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Biomedical Engineering Internships Jobs in Indiana

Reliability Engineer I

Warsaw, IN · On-site

$98K - $124K/yr

To contribute to human welfare by application of biomedical engineering in the research, design ... Internship or co-op experience in reliability, manufacturing, or quality engineering * Exposure to ...

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Biomedical Engineering Internships information

See Indiana salary details

$39K

$90.2K

$133.2K

How much do biomedical engineering internships jobs pay per year?

As of Jun 30, 2026, the average yearly pay for biomedical engineering internships in Indiana is $90,215.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,900.00 and $110,400.00 per year, depending on experience, location, and employer.

What are the big 4 internships?

The 'big 4' internships typically refer to the most prestigious and competitive programs offered by major consulting firms: Deloitte, PricewaterhouseCoopers (PwC), Ernst & Young (EY), and KPMG. These internships provide valuable experience in consulting, audit, and advisory services, often leading to full-time positions for students pursuing degrees in business, finance, or related fields.

What are the key skills and qualifications needed to thrive in the Biomedical Engineering Internships position, and why are they important?

Successful Biomedical Engineering interns typically have a background in biomedical engineering or a related field, with strong analytical, problem-solving, and laboratory skills. Familiarity with software such as MATLAB, CAD tools, and basic knowledge of medical device regulations is often expected. Strong communication, teamwork, and adaptability help interns collaborate effectively with researchers, clinicians, and engineers. These skills are vital to contribute to real-world healthcare technology projects and gain valuable hands-on experience.

What is a Biomedical Engineering Internships job?

A Biomedical Engineering Internship is a temporary position that allows students or recent graduates to gain hands-on experience in the field of biomedical engineering. Interns typically work alongside professionals to assist in research, design, testing, and development of medical devices, equipment, or healthcare technologies. These internships can take place in hospitals, research labs, medical device companies, or government agencies. They provide valuable industry exposure, technical skill development, and networking opportunities that can enhance career prospects.

What are good internships for biomedical engineering?

Good internships for biomedical engineering include positions at medical device companies, research labs, and healthcare technology firms that offer hands-on experience with device design, prototyping, and regulatory processes. These internships often require knowledge of engineering principles, CAD software, and basic biology or physiology, providing valuable industry exposure and skill development.

What are 5 related careers to biomedical engineers?

Related careers to biomedical engineers include clinical engineers, biomedical equipment technicians, research scientists in biomedical fields, quality assurance specialists in medical device companies, and regulatory affairs specialists. These roles often require knowledge of medical devices, engineering principles, and compliance standards, and they involve working in healthcare, research, or manufacturing environments.

Can a biomedical engineer make 200k?

Biomedical engineering internships are typically entry-level positions that do not pay salaries close to $200,000. Experienced biomedical engineers working in senior roles, management, or specialized fields such as medical device development or regulatory affairs may reach or exceed this salary level, especially with advanced degrees and certifications. However, starting salaries for interns are generally much lower.

What types of projects or tasks do Biomedical Engineering interns typically work on during their internship?

Biomedical Engineering interns often assist with research and development of medical devices, perform laboratory experiments, analyze data, and support ongoing projects related to healthcare technology innovation. They may help with product testing, documentation, literature reviews, and process improvements under the guidance of experienced engineers or scientists. Interns usually collaborate closely with multidisciplinary teams, including clinicians, regulatory specialists, and product designers, which provides exposure to the full life cycle of biomedical product development. These experiences help interns develop a deeper understanding of the biomedical engineering field and build valuable professional skills for future career advancement.

What cities in Indiana are hiring for Biomedical Engineering Internships jobs? Cities in Indiana with the most Biomedical Engineering Internships job openings:
Infographic showing various Biomedical Engineering Internships job openings in Indiana as of June 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $90,215 per year, or $43.4 per hour.
Reliability Engineer I

Reliability Engineer I

Medtronic

Warsaw, IN • On-site

$98K - $124K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 8 days ago


Key responsibilities

  • Lead validation activities for new product launches, including development of Master Validation Plans.

  • Develop and execute equipment and process qualifications, including protocol creation and final reporting.

  • Conduct risk assessments and analyze validation and process performance data to ensure processes meet defined requirements.


Medtronic rating

7.8

Company rating: 7.8 out of 10

Based on 169 frontline employees who took The Breakroom Quiz

171st of 527 rated manufacturers


Job description

We anticipate the application window for this opening will close on - 29 Jun 2026
At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.
A Day in the Life
Are you passionate about ensuring product performance and reliability in a highly regulated manufacturing environment? At Medtronic's Warsaw, Indiana site - a global hub for orthopedic innovation - you'll play a key role in supporting reliability efforts for life-impacting medical devices. As a Reliability Engineer I, you'll partner cross-functionally to evaluate designs, analyze performance data, and support continuous improvement initiatives.
To contribute to human welfare by application of biomedical engineering in the research, design, manufacture, and sale of instruments or appliances that alleviate pain, restore health, and extend life. That's the Medtronic Mission - our compass that guides what we do every day. The Medtronic Mission sets the expectations of our culture. Every person here plays a role in bringing it to life. We recognize your potential to ensure patients live better, healthier lives.
At Medtronic, we bring bold ideas forward with speed and decisiveness to put patients first in everything we do. In-person exchanges are invaluable to our work. We're working a minimum of 5 days a week onsite as part of our commitment to fostering a culture of professional growth and cross-functional collaboration as we work together to engineer the extraordinary
In this role, you'll build foundational experience applying reliability engineering principles in a fast-paced setting, supporting testing strategies, risk assessments, and data-driven decisions to ensure products meet quality and regulatory standards.
Responsibilities may include the following and other duties may be assigned.
  • Lead validation activities in support of new product launches, including development of Master Validation Plans (MVPs)

  • Develop and execute equipment and process qualifications (IQ/OQ/PQ), including protocol creation and final reporting

  • Evaluate prior validation work to determine opportunities to leverage existing data and identify gaps requiring new validation

  • Partner cross-functionally with Manufacturing, Quality, and R&D to ensure alignment on validation strategy and execution

  • Conduct risk assessments (e.g., PFMEA) and incorporate findings into validation plans and process controls

  • Analyze validation and process performance data to ensure processes are capable, stable, and meet defined requirements

  • Manage multiple concurrent validation projects in a fast-paced new product introduction (NPI) environment

  • Ensure all validation activities are compliant with internal quality systems and applicable regulatory standards

  • Identify and implement improvements to strengthen manufacturing processes and support long-term scalability

  • Provide regular updates on validation progress, risks, and timelines to stakeholders and leadership

Minimum Requirements
  • Requires a Bachelor's degree and 0 years relevant experience.

Nice To Have
  • Internship or co-op experience in reliability, manufacturing, or quality engineering

  • Exposure to reliability principles (e.g., life testing, basic failure analysis, Weibull)

  • Experience with data analysis tools such as Minitab or JMP

  • Familiarity with risk management tools (e.g., FMEA)

  • Basic understanding of validation or testing in a regulated environment (IQ/OQ/PQ)

  • Exposure to Lean or continuous improvement methodologies

For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A) is required.
Physical Job Requirements
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.
The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role.
U.S. Work Authorization & Sponsorship
At Medtronic, we are committed to fostering an environment where employees can thrive and make a meaningful impact. In alignment with our enterprise-wide workforce planning approach, U.S. work authorization sponsorship (H-1B, TN, J, etc.) is offered exclusively for Principal-level roles and above, where specialized expertise aligns with long-term business needs. Roles below the Principal level require candidates to possess unrestricted U.S. work authorization at the time of hire and for the duration of employment.
Join us in our mission to alleviate pain, restore health, and extend life-where your unique background and perspective are valued.
Benefits & Compensation
Medtronic offers a competitive Salary and flexible Benefits Package
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
Salary ranges for U.S (excl. PR) locations (USD):$69,600.00 - $104,400.00
This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).
The base salary range is applicable across the United States, excluding Puerto Rico and specific locations in California. The offered rate complies with federal and local regulations and may vary based on factors such as experience, certification/education, market conditions, and location. Compensation and benefits information pertains solely to candidates hired within the United States (local market compensation and benefits will apply for others).
The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program).
The following benefits and additional compensation are available to all regular employees: Incentive plans, 401(k) plan plus employer contribution and match, Short-term disability, Paid time off, Paid holidays, Employee Stock Purchase Plan, Employee Assistance Program, Non-qualified Retirement Plan Supplement (subject to IRS earning minimums), and Capital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums).
Regular employees are those who are not temporary, such as interns. Temporary employees are eligible for paid sick time, as required under applicable state law, and the Employee Stock Purchase Plan. Please note some of the above benefits may not apply to workers in Puerto Rico.
Further details are available at the link below:
Medtronic benefits and compensation plans
About Medtronic
We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission - to alleviate pain, restore health, and extend life - unites a global team of 95,000+ passionate people.
We are engineers at heart- putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.
Learn more about our business, mission, and our commitment to diversity here.
It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.
If you are applying to perform work for Medtronic, Inc. ("Medtronic") in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. Medtronic will consider for employment qualified job applicants with arrest or conviction records in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.

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