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Medical Device Development Jobs in Indiana (NOW HIRING)

Hearst

Medical Device Coder

Carmel, IN

$17.75 - $23.75/hr

Ability to research devices, categories, and HCPCS codes leading to the development of a library ... FDB is the leading provider of drug and medical device knowledge that helps healthcare ...

Hearst

Medical Device Coder

Carmel, IN · On-site

$17.75 - $23.75/hr

Ability to research devices, categories, and HCPCS codes leading to the development of a library ... FDB is the leading provider of drug and medical device knowledge that helps healthcare ...

Hearst Health

Medical Device Coder

Carmel, IN · On-site

$18.50 - $24.75/hr

Ability to research devices, categories, and HCPCS codes leading to the development of a library ... FDB is the leading provider of drug and medical device knowledge that helps healthcare ...

Hearst

Medical Device Coder

Indianapolis, IN · On-site

$18 - $24/hr

Medical Device In The Quality Department In Some Jobs You Take Orders. In This One, You Write ... Ability to research devices, categories, and HCPCS codes leading to the development of a library.

New

Hearst UK

Medical Device Coder

Indianapolis, IN · On-site

$18 - $24/hr

Medical Device In Quality Department In Some Jobs You Take Orders. In This One, You Write History ... Ability to research devices, categories, and HCPCS codes leading to the development of a library.

New

Hearst Health

Medical Device Coder

Indianapolis, IN · On-site

$18 - $24/hr

Medical Device In The Quality Department In Some Jobs You Take Orders. In This One, You Write ... Ability to research devices, categories, and HCPCS codes leading to the development of a library.

New

First Databank

Medical Device Coder

Indianapolis, IN · On-site

$18 - $24/hr

Ability to research devices, categories, and HCPCS codes leading to the development of a library ... FDB is the leading provider of drug and medical device knowledge that helps healthcare ...

New

Hearst

Medical Device Coder

Carmel, IN · On-site

$18.50 - $24.75/hr

Ability to research devices, categories, and HCPCS codes leading to the development of a library ... FDB is the leading provider of drug and medical device knowledge that helps healthcare ...

Hearst Communications, Inc.

Medical Device Coder

Carmel, IN · On-site

$17.75 - $23.75/hr

Ability to research devices, categories, and HCPCS codes leading to the development of a library ... FDB is the leading provider of drug and medical device knowledge that helps healthcare ...

Hearst Newspapers

Medical Device Coder

Indianapolis, IN

$18 - $24/hr

Ability to research devices, categories, and HCPCS codes leading to the development of a library ... FDB is the leading provider of drug and medical device knowledge that helps healthcare ...

Hearst

Medical Device Coder

Carmel, IN · On-site

$17.75 - $23.75/hr

Ability to research devices, categories, and HCPCS codes leading to the development of a library ... FDB is the leading provider of drug and medical device knowledge that helps healthcare ...

First Databank

Medical Device Coder

Carmel, IN · On-site

$17.75 - $23.75/hr

Ability to research devices, categories, and HCPCS codes leading to the development of a library ... FDB is the leading provider of drug and medical device knowledge that helps healthcare ...

Hearst Health

Medical Device Coder

Carmel, IN · On-site

$17.75 - $23.75/hr

Ability to research devices, categories, and HCPCS codes leading to the development of a library ... FDB is the leading provider of drug and medical device knowledge that helps healthcare ...

Hearst

Medical Device Coder

Carmel, IN · On-site

$17.75 - $23.75/hr

Ability to research devices, categories, and HCPCS codes leading to the development of a library ... FDB is the leading provider of drug and medical device knowledge that helps healthcare ...

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Showing results 1-20

All JobsMedical Device Development JobsMedical Device Development Jobs in Indiana

Medical Device Development information

See Indiana salary details

$27.6K

$50.8K

$77.1K

How much do medical device development jobs pay per year?

As of Aug 14, 2026, the average yearly pay for medical device development in Indiana is $50,830.00, according to ZipRecruiter salary data. Most workers in this role earn between $40,400.00 and $57,100.00 per year, depending on experience, location, and employer.

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

To thrive in Medical Device Development, you need expertise in engineering or life sciences, a solid understanding of regulatory requirements, and often an advanced degree such as a master's or Ph.D. in a relevant field. Familiarity with CAD software, prototyping tools, and knowledge of FDA or ISO regulatory standards is typically required. Strong problem-solving abilities, collaboration, and effective communication distinguish top professionals in this field. These skills ensure the development of safe, innovative, and compliant medical devices that meet both user needs and regulatory standards.

What is the difference between Medical Device Development vs Medical Device Quality Assurance?

AspectMedical Device DevelopmentMedical Device Quality Assurance
CredentialsEngineering degrees, certifications like RAPS or regulatory trainingQuality certifications, ISO 13485, regulatory compliance training
Work EnvironmentDesign labs, R&D teams, product development settingsManufacturing sites, quality control labs, compliance departments
Industry UsageDesigning and creating new medical devicesEnsuring devices meet quality and regulatory standards

Medical Device Development focuses on designing and creating new medical devices, involving engineering and product innovation. Medical Device Quality Assurance ensures these devices meet safety, quality, and regulatory standards through testing and compliance processes. Both roles are essential in the medical device industry but serve different functions in the product lifecycle.

What are some common challenges faced by professionals in medical device development, and how can they be addressed?

Professionals in medical device development frequently encounter challenges such as navigating complex regulatory requirements, ensuring product safety and efficacy, and managing cross-functional collaboration between engineering, clinical, and regulatory teams. Addressing these challenges requires staying updated on evolving regulations, fostering open communication among diverse team members, and implementing robust quality control processes. Proactively engaging with regulatory bodies and regularly reviewing project milestones can help streamline development and reduce the risk of costly delays.

What is medical device development?

Medical device development is the process of designing, creating, testing, and bringing medical devices to market. This process involves multiple stages, including concept development, prototyping, preclinical and clinical testing, regulatory approval, and manufacturing. The goal is to ensure that new devices are safe, effective, and meet regulatory standards before they are used by healthcare professionals or patients. Teams in medical device development often include engineers, scientists, regulatory specialists, and quality assurance professionals.
Medical Device Development jobs near you
Infographic showing various Medical Device Development job openings in Indiana as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 16% Part Time, and 6% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $50,830 per year, or $24.4 per hour.

Medical Device DHF Engineer

Prophecy Technologies

Indianapolis, IN • On-site

Full-time

Posted 18 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