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Contract Medical Device Software Engineer Jobs in Missouri

The Instore Device Platform team develops and maintains software for point of sale devices across ... Health benefits include medical, vision and dental coverage. Financial benefits include 401(k) ...

The Instore Device Platform team develops and maintains software for point of sale devices across ... Health benefits include medical, vision and dental coverage. Financial benefits include 401(k) ...

The Instore Device Platform team develops and maintains software for point of sale devices across ... Health benefits include medical, vision and dental coverage. Financial benefits include 401(k) ...

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 ...

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Contract Medical Device Software Engineer information

What are some common challenges faced by contract medical device software engineers, and how can they be addressed?

Contract Medical Device Software Engineers often encounter the challenge of rapidly adapting to new projects, technologies, and regulatory requirements unique to each client. Working within strict timelines while ensuring compliance with FDA and ISO standards can be demanding. To address these challenges, it's important to have strong communication skills, maintain thorough documentation, and stay updated on industry regulations. Collaborating closely with cross-functional teams—including quality assurance, hardware engineers, and regulatory affairs—also helps ensure project success and smooth integration into existing workflows.

What is the difference between Contract Medical Device Software Engineer vs Medical Device Software Developer?

AspectContract Medical Device Software EngineerMedical Device Software Developer
CredentialsTypically requires a degree in software engineering, biomedical engineering, or related field; certifications like ISO 13485 or FDA compliance knowledge are commonSimilar educational background; often holds certifications in medical device regulations or quality standards
Work EnvironmentContract roles in medical device companies, often project-based, with focus on compliance and validationFull-time or freelance positions within medical device firms, focusing on software development and testing
Industry UsageCommonly hired for specific projects requiring regulatory compliance and validation expertiseInvolved in ongoing software development, maintenance, and updates for medical devices

While both roles require technical expertise in medical device software, Contract Medical Device Software Engineers typically work on short-term projects with a focus on compliance and validation, whereas Medical Device Software Developers are involved in continuous software development and maintenance within the industry.

What is a contract medical device software engineer?

A Contract Medical Device Software Engineer is a software professional who is hired on a temporary or project basis to design, develop, and test software used in medical devices. They typically work with manufacturers to ensure that the software meets regulatory standards, such as those set by the FDA or ISO. Responsibilities may include creating embedded software, documenting code, and collaborating with cross-functional teams to deliver safe and effective medical products. Their expertise is crucial for developing reliable software that supports patient safety and product compliance.

What are the key skills and qualifications needed to thrive as a contract medical device software engineer?

To thrive as a Contract Medical Device Software Engineer, you need a solid background in software development (C/C++/Python), embedded systems, and knowledge of medical device regulations such as IEC 62304, typically supported by a relevant engineering degree. Familiarity with development environments, version control (e.g., Git), and tools for requirements management and verification are essential, along with any certifications in medical device software or quality systems. Strong problem-solving skills, attention to detail, and effective communication are crucial for collaborating with cross-functional teams and ensuring regulatory compliance. These skills and qualifications are vital to deliver safe, compliant, and innovative software solutions efficiently in a highly regulated and dynamic industry.
What cities in Missouri are hiring for Contract Medical Device Software Engineer jobs? Cities in Missouri with the most Contract Medical Device Software Engineer job openings:

Manager, System & Device Testing

Stereotaxis

Saint Louis, MO • On-site

Full-time

This job post has expired 1 day ago. Applications are no longer accepted.


Job description

Company Description: Stereotaxis is the global leader in innovative robotic technologies designed to enhance the treatment of arrhythmias and perform endovascular procedures. Its mission is the discovery, development and delivery of robotic systems, instruments, and information solutions for the interventional laboratory. These innovations help physicians provide unsurpassed patient care with robotic precision and safety, improved lab efficiency and productivity, and enhanced integration of procedural information.

Core components of Stereotaxis' systems have received regulatory clearance in the United States, European Union, China, Japan, Canada, and elsewhere. For more information, please visit www.stereotaxis.com. Position Summary: The Manager, System & Device Testing will manage the daily responsibilities for user documentation, device, software, and hardware testing

In conjunction with the development team, they will ensure overall quality of the products released to customers and proper documentation of the products. Essential Responsibilities: Responsible for functional management of assigned team of system and device test engineers Responsible for creation and maintenance of verification and validation plans, protocols, and reports Responsible for helping develop, and managing to, detailed project schedules Responsible for testing new products and software upgrades for release Establish standards for the testing and documentation of all products Maintaining the development and test environmentsQualifications & Skills: BS in an Engineering discipline highly preferred 5-10+ years' experience as test engineer for sterile devices, software and hardware highly preferred Experience in test method validation, fixture design & development, and statistical sampling & rationale highly preferred Experience in the development and testing of medical devices highly preferred Experience with required documentation for medical devices highly preferred Familiarity with FDA medical device regulatory guidelines and pathways highly preferred Management experience preferred Ability to communicate effectively, multi-task and manage several projects at once Legally authorized to work in the United States Work Conditions: This role is an in-office position at Stereotaxis' headquarters. Culture: Stereotaxis values steadfast integrity, intellectual excellence, responsiveness and reliability, and a dedication to constant improvement.

We take pride in the positive impact of our work and in building a collaborative and innovative work environment that embraces challenge.Qualifications & Skills: BS in an Engineering discipline highly preferred 5-10+ years' experience as test engineer for sterile devices, software and hardware highly preferred Experience in test method validation, fixture design & development, and statistical sampling & rationale highly preferred Experience in the development and testing of medical devices highly preferred Experience with required documentation for medical devices highly preferred Familiarity with FDA medical device regulatory guidelines and pathways highly preferred Management experience preferred Ability to communicate effectively, multi-task and manage several projects at once Legally authorized to work in the United States Work Conditions: This role is an in-office position at Stereotaxis' headquarters. Culture: Stereotaxis values steadfast integrity, intellectual excellence, responsiveness and reliability, and a dedication to constant improvement. We take pride in the positive impact of our work and in building a collaborative and innovative work environment that embraces challenge.