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Manager Medical Device Software Engineer Jobs in Indiana

Medical Device Coder

Carmel, IN ยท On-site

$17.75 - $23.75/hr

S. health plans, retail pharmacies, and pharmacy benefit managers; and millions of healthcare ... Partnering with our information system developer and healthcare institution customers, you'll help ...

Medical Device Coder

Carmel, IN ยท On-site

$17.75 - $23.75/hr

S. health plans, retail pharmacies, and pharmacy benefit managers; and millions of healthcare ... Partnering with our information system developer and healthcare institution customers, you'll help ...

The Software Validation Engineer will be responsible for performing validation activities as new or ... Medical device experiences a plus. Other regulated environment experience is a plus. Additional ...

We are seeking engineers with SaMD (Software as a Medical device) in technical capacity which can include product design, development and/or testing. Purpose of the position To build, manage, develop ...

We are seeking engineers with SaMD (Software as a Medical device) in technical capacity which can include product design, development and/or testing. Purpose of the position To build, manage, develop ...

Producing documentation to support medical device regulatory processes Who This Is For * Students graduating in 2026 or later with a Bachelor's degree in Computer Science, Software Engineering ...

Producing documentation to support medical device regulatory processes Who This Is For * Students graduating in 2026 or later with a Bachelor's degree in Computer Science, Software Engineering ...

Producing documentation to support medical device regulatory processes Who This Is For * Students graduating in 2026 or later with a Bachelor's degree in Computer Science, Software Engineering ...

Producing documentation to support medical device regulatory processes Who This Is For * Students graduating in 2026 or later with a Bachelor's degree in Computer Science, Software Engineering ...

Producing documentation to support medical device regulatory processes Who This Is For * Students graduating in 2026 or later with a Bachelor's degree in Computer Science, Software Engineering ...

Producing documentation to support medical device regulatory processes Who This Is For * Students graduating in 2026 or later with a Bachelor's degree in Computer Science, Software Engineering ...

Producing documentation to support medical device regulatory processes Who This Is For * Students graduating in 2026 or later with a Bachelor's degree in Computer Science, Software Engineering ...

Producing documentation to support medical device regulatory processes Who This Is For * Students graduating in 2026 or later with a Bachelor's degree in Computer Science, Software Engineering ...

Producing documentation to support medical device regulatory processes Who This Is For * Students graduating in 2026 or later with a Bachelor's degree in Computer Science, Software Engineering ...

Be Seen First

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

Be Seen First

Coordinate with production, quality, shipping, purchasing, and management to support customer needs ... Comfortable working with computers, email, Microsoft Office, and business software systems.

Showing results 21-40

Manager Medical Device Software Engineer information

What does a manager medical device software engineer do?

A Manager Medical Device Software Engineer oversees teams that design, develop, and maintain software for medical devices. They ensure that the software complies with regulatory standards, works reliably, and meets the needs of healthcare professionals and patients. In addition to technical leadership, they coordinate with cross-functional teams, manage project timelines, and mentor engineers. Their role is critical in ensuring products are both safe and effective for use in medical settings.

How does a manager medical device software engineer typically collaborate with cross-functional teams during product development?

A Manager Medical Device Software Engineer frequently works alongside teams such as regulatory affairs, quality assurance, hardware engineering, clinical specialists, and marketing. They coordinate software development activities to ensure compliance with industry standards and regulatory requirements, while also aligning software features with clinical and business needs. These managers often lead design reviews, facilitate risk assessments, and ensure effective communication between software engineers and non-technical stakeholders. This collaborative environment is essential for delivering safe, effective, and user-friendly medical devices.

What are the key skills and qualifications needed to thrive as a manager medical device software engineer, and why are they important?

To thrive as a Manager Medical Device Software Engineer, you need expertise in software development, medical device regulations (such as FDA or ISO 13485), and a background in engineering or computer science, often supported by advanced degrees or certifications. Familiarity with tools like version control systems (e.g., Git), embedded systems platforms, and quality management software is essential, along with understanding regulatory documentation processes. Strong leadership, effective communication, and problem-solving abilities distinguish top performers in this role. These skills are crucial for ensuring safe, compliant, and innovative medical device software development while leading teams to deliver high-quality products.

What are the most commonly searched types of Medical Device Software Engineer jobs in Indiana?

The most popular types of Medical Device Software Engineer jobs in Indiana are:

What are popular job titles related to Manager Medical Device Software Engineer jobs in Indiana?

For Manager Medical Device Software Engineer jobs in Indiana, the most frequently searched job titles are:

What job categories do people searching Manager Medical Device Software Engineer jobs in Indiana look for?

The top searched job categories for Manager Medical Device Software Engineer jobs in Indiana are:

What cities in Indiana are hiring for Manager Medical Device Software Engineer jobs?

Cities in Indiana with the most Manager Medical Device Software Engineer job openings:

Medical Device Coder

First Databank

Carmel, IN โ€ข On-site

$17.75 - $23.75/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 2 days ago


Job description

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

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.

ย Are you ready for this exciting challenge?ย 

____________________________________________________________________________________________

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

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:

  • Researchesย pertinent information from various sources such as manufacturers and CMS to assign the Healthcare Common Procedure Coding System (HCPCS) codes, to medical device content.ย 
  • Update andย maintainย our HCPCS library through detailed research.
  • Usesย research to develop andย maintainย HCPCS mapping andย wizard.ย 
  • Provides training to staff members.ย ย ย 
  • Ensure accuracy of codes applied to devices using data audits,ย validationsย and reviews.ย ย ย 
  • Updates HCPCS codes as changes are made to GMDN and/or UNSPSC categories.ย 
  • Evaluates current categorization schema and provides feedback and training to categorization staff.ย 
  • Evaluates medical device content to ensure the accuracy of HCPCS mappings.ย 
  • Follows up with manufacturers when code assignments are notย straightforwardย or data is inadequate, ambiguous, or unclear for coding purposes.ย 
  • Ensures updates from CMS are applied to dataย in a timely mannerย using maintenance tools.ย ย ย ย 
  • Ensuresย accuracy of codesย and codesย are current and active.ย 
  • Searches for information in cases where the coding is complex or unusual.ย 
  • Abides by the Standards of Ethical Coding as set forth by the American Health Information Management Association and adheres to official coding guidelines.ย 
  • Keeps abreast of andย complies withย coding guidelines and reimbursement reporting requirements

Required Skills:.

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

Required Experience:

  • Two years of coding experience in a healthcare setting.ย 
  • Previousย experience in supply chain management or medical device industry preferred.ย 
  • Certified Professional Coder (CPC) certification.

_____________________________________________________________________________________________

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 visitย www.fdbhealth.com or follow us onย andย 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 makeย 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 emailย 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 visitย EEO is the Law,ย EEO is the Law Supplement, ย Pay Transparency, andย 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.ย