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Medical Device Risk Management Jobs in Tennessee

Medical equipment manufacturing

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Senior Engineering Manager

Cordova, TN · On-site

Continuous Improvement & Risk Management Partner cross-functionally to deliver responsive, data ... medical device, aerospace, automotive, or similar * preferred) * 5+ years of people leadership or ...

Medical equipment manufacturing

Be Seen First

Senior Engineering Manager

Cordova, TN · On-site

Continuous Improvement & Risk Management Partner cross-functionally to deliver responsive, data ... medical device, aerospace, automotive, or similar * preferred) * 5+ years of people leadership or ...

PNC Bank

$80K - $194K/yr

Establishes the line of business risk management strategies and programs, maintains and enhances ... Depending on your eligibility, options for full-time employees include: medical/prescription drug ...

PNC Bank

$75K - $125K/yr

As a LOB Risk Specialist, Senior within PNC's Technology Third-Party Risk Management organization ... Depending on your eligibility, options for full-time employees include: medical/prescription drug ...

New

Bioventus

Sr Manager, Purchasing

Memphis, TN · On-site

... medical device environment. What you'll be doing * Develop and execute purchasing and sourcing ... Collaborates with Audit & Risk Management function to identify business risks, and develop and ...

Osv_bioventus

Sr Manager, Purchasing

Memphis, TN

... medical device environment.What you'll be doing * Develop and execute purchasing and sourcing ... Collaborates with Audit & Risk Management function to identify business risks, and develop and ...

Acadia Healthcare

Risk Coordinator

Burns, TN

$92K/yr

In this role, you will assist in executing the risk management program, lead incident ... Medical Executive Committee, and other meetings as assigned, as well as recording the minutes.

Osv_bioventus

Sr Manager, Purchasing

Memphis, TN

... medical device environment.What you'll be doing * Develop and execute purchasing and sourcing ... Collaborates with Audit & Risk Management function to identify business risks, and develop and ...

Pwc

Global Tax Risk Management- Manager

Nashville, TN

$73K - $244K/yr

... tax risk management for the entire network. As a Manager, you will inspire and develop your team ... PwC offers a wide range of benefits, including medical, dental, vision, 401k, holiday pay, vacation ...

PNC Bank

$55K - $141K/yr

Executes the Line of Business Risk Management program, identifying opportunities for enhancement ... Depending on your eligibility, options for full-time employees include: medical/prescription drug ...

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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 9, 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

Senior Engineering Manager

Medical equipment manufacturing

Cordova, TN • On-site

Full-time

Medical, Dental, Vision, Life, PTO

Posted 12 days ago

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Job description

Essential Job Functions:

Passion:

  • Passion:
  • People & Technical Leadership
  • Lead and develop Manufacturing and Quality Engineers to build strong technical capability, accountability, and engagement. Foster a culture of ownership and continuous learning while strengthening technical depth, decision-making rigor, and succession readiness.
  • Operational & Business Excellence

Champion engineering and quality excellence through disciplined execution, robust processes, and proactive risk management. Ensure engineering resources are effectively aligned to support production, NPI, CapEx, and strategic initiatives.

  • Trustworthiness:
  • Quality Leadership
  • Ensure manufacturing and quality engineering activities comply with applicable regulatory and quality system requirements (e.g., ISO 13485, FDA QSR, GxP). Serve as a trusted leader for audits, inspections, and customer quality engagements
  • Continuous Improvement & Risk Management

Partner cross-functionally to deliver responsive, data-driven engineering and quality support. Serve as the escalation point for complex process, quality, and customer issues, ensuring disciplined change management to protect quality and delivery.

  • Drive Results:
  • Problem Solving & Corrective Action
  • Lead and support root cause investigations, CAPAs, and continuous improvement initiatives to eliminate defects, reduce variation, and prevent recurrence.
  • Project & Resource Management

Prioritize and balance engineering and quality workloads to support production needs, NPI, and strategic initiatives.

  • Collaboration:
  • Cross-Functional Partnership
  • Align engineering and quality efforts with site and company objectives through strong cross-functional partnership. Lead engineering and quality execution for NPI, ensuring manufacturability, robust validation, and scalable inspection strategies.

Skills:

  • Strong people leadership and coaching capabilities
  • Deep technical expertise in machining-intensive manufacturing environments (CNC turning, Swiss lathes, CNC grinding, secondary operations) and quality inspection
  • Expertise in root cause analysis, CAPA, PFMEA, control plans, and validation
  • Strong project management, prioritization, and decision-making skills
  • Ability to interpret data, manage risk, and drive fact-based decisions
  • Excellent communication skills; ability to influence across levels and functions

Experience:

  • 8-12+ years of experience in machining-focused manufacturing engineering within a regulated or high-precision environment (medical device, aerospace, automotive, or similar
  • preferred)
  • 5+ years of people leadership or technical team leadership experience
  • Demonstrated hands-on experience with CNC machining processes, including process development, troubleshooting, and production support
  • Experience with regulated manufacturing environment and quality systems such as ISO 13485 or FDA QSR, GxP, validation protocols, and audit readiness

Education: Bachelor’s degree in Mechanical Engineering, Manufacturing Engineering, or related technical field.

  • Licenses/Certification: Certifications such as Six Sigma, Lean Manufacturing, or ASQ credentials preferred.
  • Technology/Equipment: Microsoft Office Applications and familiarity with manufacturing software systems (MES, ERP, process monitoring tools)

Physical Demands:

  • Ability to work in both office and manufacturing environments for extended periods
  • Occasional lifting and/or moving of up to 20 lbs. (fixtures, tooling, small equipment)
  • Must be able to wear Personal Protective Equipment (PPE) as required in manufacturing areas.
  • Excellent visual acuity for inspection, reading drawings, and reviewing documentation.
  • Ability to hear and communicate clearly in meetings, on calls, and during team discussions.

Working Conditions:

  • Primarily office-based with regular time spent on the production floor and in controlled manufacturing environments.
  • Standard Monday–Friday schedule, with flexibility to support production needs or project milestones.
  • Frequent interaction with manufacturing equipment, processes, and cross-functional teams

Reporting Structure:

This position reports to the Director of Engineering

Work Location: In person