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Medical Device C2C Jobs (NOW HIRING)

Concord IT Systems

$60/hr

... on C2C Experience: 10+ Years Mandatory Mandatory Skills: 510(K), SaMD, 21 CFR 11, and 21 CFR 820 ... Medical Device background. JOB PURPOSE * The Sr. Regulatory Specialist is responsible for ...

DivIHN

Software Engineer (C++/Python)

Little Canada, MN · On-site

Third-party or C2C candidates will not be considered. • We are seeking a highly skilled Software ... Security features for medical device (cardiac mapping system) • Typical Day: - Agile ceremonies ...

DivIHN Integration Inc

Sr. Systems Engineer

Pleasanton, CA · On-site

$116K - $159K/yr

Third-party or C2C candidates will not be considered. Description: Skills: * Significant experience ... Experience as a Software Systems Engineer in a Medical Device company * Experience requirements ...

DivIHN Integration Inc

Engineer I - CTQ

Skaneateles, NY · On-site

$73K - $94K/yr

Third-party or C2C candidates will not be considered. Key Responsibilities Test Protocol Development: Design and develop detailed test protocols for medical device with embedded firmware. Test ...

eNGINE LLC

Embedded Systems QA Engineer

Pittsburgh, PA · On-site

$122K - $161K/yr

Perform testing on safety-critical medical device software and associated applications * Develop ... No C2C, relocation, referral, or sponsorship candidates for this role. For finer details on how ...

MILLENNIUMSOFT

Project Manager/Analyst

Durham, NC · On-site

$105K/yr

Medical Device Company Job Category: Project Management Employment Type: Contract on W2 (Need US ... Excel analytical skills Medical background is a plus SAP Experience is a must C2C experience is a ...

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How much do medical device c2c jobs pay per hour?

As of Jun 5, 2026, the average hourly pay for medical device c2c in the United States is $36.72, according to ZipRecruiter salary data. Most workers in this role earn between $24.76 and $45.91 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Medical Device C2C (Customer-to-Customer) specialist, and why are they important?

To thrive as a Medical Device C2C specialist, you need a solid understanding of medical device products, regulatory compliance, and sales processes, often supported by a degree in life sciences or business. Familiarity with CRM software, inventory management systems, and relevant medical device regulations such as FDA or CE marking is essential. Strong interpersonal skills, negotiation abilities, and problem-solving aptitude help build trust and facilitate successful transactions between customers. These skills ensure safe, compliant, and effective exchanges of medical devices, supporting customer satisfaction and business growth.

What are some common challenges faced in a Medical Device C2C (Concept to Commercialization) role, and how can applicants prepare to address them?

Professionals in a Medical Device C2C role often encounter challenges such as navigating regulatory requirements, coordinating cross-functional teams, and managing tight project timelines. Success in this position requires excellent communication skills to align stakeholders from R&D, quality, regulatory, and marketing departments. Applicants can prepare by gaining familiarity with relevant FDA or international standards, developing project management skills, and staying current on industry trends to anticipate potential roadblocks during the product development lifecycle.

What is a Medical Device C2C?

A Medical Device C2C (Corp-to-Corp) refers to a contract arrangement where a medical device professional or consultant provides services to a client company through their own corporation or a staffing agency, rather than as a direct employee. This setup is common in the medical device industry for roles like regulatory compliance, quality assurance, or engineering. C2C contracts typically offer more flexibility and higher pay rates but require the contractor to manage their own taxes, benefits, and business expenses.

What is the difference between Medical Device C2C vs Medical Device Technician?

AspectMedical Device C2CMedical Device Technician
Required CredentialsCertification in medical device repair, technical trainingCertification or associate degree in biomedical technology or related field
Work EnvironmentContract-based, often field service or repair settingsHospital, clinic, or repair facility
Employer & Industry UsageUsed by staffing agencies, medical device companiesHospitals, medical device manufacturers, repair shops

Medical Device C2C professionals typically work as independent contractors providing repair and maintenance services, often on a contract basis. Medical Device Technicians usually work directly for healthcare facilities or manufacturers, focusing on device installation, troubleshooting, and repairs. While both roles require technical skills and certifications, C2C roles emphasize contract work, whereas technicians are employed by organizations.

Principal Software Test Engineer - 2 Openings

Principal Software Test Engineer - 2 Openings

DivIHN Integration Inc

Plymouth, MN • On-site

$142K - $191K/yr

Contractor

Posted 4 days ago

Job description

DivIHN (pronounced “divine”) is a CMMI ML3-certified Technology and Talent solutions firm. Driven by a unique Purpose, Culture, and Value Delivery Model, we enable meaningful connections between talented professionals and forward-thinking organizations. Since our formation in 2002, organizations across commercial and public sectors have been trusting us to help build their teams with exceptional temporary and permanent talent.

Visit us at https://divihn.com/find-a-job/ to learn more and view our open positions.

 
Please apply or call one of us to learn more

For further inquiries about this opportunity, please contact one of our Talent Specialists, Hema, at (630) 847-0275 or Sri Balan, at (630) 847-0953
Title: Principal Software Test Engineer - 2 Openings
Duration: 6 Months (Temp. to Perm.)
Location: Plymouth, MN

Only W2 candidates are eligible for this position. Third-party or C2C candidates will not be considered.

Job Description
The Principal Software Test Engineer leads the design, development, and execution of the software testing strategy for complex medical device systems. This role is responsible for ensuring that all software whether embedded, application level, algorithmic, or cloud connected and meets the highest standards of safety, reliability, and regulatory compliance.
The Principal Software Test Engineer functions as a technical authority in software verification, guiding cross functional teams in risk-based testing approaches and advanced test automation. This role influences technical direction without direct authority, partnering closely with Software Engineering, Systems Engineering, Quality, and Regulatory to ensure robust and compliant product development.

Key Responsibilities
Testing Strategy & Leadership
• Lead the development and execution of the overall software testing strategy for medical device products, ensuring alignment with system requirements, risk controls, and regulatory expectations.
• Drive risk based verification activities to ensure high risk features and failure modes receive appropriate coverage and depth.
• Own and maintain the verification architecture across software, hardware, and integrated system components.

Test Frameworks & Automation
• Architect, build, and scale advanced test automation frameworks to support continuous integration and continuous validation activities.
• Develop automated test solutions for unit, integration, regression, interface, and system level testing.
• Evaluate and introduce new test tools, technologies, and methods to increase efficiency, coverage, and product quality.

Technical Execution
• Design and execute verification plans, protocols, and test cases—including both manual and automated approaches.
• Review test plans, automation scripts, and documentation created by other engineers to ensure consistency, completeness, and technical accuracy.
• Lead root cause investigations, defect triage meetings, and resolution activities for software and system level issues.

Cross Functional Collaboration
• Work across engineering, quality, regulatory, and program teams to ensure verification deliverables are aligned with product goals, schedules, and compliance needs.
• Serve as a technical mentor to test engineers, providing coaching on test design, automation, documentation practices, and risk based reasoning.
• Communicate verification status, risks, and readiness with clarity to both technical and non technical stakeholders.

Compliance & Documentation
• Ensure all verification activities meet medical device software regulations and standards, including (but not limited to):
o FDA 21 CFR Part 820
o IEC 62304
o ISO 14971
o IEC 60601 1 and related standards
• Produce and maintain high quality verification documentation that supports design history files, audits, and regulatory submissions.

Required Qualifications
• Bachelor’s or Master’s degree in Software Engineering, Computer Science, Electrical Engineering, Biomedical Engineering, or related technical field.
• 10+ years of experience in software testing, verification, or validation for embedded, application level, or medical device software.
• Expertise in developing test strategies, frameworks, and automation solutions for complex, multi component systems.
• Strong programming/scripting skills (e.g., Python, C/C++, Java, C#, or similar).
• Deep understanding of software architecture, embedded systems, real time operating systems, and hardware/software interactions.
• Demonstrated experience working within regulated environments (medical device preferred).
• Proven ability to mentor engineers and influence cross functional teams without direct authority.

Preferred Qualifications
• Experience with CI/CD pipelines and test automation within Jenkins, GitLab, or equivalent environments.
• Hands on experience testing hardware integrated systems, firmware, sensors, or signal processing algorithms.
• Familiarity with cybersecurity testing, reliability testing, or networked medical device systems.
• Advanced experience authoring verification protocols, traceability matrices, and regulatory documentation.

Soft Skills & Leadership Attributes
• Strong analytical and problem solving abilities.
• Clear communicator capable of breaking down complex technical topics for diverse audiences.
• Highly organized, documentation driven, and detail oriented.
• Collaborative mindset with demonstrated ability to lead through influence.
• Passionate about safety, reliability, quality, and excellence in medical device engineering.

About us:
DivIHN, the 'IT Asset Performance Services' organization, provides Professional Consulting, Custom Projects, and Professional Resource Augmentation services to clients in the Mid-West and beyond. The strategic characteristics of the organization are Standardization, Specialization, and Collaboration.

DivIHN is an equal opportunity employer. DivIHN does not and shall not discriminate against any employee or qualified applicant on the basis of race, color, religion (creed), gender, gender expression, age, national origin (ancestry), disability, marital status, sexual orientation, or military status.