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Medical Device Risk Management Jobs in Havelock, NC

Parker Boats

EHS Manager

Beaufort, NC · On-site

$73K - $99K/yr

Support organizational objectives by integrating safety, environmental stewardship, risk management ... medical incidents, environmental releases, and accident investigations • Ability to visually ...

Parker Boats

EHS Manager

Beaufort, NC · On-site

$73K - $99K/yr

... risk management, and regulatory compliance into all aspects of Parker Offshore's operations ... medical incidents, environmental releases, and accident investigations · Ability to visually ...

Parker Offshore, LLC

EHS Manager

Beaufort, NC · On-site

$73K - $99K/yr

Support organizational objectives by integrating safety, environmental stewardship, risk management ... medical incidents, environmental releases, and accident investigations Ability to visually inspect ...

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All JobsMedical Device Risk Management JobsMedical Device Risk Management Jobs in Havelock, NC

Medical Device Risk Management information

See Havelock, NC salary details

$46.1K

$99.8K

$152.1K

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

As of Aug 28, 2026, the average yearly pay for medical device risk management in Havelock, NC is $99,803.00, according to ZipRecruiter salary data. Most workers in this role earn between $80,500.00 and $115,400.00 per year, depending on experience, location, and employer.

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 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 job categories do people searching Medical Device Risk Management jobs in Havelock, NC look for?

The top searched job categories for Medical Device Risk Management jobs in Havelock, NC are:

What cities near Havelock, NC are hiring for Medical Device Risk Management jobs?

Cities near Havelock, NC with the most Medical Device Risk Management job openings:

Medical Device Risk Management jobs near you

Therapy Coordinator - Havelock, NC

LYMPHA PRESS, U.S.A.

Havelock, NC • On-site

Other

Posted 24 days ago

Job description

Advanced Lympha Press Therapy Coordinator – Havelock, NC

Part-Time | Field-Based

Position Highlights

  • Part-time, flexible schedule
  • Field-based position providing in-home patient care and education
  • Opportunity to make a direct impact on patient outcomes
  • Mission-driven healthcare organization improving patient outcomes through innovative DME solutions

Role Summary

This is a part-time, field-based role offering $125 per completed delivery (including device delivery, trial, and patient education), providing an opportunity to earn based on performance. The Advanced Lympha Press Therapy Coordinator performs in-home device deliveries, trials, and patient education within a designated geographic territory. Focusing on building strong patient relationships, this role ensures a positive customer experience while utilizing company communication and documentation technology professionally and efficiently. The Coordinator works closely with internal teams to support patient access, proper device use, and overall satisfaction.

Key Responsibilities

  • Complete Medicare Advantage trials, explaining the benefits of advanced model pumps, trialing both 51 and 52 devices, and reviewing out-of-pocket differences
  • Schedule and perform product demonstrations, including taking patient measurements and providing instructions for proper use of Lympha Press compression devices
  • Ensure patients are properly sized for correct device fit and comfort
  • Educate patients on all aspects of compression therapy devices, including garment application, prescribed protocols, and initiating therapy sessions
  • Clearly communicate patient rental agreements and financial responsibility, as well as verbal instructions to patients and caregivers based on individual needs
  • Manage and respond professionally to patient questions and concerns regarding devices or required documentation
  • Confirm scheduled appointments in advance, provide expectations for in-home visits, and organize equipment and supplies for effective patient education
  • Collaborate with internal operations teams on order completion and documentation
  • Identify, escalate, and communicate patient needs or concerns to the patient relations team for same-day follow-up whenever possible
  • Utilize company translation resources or partners to eliminate language barriers when applicable
  • Perform all duties in compliance with federal, state, accreditation, and insurance regulations, including HIPAA, non-disclosure, and non-solicitation requirements
  • Travel extensively within assigned territory to service patients and conduct in-home visits
  • Work professionally and collaboratively with other company employees, managers, and departments
  • Perform all job functions in alignment with the Company Mission, Vision, and Goal Statements

Requirements

  • High School Diploma or GED required; minimum six (6) months of related healthcare experience; professional certification or license preferred but not required
  • Previous medical device industry experience a plus
  • Strong written and verbal communication skills
  • Effective organizational, time management, and multitasking abilities
  • Knowledge of technology including scheduling, travel, and documentation applications
  • Self-motivated, self-disciplined, and able to work independently while meeting role expectations
  • Flexibility to travel to patient homes or healthcare settings for appointments
  • Ability to quickly learn and effectively use company-specific software and handheld technology tools

Physical Demands

  • Ability to lift and carry up to 60 pounds
  • Ability to sit, stand, bend, kneel, and reach as required for patient care
  • Ability to read printed materials and computer screens
  • Hearing and speech required to communicate in person and over the phone
  • Manual dexterity to perform job functions and stamina to frequently sit for extended periods

Supervisory Functions

  • This position has no supervisory responsibilities

About Lympha Press

Lympha Press helps people with lymphedema, venous disease, and lipedema improve their quality of life through innovative pneumatic compression therapy systems. We sell durable medical equipment across the United States and work closely with health plans, providers, and facilities to ensure patients have access to the products they need.

Our team works on-site at our headquarters in Glen Mills, PA, and across the country to provide exceptional service, operational excellence, and support for patient care and revenue growth.

Our mission is simple: Because Life Can Be Better. Join Lympha Press and help improve patient access and outcomes every day.

Apply Today

If you are a motivated, patient-focused professional who enjoys educating and supporting patients in their homes while ensuring proper use of medical devices, we encourage you to apply and join our Advanced Therapy team in this flexible, part-time, field-based role.

Apply