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Medical Device Reporting Jobs in Indiana (NOW HIRING)

Flotec

Quality Engineer

Avon, IN · On-site

$70K - $90K/yr

Quality Engineer - Medical Device Manufacturing Company Overview Flotec is an Indianapolis-based ... reports, material review board activities, and disposition documentation. * Review and approve ...

Ompi of America Inc

Maintenance Manager

Fishers, IN · On-site

... medical device regulations. Key Responsibilities: * Maintenance Oversight: * Plan, schedule, and ... Reporting & Communication: * Prepare and present maintenance performance reports, metrics, and ...

BSI Group

... sterile medical device experience to impact patient safety and help determine which new products go to market. Technical Specialist Responsibilities: Responsible for planning, reporting and ...

BSI Prof Serv EHS West

... sterile medical device experience to impact patient safety and help determine which new products go to market. Technical Specialist Responsibilities: Responsible for planning, reporting and ...

BSI Group

Technical Specialist, Scheme Manager, Clinical Evaluation Specialist - SaMD Reports to: Technical Team Manager Location:Home Based - Global We have exciting opportunities for medical device software ...

BSI Prof Serv EHS West

Technical Specialist, Scheme Manager, Clinical Evaluation Specialist - SaMD Reports to: Technical Team Manager Location:Home Based - Global We have exciting opportunities for medical device software ...

Siri InfoSolutions Inc

Manufacturing Engineer

Warsaw, IN · On-site

$70K - $90K/yr

Medical Device Manufacturing Engineer Location: Warsaw, IN Duration: 6+ months Experience Required ... Analyzes Data and Reports Findings: Compiles and analyzes validation data, writes comprehensive ...

Marmon

NEW PRODUCT INTRODUCTION (NPI) MANAGER

Angola, IN · On-site

$157K - $162K/yr

The ideal candidate will have strong experience in medical device product development ... Supports Monthly Management Report (MMR) analysis and generation * Champion for Health, Safety and ...

Freudenberg

Project Manager

Jeffersonville, IN · On-site

... reporting. * Understanding of scientific principles and manufacturing processes used in medical device production, such as running equipment, injection molding, extrusion, catheter manufacturing, and ...

CTE Solutions

Senior Quality Engineer

Plymouth, IN · On-site

$80K - $109K/yr

Managing Direct Reports * Developing and implementing quality control procedures and guidelines ... Conform to ISO13485, 21 CFR Part 820, and medical device industry requirements * Reviewing and ...

CTE Solutions

Senior Quality Engineer

Plymouth, IN · On-site

$80K - $109K/yr

Managing Direct Reports * Developing and implementing quality control procedures and guidelines ... Conform to ISO13485, 21 CFR Part 820, and medical device industry requirements * Reviewing and ...

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Showing results 21-40

All JobsMedical Device Reporting JobsMedical Device Reporting Jobs in Indiana

Medical Device Reporting information

See Indiana salary details

$12

$18

$24

How much do medical device reporting jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for medical device reporting in Indiana is $18.67, according to ZipRecruiter salary data. Most workers in this role earn between $16.49 and $20.14 per hour, depending on experience, location, and employer.

What is the difference between Medical Device Reporting vs Medical Device Technician?

AspectMedical Device ReportingMedical Device Technician
Required CredentialsRegulatory knowledge, often a background in healthcare or regulatory affairsTechnical skills, certifications in medical equipment maintenance or biomedical technology
Work EnvironmentRegulatory agencies, healthcare compliance departmentsHospitals, clinics, biomedical equipment service centers
Employer & Industry UsageUsed by medical device manufacturers, healthcare providers, and regulatory bodiesEmployers include hospitals and biomedical service companies
Common Search & Comparison IntentUnderstanding regulatory roles in medical device safetyTechnical maintenance and repair of medical devices

Medical Device Reporting focuses on regulatory compliance and reporting adverse events, while Medical Device Technicians handle the maintenance and repair of medical equipment. Both roles are essential in the medical device industry but serve different functions within healthcare and regulatory environments.

What are the key skills and qualifications needed to thrive in medical device reporting, and why are they important?

To excel in Medical Device Reporting, you need a solid understanding of regulatory requirements, data analysis, and healthcare compliance, often supported by a degree in life sciences or a related field. Familiarity with regulatory databases such as FDA’s MAUDE, electronic reporting systems, and quality management software is typically required. Strong attention to detail, analytical thinking, and effective written communication help ensure accurate and timely reporting. These skills are critical for maintaining regulatory compliance, protecting patient safety, and supporting product quality in the medical device industry.

What are some typical challenges faced by professionals in medical device reporting, and how can they be managed?

Professionals working in Medical Device Reporting often encounter challenges such as managing tight regulatory deadlines, ensuring complete and accurate documentation, and staying current with evolving global reporting requirements. Effective time management, attention to detail, and regular training on regulatory updates are essential for success in this role. Collaboration with quality assurance, regulatory affairs, and clinical teams also helps ensure timely and compliant submissions, minimizing the risk of non-compliance.

What is medical device reporting?

Medical device reporting is the process by which manufacturers, importers, and device user facilities notify regulatory authorities, such as the FDA, about certain adverse events and product problems involving medical devices. This reporting system helps monitor the safety and effectiveness of medical devices once they are on the market. The information collected can lead to recalls, safety alerts, or other actions to protect public health.
What are popular job titles related to Medical Device Reporting jobs in Indiana? For Medical Device Reporting jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Medical Device Reporting jobs in Indiana look for? The top searched job categories for Medical Device Reporting jobs in Indiana are:
Medical Device Reporting jobs near you
Infographic showing various Medical Device Reporting job openings in Indiana as of August 2026, with employment types broken down into 87% Full Time, 5% Part Time, 5% Contract, and 3% Nights. Highlights an 100% In-person job distribution, with an average salary of $38,836 per year, or $18.7 per hour.

Postdoctoral Research Scientist - Industry Medical Device R&D

Levisonics, Inc.

Fishers, IN • On-site

Full-time

Medical, Dental, Vision, PTO

Re-posted 19 days ago

Job description

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:
  • 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

Apply