We are a dynamic and innovative medical device startup developing a point-of-care blood coagulation ... Collaborate closely with internal engineers, external clinicians, and research partners to align ...
We are a dynamic and innovative medical device startup developing a point-of-care blood coagulation ... Collaborate closely with internal engineers, external clinicians, and research partners to align ...
Process Validation Engineer The Process Validation Engineer leads validation activities for ... Ensure all changes to equipment and processes meet medical device validation and quality standards ...
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Process Validation Engineer The Process Validation Engineer leads validation activities for ... Ensure all changes to equipment and processes meet medical device validation and quality standards ...
... Engineer (Mid Level) 100% onsite at Lakeview Office, Indianapolis, Indiana Day shift, M-F 7am to ... Understanding of validation requirements and processes applicable to the medical device industry.
... Engineer (Mid Level) 100% onsite at Lakeview Office, Indianapolis, Indiana Day shift, M-F 7am to ... Understanding of validation requirements and processes applicable to the medical device industry.
Senior Quality Engineer- Medical Device MFg
$85K - $115K/yr
Company Description TekWissen provides a unique portfolio of innovative capabilities that seamlessly combines clients insights, strategy, design, software engineering, and systems integration. www ...
Senior Quality Engineer- Medical Device MFg
$85K - $115K/yr
Company Description TekWissen provides a unique portfolio of innovative capabilities that seamlessly combines clients insights, strategy, design, software engineering, and systems integration. www ...
Manufacturing Engineer
Warsaw, IN · On-site
$70K - $90K/yr
Role : Medical Device Manufacturing Engineer Location: Warsaw, IN Duration: 6+ months Experience Required 4 - 6 years (Prior Zimmer Biomet experience is preferred) Technical/Functional Skills:
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Manufacturing Engineer
Warsaw, IN · On-site
$70K - $90K/yr
Role : Medical Device Manufacturing Engineer Location: Warsaw, IN Duration: 6+ months Experience Required 4 - 6 years (Prior Zimmer Biomet experience is preferred) Technical/Functional Skills:
Python Programing Experience * Quality Assurance and Risk Analysis. * Medical Device design experience. * Experience with a wide variety of additive manufacturing, e.g. Stratasys FDM Thermoplastics ...
Python Programing Experience * Quality Assurance and Risk Analysis. * Medical Device design experience. * Experience with a wide variety of additive manufacturing, e.g. Stratasys FDM Thermoplastics ...
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 ...
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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 ...
Validation Engineer The Validation Engineer leads process validation for automation and equipment ... Ensure that all process and equipment changes meet medical device validation and quality standards.
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Validation Engineer The Validation Engineer leads process validation for automation and equipment ... Ensure that all process and equipment changes meet medical device validation and quality standards.
Support processes for Medical Device Reporting and Complaints for Avalign as specification developer products. * Ensure required design documentation is retained in design history files and technical ...
Support processes for Medical Device Reporting and Complaints for Avalign as specification developer products. * Ensure required design documentation is retained in design history files and technical ...
Strong expertise in Medical Device Manufacturing, Smart Product Development, and R&D Engineering. * Deep understanding of the end‑to‑end product development lifecycle for medical devices and ...
New
Strong expertise in Medical Device Manufacturing, Smart Product Development, and R&D Engineering. * Deep understanding of the end‑to‑end product development lifecycle for medical devices and ...
New
Reliability Engineer II - Exempt
Warsaw, IN · On-site
$40 - $45/hr
We are seeking a skilled Reliability Engineer II to play a pivotal role in ensuring the reliability ... Must Have * 1-3 years of experience in the Medical Device industry. * Familiarity with FDA 21 CFR ...
Reliability Engineer II - Exempt
Warsaw, IN · On-site
$40 - $45/hr
We are seeking a skilled Reliability Engineer II to play a pivotal role in ensuring the reliability ... Must Have * 1-3 years of experience in the Medical Device industry. * Familiarity with FDA 21 CFR ...
QA Strategy Lead - Medical Devices & Compliance
Indianapolis, IN · On-site
$142K - $224K/yr
Merck in Indianapolis is looking for an Associate Director of Quality Engineering & Quality Assurance. This role focuses on ensuring compliance with medical device regulations and leading quality ...
New
QA Strategy Lead - Medical Devices & Compliance
Indianapolis, IN · On-site
$142K - $224K/yr
Merck in Indianapolis is looking for an Associate Director of Quality Engineering & Quality Assurance. This role focuses on ensuring compliance with medical device regulations and leading quality ...
New
Bachelor's or higher degree in a discipline relevant to the medical device industry. This may includeelectronic/electrical,electro-mechanical or biomedical engineering or medical physics.
Bachelor's or higher degree in a discipline relevant to the medical device industry. This may includeelectronic/electrical,electro-mechanical or biomedical engineering or medical physics.
Bachelor's or higher degree in a discipline relevant to the medical device industry. This may includeelectronic/electrical,electro-mechanical or biomedical engineering or medical physics.
Bachelor's or higher degree in a discipline relevant to the medical device industry. This may includeelectronic/electrical,electro-mechanical or biomedical engineering or medical physics.
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 ...
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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
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 ...
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 ...
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 ...
Medical Device Engineer information
See Indiana salary details
$20.36 - $26.87
5% of jobs
$33.13 is the 25th percentile. Wages below this are outliers.
$26.87 - $33.38
21% of jobs
$33.38 - $39.88
21% of jobs
The median wage is $42.42 / hr.
$39.88 - $46.39
9% of jobs
$46.39 - $52.90
16% of jobs
$54.53 is the 75th percentile. Wages above this are outliers.
$52.90 - $59.41
11% of jobs
$59.41 - $65.92
6% of jobs
$65.92 - $72.43
7% of jobs
$72.43 - $78.94
2% of jobs
$78.94 - $85.44
1% of jobs
$85.44 - $91.95
0% of jobs
$20
$47
$91
How much do medical device engineer jobs pay per hour?
What are the key skills and qualifications needed to thrive as a Medical Device Engineer, and why are they important?
What does a Medical Device Engineer do?
What are some common challenges Medical Device Engineers face when bringing a new product from concept to market?
What is the difference between Medical Device Engineer vs Biomedical Engineer?
| Aspect | Medical Device Engineer | Biomedical Engineer |
|---|---|---|
| Credentials | Bachelor's or Master's in Engineering, certifications in medical device design | Bachelor's or Master's in Biomedical Engineering or related field |
| Work Environment | Design, develop, test medical devices in labs or manufacturing settings | Research, develop medical equipment, or work in clinical settings |
| Industry Usage | Primarily in medical device manufacturing companies | Hospitals, research institutions, medical device companies |
Medical Device Engineers focus on designing and testing specific medical devices, ensuring compliance and safety. Biomedical Engineers have a broader scope, working on medical equipment, implants, and research. Both roles require similar credentials and often overlap in industry settings, but their primary focus differs.
What Does a Medical Device Engineer Do?
A medical device engineer is an engineering professional who develops new medical equipment and medical devices. As a medical device engineer, your work will vary depending on your area of expertise and may include biomedical research, material research and sourcing, computer-aided design work, and teaming up with doctors and patients. You also must understand the manufacturing process and ensure the products you design are both useful and cost-effective. You look for innovative solutions to medical problems and design new equipment diagnoses and treatments.
- Orthopedic Device Sales
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- Entry Level Medical Device Sales
- Internship Orthopedic Device Sales
- Freelance 1099 Medical Device Sales
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- Locum Medical Device Design
- Contract Medical Device Design
- Medical Sales Associate

Full-time
Medical, Dental, Vision, PTO
Re-posted 25 days ago
Job description
We are a dynamic and innovative medical device startup developing a point-of-care blood coagulation testing device. Our fast-growing team is passionate about transforming diagnostic testing and improving patient care. As a small, mission-driven company, we offer a collaborative environment where team members can take ownership, contribute meaningfully, and grow with us. We're looking for versatile, motivated individuals who are excited to be part of an early-stage team and make a real-world impact.
Job Summary:
We're seeking a Postdoctoral Research Scientist with a strong background in coagulation, diagnostics, and experimental research to join our core R&D team. This is a unique opportunity to contribute to the advancement of next-generation diagnostic technology in a hands-on, high-growth startup environment. The ideal candidate will bring deep scientific knowledge, creativity in study design, strong data analysis skills, and an entrepreneurial mindset.
You'll play a critical role in shaping and executing research projects, designing and running experiments, interpreting data, identifying grant opportunities, and contributing to scientific writing for grant proposals and publications. This position is ideal for someone who thrives in a fast-paced environment, loves solving hard problems, and is excited about translating scientific insight into life-changing technology.
Startup Environment:
Operating in a fast-paced startup, we value innovation, adaptability, and proactive mindsets. Ideal team members thrive under pressure, manage multiple projects, and adapt as company needs evolve. We are looking for individuals who are passionate about making a meaningful impact in the medical device industry and are excited to tackle challenges head-on.
Key Responsibilities:
- Develop and implement research plans using Levisonics' proprietary diagnostic prototypes to investigate blood coagulation dynamics.
- Design and execute experimental studies, including study planning, hypothesis generation, and experimental protocol development.
- Conduct literature reviews to support experimental design, regulatory documentation, and ongoing product development.
- Optimize protocols for accuracy, reproducibility, and compliance with ethical and regulatory standards.
- Acquire and analyze research data using statistical and bioinformatics tools; identify trends, patterns, and correlations.
- Visualize and interpret data to generate actionable insights and guide prototype improvements.
- Collaborate closely with internal engineers, external clinicians, and research partners to align scientific and technical goals.
- Identify and evaluate relevant grant opportunities (e.g., NIH, NSF, DoD) and contribute significantly to the preparation of competitive grant applications, including Specific Aims, Research Strategy, and biosketches.
- Communicate research outcomes clearly through reports, internal presentations, publications, and regulatory materials.
- Contribute to the continuous improvement of prototype functionality and experimental capabilities.
- Support cross-functional needs and take on ad-hoc tasks typical of a startup environment.
Minimum Qualifications:
- Ph.D. in Medical Sciences, Biomedical Engineering, Bioengineering, or a related field.
- Strong independent R&D experience, ideally in coagulation, hematology, trauma, or diagnostic technologies.
- Proven ability to design, execute, and interpret experiments.
- Proficiency with data analysis and visualization tools (Python, R, MATLAB, GraphPad, etc.).
- Strong scientific writing and literature review skills.
- Experience in identifying and writing grant applications.
- Prior experience with diagnostic or point-of-care device development is a plus.
- Strong communication and teamwork skills.
- Entrepreneurial mindset and ability to adapt in a fast-paced, evolving environment.
- Publication record in peer-reviewed journals.
What We Offer:
- Competitive salary
- Health, dental, and vision insurance coverage
- Generous paid time off
- Professional development opportunities
- Potential to receive stock options
- Opportunities for growth within the company
- Flexible work arrangements, including remote work options
- Dynamic and innovative startup environment
- Opportunity to make a meaningful impact in the medical device industry
About Levisonics, Inc. Created with Wix.com
Sourced by ZipRecruiter
Company size
1 - 10 Employees
Headquarters location
New Orleans, LA, US
Year founded
2016