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Medical Device Rn Jobs in Florida (NOW HIRING)

Exactech

Director, Post Market

Gainesville, FL

Monitors and advises Senior Management of Medical Device regulation and standard changes to assess ... Master's Degree preferred Experience: * RN or similar healthcare certification preferred. * Minimum ...

RN Cancer Guides

Oncology Nurse Advocate

Bradenton, FL · On-site

Company Description RN Cancer Guides' mission is to provide compassionate professional oncology ... Interview patients and their loved ones to identify issues relating to their medical care * Assist ...

RN Cancer Guides

Oncology Nurse Advocate

Bradenton, FL · On-site

Company Description RN Cancer Guides' mission is to provide compassionate professional oncology ... Interview patients and their loved ones to identify issues relating to their medical care * Assist ...

RN Cancer Guides

Oncology Nurse Advocate

Inverness, FL · On-site

Company Description RN Cancer Guides' mission is to provide compassionate professional oncology ... Interview patients and their loved ones to identify issues relating to their medical care * Assist ...

Advita Ortho

Director, Post Market

Gainesville, FL · On-site

Monitors and advises Senior Management of Medical Device regulation and standard changes to assess ... Master's Degree preferred Experience: * RN or similar healthcare certification preferred. * Minimum ...

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Medical Device Rn information

See Florida salary details

$222

$1.9K

$2.9K

How much do medical device rn jobs pay per week?

As of Jun 11, 2026, the average weekly pay for medical device rn in Florida is $1,863.46, according to ZipRecruiter salary data. Most workers in this role earn between $1,451.92 and $2,255.77 per week, depending on experience, location, and employer.

What are Medical Device RNs?

Medical Device Registered Nurses (RNs) are specialized nurses who work with medical devices either in clinical settings, research, or for medical device companies. They may assist with device implementation, provide training to healthcare staff, support clinical trials, and ensure devices are used safely and effectively with patients. Their role often bridges clinical care and technology, requiring strong nursing knowledge as well as technical aptitude. Medical Device RNs may also be involved in education, troubleshooting, and regulatory compliance related to medical devices.

How does a Medical Device RN typically collaborate with engineering and product development teams?

Medical Device RNs play a crucial role in bridging clinical practice and product development. They often collaborate closely with engineers and product managers by providing clinical feedback, assisting in product testing, and ensuring devices meet regulatory and patient care standards. This collaboration may involve attending team meetings, participating in user experience studies, and helping to develop training materials. Their clinical insights help guide design improvements, making devices safer and more effective for end-users.

What are the key skills and qualifications needed to thrive as a Medical Device RN, and why are they important?

To thrive as a Medical Device RN, you need a solid nursing background (BSN or ASN) and an active RN license, along with expertise in clinical procedures related to medical devices. Familiarity with device-specific software, electronic health records (EHRs), and regulatory compliance systems like FDA guidelines is typically required. Strong communication, problem-solving, and training skills set exceptional Medical Device RNs apart, as they often educate staff and patients. These competencies ensure safe, effective integration and use of medical devices, supporting both patient outcomes and regulatory standards.

What is the difference between Medical Device Rn vs Medical Equipment Technician?

AspectMedical Device RnMedical Equipment Technician
CredentialsRegistered Nurse license, certifications in medical devicesCertification in medical equipment technology, technical training
Work EnvironmentHospitals, clinics, patient care settingsMedical equipment repair shops, hospitals, technical service centers
Employer & IndustryHealthcare providers, hospitals, clinicsMedical device companies, healthcare facilities, service providers

Medical Device Rns primarily focus on patient care, using their nursing skills to operate and troubleshoot medical devices in clinical settings. Medical Equipment Technicians specialize in repairing and maintaining medical equipment, often working in technical or repair environments. While both roles require technical knowledge of medical devices, the Medical Device Rn emphasizes patient interaction and clinical use, whereas the Medical Equipment Technician concentrates on technical maintenance and repair.

What cities in Florida are hiring for Medical Device Rn jobs? Cities in Florida with the most Medical Device Rn job openings:
Medical Device Rn jobs near you
Infographic showing various Medical Device Rn job openings in Florida as of June 2026, with employment types broken down into 10% As Needed, 63% Full Time, 24% Part Time, 2% Temporary, and 1% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $96,900 per year, or $46.6 per hour.
Director, Post Market

Director, Post Market

Exactech

Gainesville, FL

Full-time

Posted 10 days ago

Job description

 The Director Post Market Quality Assurance provides leadership and direction in ensuring the sustainability of an effective and compliant Quality Management System (QMS) Post Market QA program, that includes the following key processes: 
Post Market Surveillance 
Product Correction and Removal Program (Field Safety Notices, Recalls, etc) 
Complaint Management 
Vigilance Reporting 
MDR reporting 
Recall reporting 
EUDAMED reporting 
  • The Director of Post Market Quality Assurance is responsible to develop, lead, and direct a Quality Assurance team that manages the key post market QMS Processes indicated in the purpose section above.
  • Responsible for identifying and resourcing improvement programs to ensure suitability and compliance to all applicable Medical Device regulatory regulations and standards. 
  • Oversees the timely collection, analysis, and reporting of all post market quality signals to determine the need for escalation, correction and removal, or corrective/preventive actions. 
  • Responsible for managing communication to the FDA and international regulatory agencies for post-market surveillance activities (i.e., complaints, adverse event and incident reporting, recalls, and field safety corrective actions). 
  • Prepares inputs to the required Management Reviews per the policies and procedures established. 
  • Leads key QMS Projects that drive improvements in process efficiencies and effectiveness while assuring compliance to Medical Device Regulations. 
  • Monitors and advises Senior Management of Medical Device regulation and standard changes to assess the impact to the QMS. 
  • Provides cross functional support with other Team Leaders to implement continuous improvements projects in a timely manner. 
  • Reviews and approves applicable QMS documentation pertaining to Product Correction/Removal and post market quality processes. 
  • Provides guidance and training of GMP requirements to company employees on an annual basis. 
  • Ensure company documentation meets the required guidelines for maintaining FDA Medical Device compliance, ISO, and other applicable domestic and international regulations 
  • Facilitates cross functional collaboration in implementing post market quality related activities. 
  • Key member in supporting third party, customer and regulatory audits as required. 
  • Practice Advita's Values. 
  • Know and apply CFR Part 820 Medical Device Quality System Regulations, CFR Part 806, CFR 803 and ISO 13485:2016 requirements and any other applicable Federal and International standards. 
Education:
  •  Bachelor's Degree in a related field from an accredited institution required; Master's Degree preferred 
 Experience:
  •  RN or similar healthcare certification preferred. 
  • Minimum 10 years' experience in FDA/ISO medical devices or equivalent quality management system regulations required 
  • Minimum 5 years experience technical writing skills for healthcare, science or quality management systems required 
Functional/Technical Knowledge, Skills and Abilities Required:
  •  Working knowledge of windows-based office productivity tools including word processor and spreadsheet 
  • Excellent verbal and written communication skill 
  •  Detailed oriented with strong organizational skills 
  • Self-directed, capable of helping establish cross functional priorities and working collaboratively to meet established deadline 
  • Ability to understand, coordinate and implement technical documentation effectively with individuals and cross functional teams to improve the timely completion of projects 

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