ZipRecruiter

Log In

1

Manager Medical Device Software Engineer Jobs in Tennessee

Danaher

Software Engineer Internships

Jackson, TN · On-site

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 ...

Danaher

Software Engineer Internships

Knoxville, TN · On-site

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 ...

Danaher

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 ...

New

Danaher

Software Engineer Internships

Memphis, TN · On-site

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 ...

Danaher

Software Engineer Internships

Chattanooga, TN · On-site

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 ...

Danaher

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 ...

New

next page

Showing results 1-20

All JobsMedical Device Software Engineer JobsManager Medical Device Software Engineer JobsManager Medical Device Software Engineer Jobs in Tennessee

Manager Medical Device Software Engineer information

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.

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 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.
What are the most commonly searched types of Medical Device Software Engineer jobs in Tennessee? The most popular types of Medical Device Software Engineer jobs in Tennessee are:
What are popular job titles related to Manager Medical Device Software Engineer jobs in Tennessee? For Manager Medical Device Software Engineer jobs in Tennessee, the most frequently searched job titles are:
What job categories do people searching Manager Medical Device Software Engineer jobs in Tennessee look for? The top searched job categories for Manager Medical Device Software Engineer jobs in Tennessee are:
What cities in Tennessee are hiring for Manager Medical Device Software Engineer jobs? Cities in Tennessee with the most Manager Medical Device Software Engineer job openings:
Manager Medical Device Software Engineer jobs near you
Infographic showing various Manager Medical Device Software Engineer job openings in Tennessee as of July 2026, with employment types broken down into 77% Full Time, 15% Part Time, 1% Temporary, and 7% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution.
Medical Device Project Manager

Medical Device Project Manager

System One

Arlington, TN • On-site

$70 - $79/hr

Contractor

Medical, Dental, Vision, Life, Retirement

Posted 23 days ago

Job description

Job Title: Medical Device Project Manager Location: Arlington, Tennessee Type: Contract Compensation: $70.00 - $79.00 per hour Work Model: Onsite Hours: M-F 8am to 5pm

Overview Join a collaborative, fast-paced medical technology manufacturing environment where you'll lead a high-impact regulatory compliance initiative with visibility across multiple functions. This onsite Project Manager contract role offers the opportunity to drive EU MDR implementation efforts, manage project timelines, budgets, and stakeholder communications, and make a measurable impact on a critical business objective. Ideal candidates bring project management experience within the medical device industry or another highly regulated environment and thrive working independently while leading cross-functional teams.

Responsibilities

  • Lead a cross-functional team to implement the EU MDR requirements for the Arlington manufacturing site.
  • Develop and execute the project management plan, identifying risks and mitigation strategies.
  • Keep stakeholders updated on project progress.
  • Oversee plans and direct schedules as well as project budgets.
  • Monitor programs/projects from initiation through delivery, interfacing with internal customers or department personnel.
  • Organize project activities and interdepartmental meetings to ensure communication facilitates completion on schedule and within budget constraints.
  • Work independently with minimal supervision, applying professional expertise and judgment.

Requirements

  • Minimum of 4 or more years of applicable work experience in project management or related field.
  • Bachelor's Degree in Engineering or a similar field.
  • Experience within the Medical Device Industry (EU MDR) or a similar regulated environment.

System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.

System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.

Ref: #558-Scientific