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Medical Device Risk Management Jobs in Tennessee

WilsonCTS

Project Manager - 587-1

Arlington, TN

$81/hr

... management tools and methodologies. Preferred * Experience in the medical device, healthcare, ... Risk Management * Cross-Functional Leadership * Stakeholder Management * Regulatory Compliance

TriStar Skyline Medical Center

Risk Manager

Lebanon, TN · On-site

Our TriStar Skyline Medical Center team is looking for a Risk Manager. HCA Healthcare is an advanced healthcare network that has committed up to $300 million to our incredible team members over the ...

LivaNova

Director - Product Security

Nashville, TN · On-site +1

$225K - $235K/yr

This executive will lead a dedicated team to manage the cybersecurity posture of our medical device ... Oversee a rigorous threat modeling program and lead cybersecurity risk assessments for all new and ...

Covenant Health

SR RISK MANAGER

Knoxville, TN · On-site

When risk management personnel are informed of an incident, the investigation should include getting the facts, determining the event's significance, reviewing the medical record, deciding who must ...

Covenant Health

SR RISK MANAGER

Knoxville, TN

When risk management personnel are informed of an incident, the investigation should include getting the facts, determining the event's significance, reviewing the medical record, deciding who must ...

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Showing results 1-20

All JobsMedical Device Risk Management JobsMedical Device Risk Management Jobs in Tennessee

Medical Device Risk Management information

See Tennessee salary details

$46.7K

$101.3K

$154.3K

How much do medical device risk management jobs pay per year?

As of Jun 30, 2026, the average yearly pay for medical device risk management in Tennessee is $101,250.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,700.00 and $117,100.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in Medical Device Risk Management, and why are they important?

To thrive in Medical Device Risk Management, you need a solid background in engineering or life sciences, a thorough understanding of regulatory standards (such as ISO 14971), and experience in risk assessment processes. Familiarity with risk management software, quality management systems, and relevant regulatory databases is typically required, along with certifications like Certified Risk Manager (CRM) or RAC. Strong analytical thinking, attention to detail, and effective communication are crucial soft skills for evaluating risks and collaborating with cross-functional teams. These competencies ensure the safety and compliance of medical devices, protecting both end-users and the company from regulatory or safety issues.

What is the difference between Medical Device Risk Management vs Medical Device Quality Assurance?

AspectMedical Device Risk ManagementMedical Device Quality Assurance
Primary FocusIdentifying, evaluating, and mitigating risks associated with medical devicesEnsuring products meet quality standards and regulatory requirements
CertificationsISO 14971, RAPS certifications often preferredISO 13485, regulatory compliance certifications
Work EnvironmentDesign and development teams, risk analysis meetingsManufacturing, inspection, and quality control departments
Industry UsageUsed throughout product lifecycle for safety managementUsed to maintain product quality and compliance

While both roles are essential in the medical device industry, Risk Management focuses on minimizing safety risks throughout the product lifecycle, whereas Quality Assurance ensures products consistently meet quality and regulatory standards. Understanding these differences helps professionals align their skills with industry needs.

What is medical device risk management?

Medical device risk management is the systematic process of identifying, evaluating, and controlling risks associated with medical devices throughout their lifecycle. This process ensures that potential hazards are minimized to protect patient safety and comply with regulatory standards, such as ISO 14971. Risk management includes activities like risk assessment, implementing controls, monitoring, and documenting all steps to demonstrate compliance. It is a critical function in the design, manufacturing, and post-market phases of medical device development.

How does a Medical Device Risk Management professional typically collaborate with cross-functional teams during the product development lifecycle?

Medical Device Risk Management professionals work closely with engineering, regulatory affairs, quality assurance, and clinical teams to identify, assess, and mitigate potential risks associated with medical devices. They participate in design reviews, facilitate risk assessments such as FMEA, and ensure that risk controls are effectively implemented and documented according to regulatory standards like ISO 14971. Regular communication and collaboration are essential to align risk management activities with project timelines and compliance requirements, ensuring patient safety and product success.
What are popular job titles related to Medical Device Risk Management jobs in Tennessee? For Medical Device Risk Management jobs in Tennessee, the most frequently searched job titles are:
What job categories do people searching Medical Device Risk Management jobs in Tennessee look for? The top searched job categories for Medical Device Risk Management jobs in Tennessee are:
What cities in Tennessee are hiring for Medical Device Risk Management jobs? Cities in Tennessee with the most Medical Device Risk Management job openings:
Medical Device Risk Management jobs near you
Infographic showing various Medical Device Risk Management job openings in Tennessee as of June 2026, with employment types broken down into 92% Full Time, and 8% Part Time. Highlights an 100% In-person job distribution, with an average salary of $101,250 per year, or $48.7 per hour.

Project Manager - 587-1

WilsonCTS

Arlington, TN

$81/hr

Other

Posted 4 days ago

Key responsibilities

  • Lead the planning, execution, monitoring, and successful delivery of the EU MDR implementation project.

  • Coordinate and lead cross-functional teams including Quality, Regulatory Affairs, Manufacturing, Engineering, Supply Chain, and other key stakeholders.

  • Identify project risks, develop mitigation strategies, and proactively address issues that may impact project success.

Job description

Job Title: Project Manager
Location: Tennessee, Arlington (Onsite)
Employment Type: 12 months
Pay Rate: $81/Hour

Position Overview: 
We are seeking an experienced Project Manager to lead the implementation of European Union Medical Device Regulation (EU MDR) requirements at our Arlington manufacturing site. This role will be responsible for managing a cross-functional team, developing and executing project plans, identifying and mitigating risks, and ensuring successful project delivery within established timelines and budget constraints.

The Project Manager will serve as the primary point of coordination among stakeholders, facilitating communication across departments and driving project activities from initiation through completion. This is an individual contributor role that requires strong project leadership, sound judgment, and the ability to work independently with minimal supervision.
Key Responsibilities: 
  • Lead the planning, execution, monitoring, and successful delivery of the EU MDR implementation project.
  • Develop and maintain comprehensive project management plans, schedules, milestones, and deliverables.
  • Coordinate and lead cross-functional teams including Quality, Regulatory Affairs, Manufacturing, Engineering, Supply Chain, and other key stakeholders.
  • Identify project risks, develop mitigation strategies, and proactively address issues that may impact project success.
  • Monitor project performance, timelines, budgets, and resource allocation to ensure objectives are achieved.
  • Organize and facilitate project meetings, status reviews, and stakeholder communications.
  • Provide regular project updates, reports, and recommendations to leadership and key stakeholders.
  • Ensure compliance with applicable EU MDR regulations and internal quality management system requirements.
  • Manage project documentation, change controls, and project governance processes.
  • Drive accountability among project team members and support effective decision-making throughout the project lifecycle.
  • Collaborate with internal customers and department personnel to align project goals and business objectives.
Qualifications: 
Required
  • Bachelor's degree in Business, Engineering, Life Sciences, Regulatory Affairs, Project Management, or a related field (or equivalent combination of education and experience).
  • Minimum of 4 years of project management experience leading cross-functional initiatives.
  • Experience managing projects from initiation through completion, including planning, execution, risk management, and stakeholder communication.
  • Strong organizational, analytical, and problem-solving skills.
  • Excellent verbal and written communication skills.
  • Demonstrated ability to work independently and manage multiple priorities in a fast-paced environment.
  • Proficiency with project management tools and methodologies. 
Preferred
  • Experience in the medical device, healthcare, pharmaceutical, or regulated manufacturing industry.
  • Knowledge of EU Medical Device Regulation (EU MDR) requirements.
  • Experience with regulatory compliance, quality systems, or product lifecycle management projects.
  • Project Management certification (PMP, PRINCE2, or equivalent) is a plus.
Key Competencies
  • Project Planning & Execution
  • Risk Management
  • Cross-Functional Leadership
  • Stakeholder Management
  • Regulatory Compliance
  • Budget & Resource Management
  • Change Management
  • Strategic Communication
  • Problem Solving & Decision Making
  • Attention to Detail

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