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Medical Device Software Engineer Jobs in Indiana

Project Engineer We are seeking a highly motivated Project Engineer to support a large-scale ... Ensure project activities meet applicable medical device regulations, quality standards, and ...

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Embedded Software Engineer

Greenwood, IN · On-site +1

$124K - $164K/yr

Embedded Software Engineer At Endress+Hauser, progress happens by working together. As the global ... Comprehensive benefit package (to include medical, dental, vision) and 401(k) savings with company ...

Embedded Software Engineer

Greenwood, IN · On-site +1

$124K - $164K/yr

Embedded Software Engineer At Endress+Hauser, progress happens by working together. As the global ... Comprehensive benefit package (to include medical, dental, vision) and 401(k) savings with company ...

Embedded Software Engineer

Greenwood, IN · On-site

$124K - $164K/yr

Embedded Software Engineer At Endress+Hauser, progress happens by working together. As the global ... Comprehensive benefit package (to include medical, dental, vision) and 401(k) savings with company ...

... device industry. This may includeelectronic/electrical,electro-mechanical or biomedical engineering ... software solutions and cyber security expertise for all industries: from aerospace and automotive ...

Manufacturing Engineer

Warsaw, IN · On-site

$70K - $90K/yr

Role : Medical Device Manufacturing Engineer Location: Warsaw, IN Duration: 6+ months Experience Required 4 - 6 years (Prior Zimmer Biomet experience is preferred) Technical/Functional Skills:

... device industry. This may includeelectronic/electrical,electro-mechanical or biomedical engineering ... software solutions and cyber security expertise for all industries: from aerospace and automotive ...

Post Market Quality Engineer

Warsaw, IN · On-site

$69K - $89K/yr

The Post Market Quality Engineer is responsible for medical device complaint investigations and ... and software tools. * Utilize applicable quality tools (Root cause analyses) to ensure timely ...

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Showing results 1-20

Medical Device Software Engineer information

See Indiana salary details

$60.4K

$140.4K

$195.5K

How much do medical device software engineer jobs pay per year?

As of Jul 13, 2026, the average yearly pay for medical device software engineer in Indiana is $140,378.00, according to ZipRecruiter salary data. Most workers in this role earn between $114,200.00 and $164,600.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Medical Device Software Engineer position, and why are they important?

To thrive as a Medical Device Software Engineer, you need a solid background in software development, embedded systems, and biomedical engineering, often supported by a degree in computer science, electrical engineering, or a related field. Experience with programming languages like C/C++, knowledge of real-time operating systems, and familiarity with medical device regulatory standards such as IEC 62304 are typically required. Strong problem-solving skills, attention to detail, and effective communication are essential soft skills for this position. These skills ensure high-quality, compliant software that contributes to safe and reliable medical devices, which are critical for patient health.

What is a Medical Device Software Engineer job?

A Medical Device Software Engineer is responsible for designing, developing, testing, and maintaining software used in medical devices. They ensure compliance with regulatory standards like FDA and IEC 62304 while working on embedded systems, user interfaces, or cloud-based healthcare applications. Their role involves collaborating with cross-functional teams, including hardware engineers and regulatory specialists, to ensure patient safety and product effectiveness.

What are some typical daily responsibilities of a Medical Device Software Engineer?

Medical Device Software Engineers typically spend their days designing, coding, and testing software for medical devices in compliance with health regulations. They collaborate closely with hardware engineers, quality assurance teams, and regulatory specialists to ensure that the software integrates seamlessly with device hardware and meets performance and safety standards. Documenting development processes, participating in code reviews, and addressing feedback from cross-functional teams are also common aspects of the role. This position often requires troubleshooting issues in both simulated and real clinical environments to ensure the reliability and safety of the device.

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

Project Engineer

Actalent

Noblesville, IN

$48.08 - $55.29/hr

Contractor

Medical, Dental, Vision, Life, Retirement, PTO

Posted 3 days ago

New


Job description

Job Title: Project Engineer
Job Description

We are seeking a highly motivated Project Engineer to support a large-scale capital equipment transfer project involving the relocation of a medical device production line. This individual will play a key role in planning, coordinating, and executing activities associated with a significant equipment transfer initiative, ensuring projects are completed on schedule, within scope, and in compliance with quality and regulatory requirements. The Project Engineer will work closely with cross-functional teams including Manufacturing Engineering, Quality, Validation, Operations, Supply Chain, and Regulatory Affairs to manage project deliverables throughout the transfer lifecycle. This role requires strong project management skills, validation exposure, and the ability to drive progress using Agile/Scrum methodologies in a regulated medical device environment.

Responsibilities

  • Lead and coordinate activities associated with the transfer of manufacturing equipment and production processes between facilities.
  • Develop and manage project plans, timelines, milestones, and deliverables to ensure successful project execution.
  • Facilitate and manage change control activities in accordance with company quality system requirements.
  • Collaborate with cross-functional stakeholders to identify project risks, dependencies, and mitigation strategies.
  • Support all phases of equipment implementation, including commissioning, qualification, validation, and production readiness activities.
  • Ensure project activities meet applicable medical device regulations, quality standards, and internal procedures.
  • Drive project execution using Agile and Scrum methodologies, facilitating project meetings, status updates, and issue resolution.
  • Coordinate documentation and approvals for validation protocols, reports, and associated project records.
  • Monitor project performance, communicate progress to leadership, and escalate issues when necessary.
  • Support continuous improvement initiatives and process optimization efforts throughout the transfer project.
Essential Skills
  • Bachelor's degree in Engineering or a related technical discipline.
  • Minimum of 3 years of project engineering or project management experience within the medical device industry.
  • Experience leading and managing engineering or capital equipment projects in a regulated environment.
  • Working knowledge of equipment qualification and validation activities, including commissioning, IQ/OQ/PQ, and process validation concepts.
  • Experience managing or participating in change control processes.
  • Strong understanding of project planning, scheduling, and execution methodologies.
  • Excellent communication and stakeholder management skills with the ability to work effectively across multiple functional groups.
  • Strong organizational, problem-solving, and decision-making abilities.
Additional Skills & Qualifications
  • Experience supporting manufacturing line transfers, equipment relocations, or site transfer projects.
  • Familiarity with Agile and Scrum project management methodologies.
  • Experience working under FDA or other regulated medical device quality systems.
  • Knowledge of risk management tools and continuous improvement methodologies.
  • Certification in Project Management, Agile, or Scrum is a plus.
Work Environment

The role involves working in a regulated medical device environment, requiring adherence to quality standards and regulatory requirements. The Project Engineer will collaborate with various departments and will utilize Agile and Scrum methodologies to manage project tasks effectively. The position demands flexibility and a proactive approach to problem-solving within a dynamic project setting.

Job Type & Location

This is a Contract position based out of Noblesville, IN.

Pay and Benefits

The pay range for this position is $48.08 - $55.29/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully onsite position in Noblesville,IN.

Application Deadline

This position is anticipated to close on Jul 24, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.


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About Actalent

Sourced by ZipRecruiter

Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We're supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.

Company size

5,001 - 10,000 Employees

Headquarters location

Hanover, MD, US

Year founded

1983

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