As a Software Engineering Intern at Danaher, you'll work alongside experienced engineers developing ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...
As a Software Engineering Intern at Danaher, you'll work alongside experienced engineers developing ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...
As a Software Engineering Intern at Danaher, you'll work alongside experienced engineers developing ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...
As a Software Engineering Intern at Danaher, you'll work alongside experienced engineers developing ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...
As a Software Engineering Intern at Danaher, you'll work alongside experienced engineers developing ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...
As a Software Engineering Intern at Danaher, you'll work alongside experienced engineers developing ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...
As a Software Engineering Intern at Danaher, you'll work alongside experienced engineers developing ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...
As a Software Engineering Intern at Danaher, you'll work alongside experienced engineers developing ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...
As a Software Engineering Intern at Danaher, you'll work alongside experienced engineers developing ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...
As a Software Engineering Intern at Danaher, you'll work alongside experienced engineers developing ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...
As a Software Engineering Intern at Danaher, you'll work alongside experienced engineers developing ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...
As a Software Engineering Intern at Danaher, you'll work alongside experienced engineers developing ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...
Engineer II/Manufacturing Engineer
Gary, IN · On-site
$35 - $43/hr
Gary, IN 46406 (Onsite) Duration: 6+ Months Contract Job Overview Engineer II will support manufacturing process improvements in an FDA-regulated medical device environment, following design control ...
Quick apply
Engineer II/Manufacturing Engineer
Gary, IN · On-site
$35 - $43/hr
Gary, IN 46406 (Onsite) Duration: 6+ Months Contract Job Overview Engineer II will support manufacturing process improvements in an FDA-regulated medical device environment, following design control ...
Engineering Project Coordinator
Indianapolis, IN · On-site
$60K - $65K/yr
... care, and medical device manufacturing. We partner with providers, manufacturers, and other ... The Engineering Project Coordinator plays a primary role in ensuring projects proceed according to ...
Quick apply
Engineering Project Coordinator
Indianapolis, IN · On-site
$60K - $65K/yr
... care, and medical device manufacturing. We partner with providers, manufacturers, and other ... The Engineering Project Coordinator plays a primary role in ensuring projects proceed according to ...
Engineering Project Coordinator
Indianapolis, IN · On-site
$60K - $65K/yr
... care, and medical device manufacturing. We partner with providers, manufacturers, and other ... The Engineering Project Coordinator plays a primary role in ensuring projects proceed according to ...
Quick apply
Engineering Project Coordinator
Indianapolis, IN · On-site
$60K - $65K/yr
... care, and medical device manufacturing. We partner with providers, manufacturers, and other ... The Engineering Project Coordinator plays a primary role in ensuring projects proceed according to ...
Post Market Quality Engineer
Warsaw, IN · On-site
$69K - $89K/yr
The Post Market Quality Engineer is responsible for medical device complaint investigations and write-ups as part of the Complaint Handling, Medical Device Reporting and Vigilance Reporting process.
Post Market Quality Engineer
Warsaw, IN · On-site
$69K - $89K/yr
The Post Market Quality Engineer is responsible for medical device complaint investigations and write-ups as part of the Complaint Handling, Medical Device Reporting and Vigilance Reporting process.
Quality Engineer
$65K - $84K/yr
Oversight of CMM programming schedule as directed * Participate in project management as needed ... Conform to ISO13485, 21 CFR Part 820, and medical device industry requirements * Other work-related ...
Quality Engineer
$65K - $84K/yr
Oversight of CMM programming schedule as directed * Participate in project management as needed ... Conform to ISO13485, 21 CFR Part 820, and medical device industry requirements * Other work-related ...
Quality Engineer
Plymouth, IN · On-site
$65K - $84K/yr
Oversight of CMM programming schedule as directed * Participate in project management as needed ... Conform to ISO13485, 21 CFR Part 820, and medical device industry requirements * Other work-related ...
Quality Engineer
Plymouth, IN · On-site
$65K - $84K/yr
Oversight of CMM programming schedule as directed * Participate in project management as needed ... Conform to ISO13485, 21 CFR Part 820, and medical device industry requirements * Other work-related ...
Be Seen First
Process Validation Engineer
Columbia City, IN · On-site
$20 - $25/hr
* Perform verification and validation testing activities on processes used in medical device ... Troubleshoot complex validation issues and apply advanced validation engineering and scientific ...
Quick apply
Be Seen First
Process Validation Engineer
Columbia City, IN · On-site
$20 - $25/hr
* Perform verification and validation testing activities on processes used in medical device ... Troubleshoot complex validation issues and apply advanced validation engineering and scientific ...
Quality Engineer
Noblesville, IN · On-site
$67K - $87K/yr
Quality Assurance Department: QA, Noblesville Employment Type: Full-time Req ID: 9887 We are seeking a Quality Engineer with experience in medical device design quality and risk management to support ...
Quality Engineer
Noblesville, IN · On-site
$67K - $87K/yr
Quality Assurance Department: QA, Noblesville Employment Type: Full-time Req ID: 9887 We are seeking a Quality Engineer with experience in medical device design quality and risk management to support ...
QA Risk Management Sr Engineer
Fishers, IN · On-site
$82K - $112K/yr
Description QA Risk Management Sr Engineer Summary This is an exciting opportunity to build and ... Provide QA risk management oversight for medical device and combination product (autoinjector ...
QA Risk Management Sr Engineer
Fishers, IN · On-site
$82K - $112K/yr
Description QA Risk Management Sr Engineer Summary This is an exciting opportunity to build and ... Provide QA risk management oversight for medical device and combination product (autoinjector ...
QA Risk Management Sr Engineer Summary This is an exciting opportunity to build and lead the ... Provide QA risk management oversight for medical device and combination product (autoinjector ...
QA Risk Management Sr Engineer Summary This is an exciting opportunity to build and lead the ... Provide QA risk management oversight for medical device and combination product (autoinjector ...
QA Risk Management Sr Engineer Summary This is an exciting opportunity to build and lead the ... Provide QA risk management oversight for medical device and combination product (autoinjector ...
Quick apply
QA Risk Management Sr Engineer Summary This is an exciting opportunity to build and lead the ... Provide QA risk management oversight for medical device and combination product (autoinjector ...
QA Risk Management Sr Engineer Summary This is an exciting opportunity to build and lead the ... Provide QA risk management oversight for medical device and combination product (autoinjector ...
QA Risk Management Sr Engineer Summary This is an exciting opportunity to build and lead the ... Provide QA risk management oversight for medical device and combination product (autoinjector ...
... Engineering teams to ensure excellence in assembly and compliance. What key responsibilities would you assume in this role? * Assembly Quality & Compliance Perform complex medical device assembly ...
... Engineering teams to ensure excellence in assembly and compliance. What key responsibilities would you assume in this role? * Assembly Quality & Compliance Perform complex medical device assembly ...
The Software Validation Engineer will be responsible for performing validation activities as new or ... Medical device experiences a plus. Other regulated environment experience is a plus. Additional ...
The Software Validation Engineer will be responsible for performing validation activities as new or ... Medical device experiences a plus. Other regulated environment experience is a plus. Additional ...
Intern Medical Device Engineer information
What is the difference between Intern Medical Device Engineer vs Junior Medical Device Engineer?
| Aspect | Intern Medical Device Engineer | Junior Medical Device Engineer |
|---|---|---|
| Credentials | Typically pursuing or recently completed a relevant degree | Bachelor's or Master's in biomedical, mechanical, or related engineering |
| Work Environment | Internship setting, supervised, learning-focused | Entry-level professional role, more independent tasks |
| Employer & Industry Usage | Medical device companies, research labs, internships | Medical device companies, manufacturing, R&D teams |
Intern Medical Device Engineers are usually students or recent graduates gaining hands-on experience, while Junior Medical Device Engineers are entry-level professionals with some work experience. The internship focuses on learning and support, whereas the junior role involves more responsibility in product development and testing.
What types of projects and responsibilities can an Intern Medical Device Engineer expect to be involved with during their internship?
As an Intern Medical Device Engineer, you can expect to participate in hands-on projects such as assisting in prototype development, performing laboratory testing, and collecting and analyzing data for product improvement. You'll often work closely with senior engineers, quality assurance teams, and regulatory specialists to ensure devices meet safety and compliance standards. Interns may also help prepare technical documentation and contribute to brainstorming sessions for new product features, providing a well-rounded exposure to the medical device development process. This collaborative environment offers valuable experience and networking opportunities for future career growth.
What does an Intern Medical Device Engineer do?
An Intern Medical Device Engineer assists in the design, development, and testing of medical devices under the supervision of experienced engineers. Their responsibilities may include conducting research, creating prototypes, analyzing data, and ensuring products meet regulatory standards. Interns often collaborate with cross-functional teams and gain hands-on experience in the medical device industry. This role provides valuable exposure to engineering processes and helps interns build skills required for a future career in biomedical engineering.
What are the key skills and qualifications needed to thrive as an Intern Medical Device Engineer, and why are they important?
To thrive as an Intern Medical Device Engineer, you need a solid background in biomedical engineering or a related field, along with foundational knowledge of device design and regulatory standards. Familiarity with CAD software, prototyping tools, and basic laboratory testing equipment is typically required, and coursework or certification in medical device regulations can be advantageous. Strong problem-solving, teamwork, and communication skills help interns contribute effectively to multidisciplinary projects and adapt to feedback. These competencies are crucial for ensuring safe, innovative device development and successful collaboration in a regulated industry.
What cities in Indiana are hiring for Intern Medical Device Engineer jobs? Cities in Indiana with the most Intern Medical Device Engineer job openings:
Danaher rating
7.5
Based on 27 frontline employees who took The Breakroom Quiz
Job description
How It Works
This is not an active job listing. By submitting your interest, you’ll be among the first to know when internship opportunities open at Danaher. While the roles described here reflect the types of positions we typically recruit for, we want to be transparent that specific openings have not yet been finalized. If your background aligns with future opportunities, we’ll reach out directly when formal applications become available.
About Software Engineering Roles at DanaherAre you passionate about building real-world applications, writing clean code, and solving meaningful technical challenges? As a Software Engineering Intern at Danaher, you’ll work alongside experienced engineers developing diagnostic software that powers critical healthcare tools used across the globe.
What You Might Work On- Writing and debugging code in languages such as C#, Java, Python, or C++
- Participating on an Agile Scrum team, collaborating across design, development, and testing
- Supporting the development of console and embedded software systems
- Troubleshooting issues and implementing code fixes for real product features
- Conducting peer code reviews and incorporating feedback
- Producing documentation to support medical device regulatory processes
- Students graduating in 2025 or later with a Bachelor’s degree in Computer Science, Software Engineering, Biomedical Engineering (with computational focus), or related field
- Preference for students who have completed 3+ years of coursework by the internship start date
- Experience with object-oriented programming (e.g., C#, Java, Python, C++)
- Strong analytical and debugging skills
- Comfortable working independently and in cross-functional teams
Bonus:
- Familiarity with Git or version control systems
- Knowledge of object-oriented design patterns
- Contributions to coding forums like Stack Overflow or other collaborative development communities
At Danaher, we bring together science, technology, and operational excellence to accelerate the impact of innovation in diagnostics, life sciences, and biotechnology. Our global teams work every day to solve the world’s most complex challenges by developing tools that improve human health.
As part of the Danaher family, Beckman Coulter Diagnostics is a global leader in clinical diagnostics. Together, we’re committed to creating a workplace that values inclusion, celebrates diversity, and supports career growth through mentorship and hands-on experience.
About Danaher
Sourced by ZipRecruiter
We are a science and technology innovator committed to helping our customers solve complex challenges, and improving quality of life around the world. A global family of more than 20 operating companies, we drive meaningful innovation in some of today's most dynamic, growing industries.
Industry
Medical equipment and supplies manufacturing
Company size
10,000+ Employees
Headquarters location
Washington, DC, US
Year founded
1984