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Medical Device Quality Jobs in Indiana (NOW HIRING)

Are you ready for this exciting challenge? _____ First Databank (FDB) is currently seeking a Medical Device in the Quality department. This position is responsible for researching data published from ...

Are you ready for this exciting challenge? _____ First Databank (FDB) is currently seeking a Medical Device in the Quality department. This position is responsible for researching data published from ...

Are you ready for this exciting challenge? _____ First Databank (FDB) is currently seeking a Medical Device in the Quality department. This position is responsible for researching data published from ...

Are you ready for this exciting challenge? _____ First Databank (FDB) is currently seeking a Medical Device in the Quality department. This position is responsible for researching data published from ...

Quality Engineer

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 ...

Quality Engineer

Noblesville, IN · On-site

$60 - $80/hr

We are seeking a Quality Engineer with experience in medical device design quality and risk management to support product development from concept through commercialization. This role will primarily ...

New

The ideal candidate has an engineering background , strong analytical and communication skills, and foundational knowledge of quality engineering concepts within a manufacturing or medical device ...

New

Showing results 41-60

Medical Device Quality information

See Indiana salary details

$20

$34

$67

How much do medical device quality jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for medical device quality in Indiana is $34.94, according to ZipRecruiter salary data. Most workers in this role earn between $23.56 and $43.70 per hour, depending on experience, location, and employer.

What is medical device quality?

Medical Device Quality refers to the processes and standards used to ensure that medical devices are safe, effective, and comply with regulatory requirements throughout their lifecycle. Professionals in this field oversee quality management systems, conduct inspections, manage documentation, and ensure that products meet both company and government standards. Their work helps prevent defects, maintains patient safety, and supports compliance with agencies like the FDA and ISO standards.

What does a medical device quality professional do?

Professionals in Medical Device Quality are typically responsible for ensuring that products meet regulatory standards and company quality requirements. Daily tasks often include reviewing and updating quality documentation, conducting audits, analyzing data from quality tests, and collaborating with manufacturing and engineering teams to resolve any issues. They also play a key role in managing non-conformances, implementing corrective actions, and supporting continuous improvement initiatives. Regular communication with regulatory bodies and staying updated on compliance requirements are also common aspects of the role.

What are the key skills and qualifications needed to thrive as a medical device quality professional?

To thrive as a Medical Device Quality professional, you need expertise in quality assurance, regulatory compliance (such as FDA and ISO 13485), and strong analytical skills, typically backed by a degree in engineering or a related field. Familiarity with quality management systems (QMS), risk management tools, and validation processes is essential, as are certifications like ASQ CQE or Six Sigma. Attention to detail, problem-solving, and effective communication are critical soft skills for ensuring product safety and collaborating across teams. These competencies help ensure that medical devices meet stringent regulatory standards and maintain patient safety and company reputation.

What is the difference between Medical Device Quality vs Medical Device Regulatory Affairs?

AspectMedical Device QualityMedical Device Regulatory Affairs
CertificationsISO 13485, Six Sigma, CQERegulatory affairs certifications, RAC, ISO 13485 familiarity
Work EnvironmentQuality departments, manufacturing sites, labsRegulatory agencies, corporate offices, compliance teams
Industry UsageEnsures product quality, compliance with standardsManages regulatory submissions, compliance with laws

Medical Device Quality focuses on maintaining product standards and compliance through quality management systems, while Medical Device Regulatory Affairs handles regulatory submissions and ensures products meet legal requirements. Both roles are essential in bringing safe, compliant medical devices to market, but they emphasize different aspects of the product lifecycle.

What cities in Indiana are hiring for Medical Device Quality jobs?

Cities in Indiana with the most Medical Device Quality job openings:

Infographic showing various Medical Device Quality job openings in Indiana as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 13% Part Time, and 5% Contract. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $72,685 per year, or $34.9 per hour.

Medical Coder Specialist

Hearst

Carmel, IN • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 18 days ago


Hearst rating

6.8

Company rating: 6.8 out of 10

Based on 27 frontline employees who took The Breakroom Quiz

51st of 78 rated media


Job description

In Some Jobs You Take Orders. In This One, You Write History. 

Join the healthcare information technology team that's turning drug and medical device data into knowledge used by thousands of hospitals; the majority of U.S. health plans, retail pharmacies, and pharmacy benefit managers; and millions of healthcare decision makers throughout the world. Partnering with our information system developer and healthcare institution customers, you'll help evolve leading-edge thinking into reality and make a measurable difference in improving human health.

We're looking for people who are: Intelligent. Productive. Committed. Willing and able to go above and beyond. Passionate about making a difference. Innovative. Energized. And want to play an essential role in a successful company's continued growth.

 Are you ready for this exciting challenge? 

____________________________________________________________________________________________

First Databank (FDB) is currently seeking a Medical Device in the Quality department. This position is responsible for researching data published from the FDA, device manufactures, and other credible sources to generate unbiased, robust medical device content for our device solution with an emphasis on HCPCS coding for medical devices. 

This position is based out of our Carmel office and follows a hybrid work model, with an expectation to work onsite at least three days per week.

Responsibilities:

  • Researches pertinent information from various sources such as manufacturers and CMS to assign the Healthcare Common Procedure Coding System (HCPCS) codes, to medical device content. 
  • Update and maintain our HCPCS library through detailed research.
  • Uses research to develop and maintain HCPCS mapping and wizard. 
  • Provides training to staff members.   
  • Ensure accuracy of codes applied to devices using data audits, validations and reviews.   
  • Updates HCPCS codes as changes are made to GMDN and/or UNSPSC categories. 
  • Evaluates current categorization schema and provides feedback and training to categorization staff. 
  • Evaluates medical device content to ensure the accuracy of HCPCS mappings. 
  • Follows up with manufacturers when code assignments are not straightforward or data is inadequate, ambiguous, or unclear for coding purposes. 
  • Ensures updates from CMS are applied to data in a timely manner using maintenance tools.    
  • Ensures accuracy of codes and codes are current and active. 
  • Searches for information in cases where the coding is complex or unusual. 
  • Abides by the Standards of Ethical Coding as set forth by the American Health Information Management Association and adheres to official coding guidelines. 
  • Keeps abreast of and complies with coding guidelines and reimbursement reporting requirements

Required Skills:.

  • Ability to research devices, categories, and HCPCS codes leading to the development of a library.
  • Expertise in oral and written communications -ability to clarify and discuss coding issues with peers. 
  • Able to multi-task and prioritize tasks.
  • Good written and verbal communication skills. 
  • Attention for detail and strong organizational skills. 
  • Medical terminology and coding.
  • Ability to use web based and computer applications and work with peers in team situations.
  • Takes initiative in performing additional tasks.
  • Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency. 
  • Skilled in developing structured prompts and reusable AI-assisted workflows to compare source data, identify inconsistencies, summarize research findings, and support coding-related decision making. 
  • Demonstrates responsible use of AI by validating all AI-generated outputs against credible sources, official coding guidance, internal standards, and professional judgment. 
  • Maintains compliance with data privacy, company security policies, ethical coding standards, and appropriate human oversight when using AI tools. 

Relevant Experience:

  • Minimum of 2-3 years of medical coding experience in a healthcare setting, including outpatient clinics, ambulatory surgical centers (ASCs), home health, or Durable Medical Equipment (DME) settings.
  • Experience assigning or auditing HCPCS Level II code sections, including A-codes, C-codes, or E-codes. 
  • Experience reviewing or resolving Medicare and Medicaid claim denials involving medical necessity, unlisted HCPCS codes, or Medically Unlikely Edits (MUEs).
  • Experience researching and applying Medicare Local Coverage Determinations (LCDs) and National Coverage Determinations (NCDs).
  • Previous experience in supply chain management or medical device industry preferred. 
  • Active coding certification from AAPC or AHIMA. Relevant credentials include: Certified Professional Coder (CPC) certification, Certified Outpatient Coder (COC), or Certified Coding Specialist (CCS).

_____________________________________________________________________________________________

About FDB:

FDB is the leading provider of drug and medical device knowledge that helps healthcare professionals make precise decisions. With thousands of customers worldwide, FDB enables our information system developer partners to deliver valuable, useful, and differentiated solutions. We offer more than three decades of experience in transforming medical knowledge into actionable, targeted, and effective solutions that help improve patient safety, operational efficiency, and healthcare outcomes. For a complete look at our solutions and services, please visit www.fdbhealth.com or follow us on and LinkedIn.

We value Integrity, Respect, Responsibility, Teamwork, and Creativity. Our offices in South San Francisco and Indianapolis have been awarded with Top Workplaces honors by The Bay Area News Group and the Indy Star, since 2016 (the Top Workplaces honors are based solely on the results of an employee feedback survey by a leading research firm that specializes in organizational health and workplace improvement). FDB offers competitive salaries and extensive benefits - including medical, dental, vision, long term disability, life insurance, and matching 401k.
We are an Equal opportunity employer - vets/disabled. We do not discriminate in hiring on the basis of sex, gender identity, sexual orientation, race, color, religious creed, national origin, physical or mental disability, protected Veteran status, or any other characteristic protected by federal, state, or local law.

First Databank, Inc. (FDB) endeavors to make www.fdbhealth.com accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please email accommodations@fdbhealth.com. This contact information is for accommodation requests only and cannot be used to inquire about the status of applications.

For more information about our commitment to equal employment opportunity, please visit EEO is the Law, EEO is the Law Supplement,  Pay Transparency, and FDB EEO/AA Statement.

In accordance with applicable law, Hearst is required to include a reasonable estimate of the compensation for this role if hired in Carmel, IN. The reasonable estimate is $47,000 to $57,000. Please note this information is specific to those hired in location. If this role is open to candidates outside of location, the salary range would be aligned to that specific location. A final decision on the successful candidate's starting salary will be based on a number of permissible, non-discriminatory factors, including but not limited to skills and experience, training, certifications, and education.

This role is also eligible for a competitive benets package that includes medical, dental, vision, life, and disability insurance; 401(k) retirement plan; exible spending savings account; paid holidays; paid time off; employee assistance program; and other company benets. 


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