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Medical Device Manager Jobs in Indiana (NOW HIRING)

BSI Group

Build, control and manage a portfolio of Medical Device CE marking schemes focused around your area of expertise * Deliver technical reviews, scheme management in support of the CE marking schemes

BSI Prof Serv EHS West

Build, control and manage a portfolio of Medical Device CE marking schemes focused around your area of expertise * Deliver technical reviews, scheme management in support of the CE marking schemes

BSI Group

Technical Specialist & Scheme Manager - Active Devices Location: Global Homebased BSI is seeking experienced medical device professionals to join our Active Medical Devices team as a home-based ...

BSI Prof Serv EHS West

Technical Specialist & Scheme Manager - Active Devices Location: Global Homebased BSI is seeking experienced medical device professionals to join our Active Medical Devices team as a home-based ...

samtec

Senior Device Management Engineer

New Albany, IN · On-site

$96K - $132K/yr

Description Position at Samtec, Inc Senior Device Management Engineer THIS ROLE IS LOCATED ON-SITE ... medical history or genetic information, or any other status protected by applicable laws.Privacy ...

Imh

Additionally, the specialist must align tasks with a medical quality management system and have experience with healthcare and medical device regulatory, privacy, and risk management requirements.

Ompi of America Inc

Maintenance Manager

Fishers, IN · On-site

... medical device regulations. Key Responsibilities: * Maintenance Oversight: * Plan, schedule, and ... Manage spare parts inventory, maintenance budgets, and vendor relationships. * Coordinate with ...

BSI Group

To provide Medical Device expertise leadership and mentoring in areas of competence to Healthcare personnel. Key Responsibilities & Accountabilities * Plan and deliver Technical File Assessments ...

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All JobsMedical Device JobsMedical Device Manager JobsMedical Device Manager Jobs in Indiana

Medical Device Manager information

See Indiana salary details

$10

$37

$62

How much do medical device manager jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for medical device manager in Indiana is $37.53, according to ZipRecruiter salary data. Most workers in this role earn between $21.63 and $50.25 per hour, depending on experience, location, and employer.

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

To excel as a Medical Device Manager, you need a solid background in biomedical engineering, regulatory compliance, and product lifecycle management, often supported by a relevant degree and industry experience. Familiarity with quality management systems (such as ISO 13485), FDA or CE regulatory processes, and CRM or ERP software is typically required. Strong leadership, problem-solving, and communication skills help in guiding cross-functional teams and managing client relationships. These competencies ensure the safe, effective launch and maintenance of medical devices in a highly regulated market.

What is a medical device manager?

Medical Device Managers are professionals responsible for overseeing the development, production, and regulatory compliance of medical devices within healthcare organizations or manufacturing companies. They coordinate teams, manage product lifecycles, ensure products meet safety standards, and liaise with regulatory bodies such as the FDA. Their work helps ensure that medical devices are safe, effective, and brought to market efficiently. In addition, they may also handle budgeting, quality assurance, and post-market surveillance of devices.

What are some common challenges faced by medical device managers in ensuring regulatory compliance?

Medical Device Managers often encounter challenges in navigating complex and evolving regulatory requirements across different regions. Ensuring that products meet the standards set by agencies like the FDA or EMA requires continuous monitoring of changes in regulations, thorough documentation, and close collaboration with regulatory affairs and quality assurance teams. Additionally, balancing compliance with timely product development and market launch can be demanding, as even minor oversights can lead to delays or costly recalls.

What is the difference between Medical Device Manager vs Medical Equipment Coordinator?

AspectMedical Device ManagerMedical Equipment Coordinator
CertificationsRegulatory and management certifications, such as RAC or PMPBasic healthcare or equipment management certifications
Work EnvironmentHealthcare facilities, manufacturing companies, regulatory agenciesHospitals, clinics, equipment suppliers
Employer & IndustryMedical device companies, hospitals, biotech firmsHospitals, clinics, medical equipment vendors
Primary FocusOverseeing device development, compliance, and lifecycle managementManaging equipment inventory, maintenance, and distribution

The Medical Device Manager primarily focuses on overseeing the development, compliance, and lifecycle of medical devices, often requiring management certifications. In contrast, the Medical Equipment Coordinator handles equipment inventory, maintenance, and distribution within healthcare settings. Both roles are essential in healthcare but differ in scope and responsibilities.

What are the most commonly searched types of Medical Device jobs in Indiana? The most popular types of Medical Device jobs in Indiana are:
What are popular job titles related to Medical Device Manager jobs in Indiana? For Medical Device Manager jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Medical Device Manager jobs in Indiana look for? The top searched job categories for Medical Device Manager jobs in Indiana are:
What cities in Indiana are hiring for Medical Device Manager jobs? Cities in Indiana with the most Medical Device Manager job openings:
Medical Device Manager jobs near you
Infographic showing various Medical Device Manager 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 $78,062 per year, or $37.5 per hour.

Senior Software Engineer for Medical Device Startup

Levisonics Inc

Fishers, IN • On-site

$115K - $152K/yr

Full-time

Medical, Dental, Vision, PTO

Re-posted 3 days ago

Job description

About Us: 
We are a dynamic and innovative medical device startup developing a point-of-care portable blood coagulation testing device. Our full-time team currently comprises a CEO/Biomedical Engineer, and an Electrical Engineer. 

Job Summary: 
We are seeking a talented and experienced Senior Software Engineer to join our team and lead the development and optimization of software workflows for our innovative acoustic tweezing technology-based medical devices. The ideal candidate will have a Master's degree in Computer Science, Software Engineering, or a related field, with a minimum of 5 years of experience. This role requires strong coding skills in Python and C/C++, proficiency in developing intuitive and visually engaging graphical user interfaces, and expertise in SQL for effective data management and database design. Experience with version control systems, particularly Git, is essential, along with the ability to understand and generate code from workflow diagrams. As the first and only software engineer on the team, you will play a pivotal role in shaping the software development efforts for our groundbreaking technology. This role is critical to the success of our product and involves working on multiple federal grants and projects. 

Startup Environment: 
We operate in a fast-paced startup environment where innovation, adaptability, and a proactive mindset are key to success. We are looking for individuals who are passionate about working in a startup setting and thrive in dynamic and challenging situations. We value individuals who are not just seeking a job but are driven by a genuine passion for creating impactful solutions and driving change in the medical device industry. Our team members are expected to work well under pressure, juggle multiple projects, and be flexible in their roles as the needs of the company evolve. If you are excited about the opportunity to make a meaningful impact and are ready to roll up your sleeves and tackle challenges head-on, we encourage you to apply. 

Key Responsibilities: 

  1. Optimize and Enhance Existing Software: 

  • Improve the efficiency of our existing software written in Python. 

  • Increase processing speed for short-term operation on laptops. 

  • Convert and optimize the software for embedded computing devices inside the medical device long-term. 

  1. Software Packaging and Security: 

  • Secure the code to prevent reverse engineering. 

  • Package the software into executable files for easy installation and deployment. 

  1. Connectivity and Data Management: 

  • Ensure the software can connect to the internet. 

  • Implement connectivity to an online database for long-term data management. 

  • Incorporate Data Science, Machine Learning, and AI for handling large amounts of health data. 

  1. Health Data Security: 

  • Ensure the highest level of security for software and health data management. 

  1. New Technique Development: 

  • Convert and develop existing crude MATLAB codes and technology algorithms into efficient software for commercial use. 

  • Create executable files with efficient large data handling capabilities. 

  • Develop complex data processing software and manage large data analysis. 

  • Develop a user-friendly interface for healthcare professionals. 

  • Implement a remote kill switch for the software. 

  • Apply all relevant requirements from existing software. 

  1. Parallel Processing and Language Conversion: 

  • Implement efficient parallel processing techniques. 

  • Convert existing Python code to C/C++ or another suitable low-level efficient language to run software optimally on embedded hardware. 

  1. Other Responsibilities: 

  • Develop high-quality, efficient, and maintainable code. 

  • Design intuitive and visually engaging user interfaces. 

  • Proactively take on new responsibilities and suggest innovative ideas for product and company growth. 

  • Participate in grant writing and fundraising activities. 

  • Engage in FDA-related activities and adhere to quality protocols. 

  • Perform other relevant software-related tasks as needed for the company. 

Minimum Qualifications: 

  • Master’s degree in Computer Science, Software Engineering, or a related field. 

  • Minimum of 5 years of experience in software development. 

  • Strong coding skills in Python, C, and C++ (JavaScript is a plus). 

  • Proficiency in developing intuitive and visually engaging graphical user interfaces. 

  • Proficiency in SQL for effective data management and database design. 

  • Experience with version control systems, particularly Git. 

  • Ability to understand and generate code from workflow diagrams. 

  • Knowledge of integrating multiple devices and establishing centralized control. 

  • Familiarity with IDEs, preferably PyCharm. 

  • Excellent problem-solving skills and ability to work independently. 

  • Strong written and verbal communication skills. 

Preferred Qualifications: 

  • Experience working in the medical device industry. 

  • Familiarity with Agile development methodologies. 

  • Knowledge of machine learning techniques and algorithms. 

  • Experience with Docker and containerization technologies. 

  • Familiarity with cloud platforms such as AWS or Azure. 

  • Prior experience working in startups. 

  • Experience with embedded systems and medical device software development. 

  • Strong knowledge of data security, especially related to health data. 

  • Knowledge of parallel processing and algorithm optimization. 

  • Innovative mindset with a track record of proactive contributions. 

  • Experience in grant writing and regulatory compliance (FDA). 

What We Offer: 

  • Competitive salary 

  • Health, dental, and vision insurance coverage 

  • Generous paid time off 

  • Professional development opportunities 

  • Potential to receive stock options 

  • Opportunities for growth within the company 

  • Flexible work arrangements, including remote work options 

  • Dynamic and innovative startup environment 

  • Opportunity to make a meaningful impact in the medical device industry 

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