We are a dynamic and innovative medical device startup developing a point-of-care blood coagulation ... Design and execute experimental studies, including study planning, hypothesis generation, and ...
Quick apply
We are a dynamic and innovative medical device startup developing a point-of-care blood coagulation ... Design and execute experimental studies, including study planning, hypothesis generation, and ...
Quick apply
We are a dynamic and innovative medical device startup developing a point-of-care blood coagulation ... Design and execute experimental studies, including study planning, hypothesis generation, and ...
We are a dynamic and innovative medical device startup developing a point-of-care blood coagulation ... Design and execute experimental studies, including study planning, hypothesis generation, and ...
We are a dynamic and innovative medical device startup developing a point-of-care blood coagulation ... Design and execute experimental studies, including study planning, hypothesis generation, and ...
Indianapolis, IN · On-site
Design Quality Engineer Technical/Functional Skills • Strong understanding of Medical Device Product Development Process and Design Control requirements. • Knowledge of FDA 21 CFR Part 820, ISO ...
Indianapolis, IN · On-site
Design Quality Engineer Technical/Functional Skills • Strong understanding of Medical Device Product Development Process and Design Control requirements. • Knowledge of FDA 21 CFR Part 820, ISO ...
Fort Wayne, IN · On-site
Viant is a global medical device partner providing design, development, manufacturing, and assembly services through capabilities in materials, plastics, metals, extrusion, and automation. With ...
Fort Wayne, IN · On-site
Viant is a global medical device partner providing design, development, manufacturing, and assembly services through capabilities in materials, plastics, metals, extrusion, and automation. With ...
Indianapolis, IN · On-site
Location: ~Indianapolis, IN~ (REMOTE) Duration: 6 months Design Quality Engineer Technical/Functional Skills • Strong understanding of Medical Device Product Development Process and Design Control ...
Indianapolis, IN · On-site
Location: ~Indianapolis, IN~ (REMOTE) Duration: 6 months Design Quality Engineer Technical/Functional Skills • Strong understanding of Medical Device Product Development Process and Design Control ...
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 ...
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 ...
Fort Wayne, IN · On-site
$800/wk
Viant is a global medical device design and manufacturing services provider that partners and innovates with customers to provide the highest quality, life enhancing medical devices. We do this ...
Fort Wayne, IN · On-site
$800/wk
Viant is a global medical device design and manufacturing services provider that partners and innovates with customers to provide the highest quality, life enhancing medical devices. We do this ...
Fort Wayne, IN · On-site
Viant is a global medical device design and manufacturing services provider that partners and innovates with customers to provide the highest quality, life enhancing medical devices. We do this ...
Fort Wayne, IN · On-site
Viant is a global medical device design and manufacturing services provider that partners and innovates with customers to provide the highest quality, life enhancing medical devices. We do this ...
Fort Wayne, IN · On-site
$800/wk
Worker is subject to noise, vibration, coolants, a #INDHP Viant is a global medical device design and manufacturing services provider that partners and innovates with customers to provide the highest ...
Fort Wayne, IN · On-site
$800/wk
Worker is subject to noise, vibration, coolants, a #INDHP Viant is a global medical device design and manufacturing services provider that partners and innovates with customers to provide the highest ...
If you have hands-on experience in the research, design, manufacture or testing of active devices we'd love to hear from you. As a Technical Reviewer, you will work with medical device manufacturers ...
If you have hands-on experience in the research, design, manufacture or testing of active devices we'd love to hear from you. As a Technical Reviewer, you will work with medical device manufacturers ...
Columbia City, IN · On-site
The Tooling Design Engineer will report directly to the Director of Operations. This position will ... is a medical device manufacturer in Columbia City, IN, specializing in surgical instruments ...
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Columbia City, IN · On-site
The Tooling Design Engineer will report directly to the Director of Operations. This position will ... is a medical device manufacturer in Columbia City, IN, specializing in surgical instruments ...
If you have hands-on experience in the research, design, manufacture or testing of active devices we'd love to hear from you. As a Technical Reviewer, you will work with medical device manufacturers ...
If you have hands-on experience in the research, design, manufacture or testing of active devices we'd love to hear from you. As a Technical Reviewer, you will work with medical device manufacturers ...
Fort Wayne, IN · On-site
$800/wk
Worker is subject to noise, vibration, coolants, a #INDHP Viant is a global medical device design and manufacturing services provider that partners and innovates with customers to provide the highest ...
Fort Wayne, IN · On-site
$800/wk
Worker is subject to noise, vibration, coolants, a #INDHP Viant is a global medical device design and manufacturing services provider that partners and innovates with customers to provide the highest ...
Jeffersonville, IN · On-site
$130K - $170K/yr
Qualifications: * 12 years of Medical Device design & development experience. * Bachelor of Science in Mechanical, Biomedical Engineering, or related discipline. Master's degree preferred. * 21CFR ...
Jeffersonville, IN · On-site
$130K - $170K/yr
Qualifications: * 12 years of Medical Device design & development experience. * Bachelor of Science in Mechanical, Biomedical Engineering, or related discipline. Master's degree preferred. * 21CFR ...
Design, evaluate, and approve packaging components and sterile packaging systems for medical device ... contract manufacturing partners. Lead sterile packaging projects by coordinating technical ...
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Design, evaluate, and approve packaging components and sterile packaging systems for medical device ... contract manufacturing partners. Lead sterile packaging projects by coordinating technical ...
IN · On-site
Design, evaluate, and approve packaging components and sterile packaging systems for medical device ... contract manufacturing partners. * Lead sterile packaging projects by coordinating technical ...
IN · On-site
Design, evaluate, and approve packaging components and sterile packaging systems for medical device ... contract manufacturing partners. * Lead sterile packaging projects by coordinating technical ...
$111K - $111K/yr
... device industry . * Demonstrated experience leading large complex programs with external and internal customers. * Technical product development experience, e.g. design, process, or quality ...
$111K - $111K/yr
... device industry . * Demonstrated experience leading large complex programs with external and internal customers. * Technical product development experience, e.g. design, process, or quality ...
IN · On-site
S.-based contract manufacturer specializing in injection molding, precision machining, cleanroom ... for the medical device industry. From concept through high-volume production, our teams work ...
IN · On-site
S.-based contract manufacturer specializing in injection molding, precision machining, cleanroom ... for the medical device industry. From concept through high-volume production, our teams work ...
Larwill, IN · On-site
S.-based contract manufacturer specializing in injection molding, precision machining, cleanroom ... for the medical device industry. From concept through high-volume production, our teams work ...
Quick apply
Larwill, IN · On-site
S.-based contract manufacturer specializing in injection molding, precision machining, cleanroom ... for the medical device industry. From concept through high-volume production, our teams work ...
Indianapolis, IN · On-site
$17 - $21.50/hr
Ability to read and interpret blueprints to determine set-up and operations Viant is a global medical device design and manufacturing services provider that partners and innovates with customers to ...
Indianapolis, IN · On-site
$17 - $21.50/hr
Ability to read and interpret blueprints to determine set-up and operations Viant is a global medical device design and manufacturing services provider that partners and innovates with customers to ...
| Aspect | Contract Medical Device Design | Medical Device Design Engineer |
|---|---|---|
| Credentials | Typically requires a degree in engineering or related field; certifications like ISO 13485 are a plus | Requires a degree in biomedical, mechanical, or electrical engineering; professional certifications may enhance prospects |
| Work Environment | Project-based, often freelance or consulting; varies by client and project scope | Full-time employment within a company or R&D department |
| Employer & Industry Usage | Used by consulting firms, contract agencies, and medical device startups | Employed by medical device companies, hospitals, or research institutions |
Contract Medical Device Design professionals focus on project-specific work, often freelance, while Medical Device Design Engineers are typically employed full-time within organizations. Both roles require similar technical credentials but differ in work setting and employment structure.
Full-time
Medical, Dental, Vision, PTO
Re-posted 21 days ago
About Us:
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:
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1 - 10 Employees
New Orleans, LA, US
2016