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Medical Device Product Development Jobs in Indiana

Marmon

NEW PRODUCT INTRODUCTION (NPI) MANAGER

Angola, IN

$157K - $162K/yr

The ideal candidate will have strong experience in medical device product development, manufacturing operations, project management, and cross-functional leadership within a regulated environment.

Zimmer, Inc.

Senior Development Engineer II

Warsaw, IN · On-site

... medical device products in order to further Zimmer Biomet's mission and grow Zimmer Biomet's market leadership position. How You'll Create Impact * Stays current with and understands relevant product ...

VOLT

Medical Device Assembler

Carmel, IN · On-site

$20 - $23/hr

Accurately complete paper and electronic documentation to maintain full product traceability and ... Prior experience as a Medical Device Assembler or Production Assembler is required * Ability to ...

Hearst Communications, Inc.

Medical Device Coder

Carmel, IN · On-site

$17.75 - $23.75/hr

Productive. Committed. Willing and able to go above and beyond. Passionate about making a ... Ability to research devices, categories, and HCPCS codes leading to the development of a library.

Hearst

Medical Device Coder

Carmel, IN

$17.75 - $23.75/hr

Productive. Committed. Willing and able to go above and beyond. Passionate about making a ... Ability to research devices, categories, and HCPCS codes leading to the development of a library.

Hearst

Medical Device Coder

Carmel, IN

$17.75 - $23.75/hr

Productive. Committed. Willing and able to go above and beyond. Passionate about making a ... Ability to research devices, categories, and HCPCS codes leading to the development of a library.

Hearst Health

Medical Device Coder

Carmel, IN · On-site

$17.75 - $23.75/hr

Productive. Committed. Willing and able to go above and beyond. Passionate about making a ... Ability to research devices, categories, and HCPCS codes leading to the development of a library.

Hearst Newspapers

Medical Device Coder

Indianapolis, IN

$18 - $24/hr

Productive. Committed. Willing and able to go above and beyond. Passionate about making a ... Ability to research devices, categories, and HCPCS codes leading to the development of a library.

Hearst

Medical Device Coder

Carmel, IN · On-site

$17.75 - $23.75/hr

Productive. Committed. Willing and able to go above and beyond. Passionate about making a ... Ability to research devices, categories, and HCPCS codes leading to the development of a library.

Hearst

Medical Device Coder

Carmel, IN · On-site

$17.75 - $23.75/hr

Productive. Committed. Willing and able to go above and beyond. Passionate about making a ... Ability to research devices, categories, and HCPCS codes leading to the development of a library.

First Databank

Medical Device Coder

Carmel, IN

$17.75 - $23.75/hr

Productive. Committed. Willing and able to go above and beyond. Passionate about making a ... Ability to research devices, categories, and HCPCS codes leading to the development of a library.

Flotec

Be Seen First

Machinist / Inspector - Medical Device Manufacturing

Avon, IN · On-site

$40K - $55K/yr

Machinist / Inspector - Medical Device Manufacturing Company Overview Flotec is an Indianapolis ... We manufacture precision medical products including oxygen regulators, flowmeters, fittings, valves ...

Zimmer, Inc.

Development Engineer II

Warsaw, IN · On-site

... medical device products in order to further Zimmer Biomet's mission and grow Zimmer Biomet's market leadership position. How You'll Create Impact * Stay current with and understand relevant ...

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Showing results 1-20

All JobsMedical Device Product Development JobsMedical Device Product Development Jobs in Indiana

Medical Device Product Development information

See Indiana salary details

$40.4K

$120.8K

$137.5K

How much do medical device product development jobs pay per year?

As of Aug 4, 2026, the average yearly pay for medical device product development in Indiana is $120,837.00, according to ZipRecruiter salary data. Most workers in this role earn between $109,000.00 and $136,100.00 per year, depending on experience, location, and employer.

What is a medical device product development?

A Medical Device Product Development job involves designing, testing, and bringing medical devices to market while ensuring compliance with regulatory standards. Professionals in this role work with cross-functional teams, including engineering, regulatory affairs, and manufacturing, to develop safe and effective healthcare solutions. They oversee the entire product lifecycle, from concept and prototyping to clinical validation and commercialization. Strong knowledge of FDA, ISO, and other regulatory requirements is essential.

What are some typical challenges faced in medical device product development roles?

Professionals in Medical Device Product Development often encounter challenges such as navigating complex regulatory requirements, managing cross-functional project teams, and ensuring that products meet both clinical needs and quality standards. Balancing innovative design with safety and compliance can require careful planning and solid problem-solving skills. Additionally, adapting to shifting project timelines and incorporating stakeholder feedback are common aspects of the job. Overcoming these challenges is rewarding and helps ensure the delivery of safe, effective devices to patients and healthcare providers.

What are the key skills and qualifications needed to thrive in medical device product development?

To thrive in Medical Device Product Development, you need a strong background in engineering or life sciences, product design, and an understanding of regulatory requirements like FDA and ISO standards. Proficiency with CAD software, project management tools, and knowledge of quality management systems (QMS) is commonly required, along with certifications such as Six Sigma or PMP being beneficial. Strong problem-solving abilities, collaboration skills, and effective communication are key soft skills for this role. These skills are important to ensure that devices are developed safely, efficiently, and in compliance with industry regulations while fostering innovation and teamwork.

What are the most commonly searched types of Medical Device Product Development jobs in Indiana? The most popular types of Medical Device Product Development jobs in Indiana are:
What are popular job titles related to Medical Device Product Development jobs in Indiana? For Medical Device Product Development jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Medical Device Product Development jobs in Indiana look for? The top searched job categories for Medical Device Product Development jobs in Indiana are:
What cities in Indiana are hiring for Medical Device Product Development jobs? Cities in Indiana with the most Medical Device Product Development job openings:
Medical Device Product Development jobs near you
Infographic showing various Medical Device Product Development job openings in Indiana as of July 2026, with employment types broken down into 57% Full Time, and 43% Contract. Highlights an 100% In-person job distribution, with an average salary of $120,837 per year, or $58.1 per hour.

Design Quality Engineer

Prophecy Technologies

Indianapolis, IN • On-site, Remote

Full-time

Posted 6 days ago

Job description

Role Overview:
The Design Quality Engineer will play a crucial role in supporting quality activities throughout the medical device product development lifecycle. This position requires a strong understanding of Design Control requirements and regulatory standards such as FDA 21 CFR Part 820, ISO 13485, and ISO 14971, ensuring compliance and maintaining Design History File (DHF) documentation and risk management processes.
Key Responsibilities:
  • Support quality activities throughout the product development lifecycle.
  • Review and maintain Design History File (DHF) documentation for compliance with regulatory and quality requirements.
  • Lead and support risk management activities including dFMEA, uFMEA, and PHA updates.
  • Ensure traceability between User Needs, Design Inputs, Risk Controls, Verification, Validation, and Design Outputs.
  • Support Design Verification and Validation planning, execution, and documentation reviews.
  • Review Product Characterization, Product Specification (PSD), and CTQ documents.
  • Participate in design reviews and ensure compliance with Design Control processes.
  • Support Cockpit Cognition DHF Build activities, including documentation organization and traceability linkages.
  • Conduct DHF gap assessments and support remediation activities.
  • Collaborate with R&D, Manufacturing, Regulatory Affairs, and Supplier Quality teams.
  • Support CAPA investigations, root cause analysis, and implementation of corrective actions.
  • Ensure compliance with FDA, ISO 13485, ISO 14971, and internal quality procedures.
  • Support internal audits, customer audits, and regulatory inspections.
  • Drive continuous improvement initiatives related to design quality and risk management processes.

Required Skills:
  • Strong understanding of Medical Device Product Development Process and Design Control requirements.
  • Knowledge of FDA 21 CFR Part 820, ISO 13485, ISO 14971, and applicable regulatory standards.
  • Strong knowledge of Design Controls and medical device product development.
  • Experience with Design History File (DHF) development, review, and remediation.
  • Hands-on experience with Risk Management activities including: dFMEA, uFMEA, Preliminary Hazard Analysis (PHA).
  • Experience with Design Verification and Validation (V&V).
  • Understanding of User Needs, Design Inputs, Design Outputs, and Traceability requirements.
  • Experience preparing and reviewing: Product Specification Documents (PSD), Product Characterization documents, CTQ (Critical-to-Quality) documents.
  • Experience with CAPA, Nonconformance, and root cause investigations.
  • Familiarity with PLM systems such as Windchill or Teamcenter.
  • Experience with Cockpit Cognition DHF Build and DHF traceability management.
  • Strong documentation, technical writing, and audit support skills.

Qualifications:
  • Strong understanding of Medical Device Product Development Process and Design Control requirements.
  • Knowledge of FDA 21 CFR Part 820, ISO 13485, ISO 14971, and applicable regulatory standards.

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