ZipRecruiter

Log In

1

Medical Device Engineer Jobs in Indiana (NOW HIRING)

Hearst Communications, Inc.

Medical Device Coder

Carmel, IN · On-site

$17.75 - $23.75/hr

Partnering with our information system developer and healthcare institution customers, you'll help ... Evaluates medical device content to ensure the accuracy of HCPCS mappings. * Follows up with ...

Hearst Health

Medical Device Coder

Carmel, IN · On-site

$17.75 - $23.75/hr

Partnering with our information system developer and healthcare institution customers, you'll help ... Evaluates medical device content to ensure the accuracy of HCPCS mappings. * Follows up with ...

Hearst Newspapers

Medical Device Coder

Indianapolis, IN

$18 - $24/hr

Partnering with our information system developer and healthcare institution customers, you'll help ... Evaluates medical device content to ensure the accuracy of HCPCS mappings. * Follows up with ...

Hearst

Medical Device Coder

Carmel, IN · On-site

$17.75 - $23.75/hr

Partnering with our information system developer and healthcare institution customers, you'll help ... Evaluates medical device content to ensure the accuracy of HCPCS mappings. * Follows up with ...

Hearst

Medical Device Coder

Carmel, IN

$17.75 - $23.75/hr

Partnering with our information system developer and healthcare institution customers, you'll help ... Evaluates medical device content to ensure the accuracy of HCPCS mappings. * Follows up with ...

Hearst

Medical Device Coder

Carmel, IN

$17.75 - $23.75/hr

Partnering with our information system developer and healthcare institution customers, you'll help ... Evaluates medical device content to ensure the accuracy of HCPCS mappings. * Follows up with ...

First Databank

Medical Device Coder

Carmel, IN

$17.75 - $23.75/hr

Partnering with our information system developer and healthcare institution customers, you'll help ... Evaluates medical device content to ensure the accuracy of HCPCS mappings. * Follows up with ...

Hearst

Medical Device Coder

Carmel, IN

$17.75 - $23.75/hr

Partnering with our information system developer and healthcare institution customers, you'll help ... Evaluates medical device content to ensure the accuracy of HCPCS mappings. * Follows up with ...

VOLT

Medical Device Assembler

Carmel, IN · On-site

$20 - $23/hr

Come create your career with Volt Volt is immediately hiring a Medical Device Assembler in Westfield, IN 46074 As a Medical Device Assembler, you will: * Perform assembly, repair, and testing of ...

Flotec

Be Seen First

Machinist / Inspector - Medical Device Manufacturing

Avon, IN · On-site

$40K - $55K/yr

Read and interpret engineering drawings, work instructions, inspection plans, routings, and manufacturing documentation. * Verify dimensional accuracy, surface finish, threads, features, and critical ...

next page

Showing results 1-20

All JobsMedical Device Engineer JobsMedical Device Engineer Jobs in Indiana

Medical Device Engineer information

See Indiana salary details

$20

$47

$91

How much do medical device engineer jobs pay per hour?

As of Jul 31, 2026, the average hourly pay for medical device engineer in Indiana is $47.42, according to ZipRecruiter salary data. Most workers in this role earn between $33.41 and $56.73 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Medical Device Engineer, and why are they important?

To thrive as a Medical Device Engineer, you need a solid background in biomedical, mechanical, or electrical engineering, often supported by a relevant bachelor's or master's degree. Familiarity with CAD software, regulatory standards (such as FDA or ISO 13485), and design validation tools is typically required. Strong problem-solving, communication, and teamwork skills are essential for collaborating on multidisciplinary projects and ensuring product safety. These competencies are crucial for developing innovative, compliant devices that improve patient outcomes and meet rigorous industry standards.

What does a Medical Device Engineer do?

A Medical Device Engineer is responsible for designing, developing, testing, and improving medical devices used in healthcare settings. They work closely with doctors, scientists, and regulatory bodies to ensure that devices are safe, effective, and compliant with industry standards. Their work includes creating prototypes, conducting risk assessments, and overseeing the manufacturing process. Medical Device Engineers play a crucial role in bringing innovative technologies to market that help diagnose, treat, or monitor medical conditions.

What are some common challenges Medical Device Engineers face when bringing a new product from concept to market?

Medical Device Engineers often encounter challenges such as navigating complex regulatory requirements, ensuring product safety and efficacy, and coordinating with cross-functional teams including design, manufacturing, and quality assurance. Balancing innovation with compliance, managing timelines, and addressing unforeseen technical issues are also typical hurdles. Successful engineers leverage strong project management and communication skills to collaborate effectively and bring devices to market efficiently.

What is the difference between Medical Device Engineer vs Biomedical Engineer?

AspectMedical Device EngineerBiomedical Engineer
CredentialsBachelor's or Master's in Engineering, certifications in medical device designBachelor's or Master's in Biomedical Engineering or related field
Work EnvironmentDesign, develop, test medical devices in labs or manufacturing settingsResearch, develop medical equipment, or work in clinical settings
Industry UsagePrimarily in medical device manufacturing companiesHospitals, 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.

More about Medical Device Engineer jobs
What are popular job titles related to Medical Device Engineer jobs in Indiana? For Medical Device Engineer jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Medical Device Engineer jobs in Indiana look for? The top searched job categories for Medical Device Engineer jobs in Indiana are:
What cities in Indiana are hiring for Medical Device Engineer jobs? Cities in Indiana with the most Medical Device Engineer job openings:
What are popular job titles related to Medical Device Engineer jobs in IN? For Medical Device Engineer jobs in IN, the most frequently searched job titles are:
Medical Device Engineer jobs near you
Infographic showing various Medical Device Engineer job openings in Indiana as of July 2026, with employment types broken down into 77% Full Time, 15% Part Time, and 8% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $98,641 per year, or $47.4 per hour.

Medical Device DHF Engineer

Prophecy Technologies

Indianapolis, IN • On-site

Full-time

Posted 4 days ago

Job description

Role Overview:
This role focuses on supporting Design History File (DHF) activities and comprehensive risk management for medical device development projects. The specialist will be responsible for reviewing, updating, and maintaining critical documentation such as dFMEA, uFMEA, and Preliminary Hazard Analysis (PHA), ensuring compliance with regulatory and quality standards throughout the product lifecycle.
Key Responsibilities:
  • Support and manage Design History File (DHF) activities for medical device projects.
  • Review, update, and maintain Global dFMEA and uFMEA documentation, identifying and mitigating risks.
  • Develop and update Preliminary Hazard Analysis (PHA) in line with risk management procedures.
  • Support the creation and maintenance of product risk management files throughout the development lifecycle.
  • Prepare, review, and update Product Characterization documents, Product Specification Documents (PSD), and Critical-to-Quality (CTQ) documents.
  • Support the development and maintenance of Design Input, Design Output, Verification, and Validation documentation.
  • Ensure robust traceability between user needs, design inputs, risk controls, verification activities, and design outputs.
  • Collaborate cross-functionally with Design, Quality, Regulatory, Manufacturing, and Project Management teams.
  • Participate in design reviews, providing technical input on risk management and DHF compliance.
  • Support engineering change assessments and associated documentation updates.
  • Review engineering documents for completeness, accuracy, and compliance with quality system requirements.
  • Identify documentation gaps and recommend corrective actions.
  • Support audits, inspections, and compliance activities related to design control and risk management documentation.
  • Contribute to continuous improvement initiatives for product development and design control processes.
  • Ensure all deliverables comply with applicable regulatory, quality, and Zimmer Biomet procedures and standards.

Required Skills:
  • Ability to establish document traceability between User Needs, Design Inputs, Design Outputs, Risk Management, Verification, and Validation records within Cockpit Cognition.
  • Experience in supporting DHF gap assessments, document linking, metadata management, and compliance reviews.
  • Familiarity with digital DHF structure, document hierarchy, and traceability matrix development.
  • Knowledge of DHF remediation projects and legacy design documentation migration into Cockpit Cognition.
  • Strong written and verbal communication skills for project plans and inter-departmental collaboration.

Qualifications:
  • Experience in medical device development environments, particularly with Design History File (DHF) and risk management processes.

Apply