems, meeting minutes, and status updates for the Preclinical Team.

Required Qualifications:
  • Bachelor's degree in biology, neuroscience, biomedical engineering, animal science, or a related field.
  • Minimum 1 year of experience in preclinical research support, study coordination, or project management (academic experience applies).
  • Solid understanding of GLP regulations (21 CFR Part 58), basic knowledge of ISO 10993, and familiarity with in vivo animal studies.
  • Strong organizational and project management skills with proven ability to manage timelines and multiple priorities.
  • Excellent attention to detail and proficiency in data compilation, documentation, and Microsoft Office (or equivalent) tools.
  • Experience working in or supporting animal research facilities with IACUC protocols.

Preferred Qualifications:
  • Master's degree in biology, neuroscience, biomedical engineering, animal science, or a related field.
  • Direct experience with neural device implantation studies or neurosurgical models.
  • Background in a CRO or medical device preclinical setting.
  • Familiarity with electronic data capture systems or GLP-compliant documentation platforms.

Additional Requirements and Competencies:
  • Willingness to work in an animal research facility environment (with required training and PPE).
  • Flexibility in schedule to support critical study timepoints.

Expected Compensation:
The anticipated base salary for this position is expected to be within the following range. Your actual base pay will be determined by your job-related skills, experience, and relevant education or training. We also believe in aligning our employees' success with the company's long-term growth. As such, in addition to base salary, Neuralink offers equity compensation (in the form of Restricted Stock Units (RSU)) for all full-time employees.
Base Salary Range:
$31-$53 USD
What We Offer:
Full-time employees are eligible for the following benefits listed below.
  • An opportunity to change the world and work with some of the smartest and most talented experts from different fields
  • Growth potential; we rapidly advance team members who have an outsized impact
  • Excellent medical, dental, and vision insurance through a PPO plan
  • Paid holidays
  • Commuter benefits
  • Meals provided
  • Equity (RSUs) *Temporary Employees & Interns excluded
  • 401(k) plan *Interns initially excluded until they work 1,000 hours
  • Parental leave *Temporary Employees & Interns excluded
  • Flexible time off *Temporary Employees & Interns excluded