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Internship Medical Device Testing Jobs in Florida

Advita Ortho

Design Engineer, Packaging

Gainesville, FL · On-site

$122K/yr

Manager, End of Line Engineering Description Design and development of medical device packaging or sterilization cases. Includes qualification/testing of packaging configurations and process ...

Merit Medical

Assembler

Sarasota, FL · On-site

$17.25 - $21.25/hr

At Merit Medical, our mission is to create innovative medical devices that improve lives. Our goal ... testing equipment required for periodic product and process testing. 9. Working overtime may be ...

MRINetwork Jobs

Medical Technologist

Avon Park, FL · On-site

Job Summary The Medical Laboratory Scientist II performs a wide range of diagnostic testing with ... Medical Device, Construction/Engineering, Government & Critical Infrastructure. Contracting ...

MRINetwork Jobs

Medical Technologist

Avon Park, FL · On-site

Job Summary The Medical Laboratory Scientist II performs a wide range of diagnostic testing with ... Medical Device, Construction/Engineering, Government & Critical Infrastructure. Contracting ...

MRINetwork Jobs

Medical Technologist

Avon Park, FL · On-site

Job Summary The Medical Laboratory Scientist II performs a wide range of diagnostic testing with ... Medical Device, Construction/Engineering, Government & Critical Infrastructure. Contracting ...

MRINetwork Jobs

Medical Technologist

Avon Park, FL · On-site

Job Summary The Medical Laboratory Scientist II performs a wide range of diagnostic testing with ... Medical Device, Construction/Engineering, Government & Critical Infrastructure. Contracting ...

atrion

Sr. Manager - Quality Assurance

Davie, FL

Continuous innovation and improvement of testing methods and processes are essential aspects of ... EU Medical Device Directive (93/42/EEC); Canadian Medical Devices Regulation (SOR98-282); Japanese ...

Stark Pharma Solutions Inc

Manufacturing Engineer

Orlando, FL · On-site

$68K - $87K/yr

... or medical device industry. This entry-level role is ideal for recent graduates or candidates with internship or co-op experience who are eager to build a career in regulated manufacturing. The ...

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Internship Medical Device Testing information

What types of projects and hands-on experiences can I expect during a medical device testing internship?

As a Medical Device Testing intern, you can expect to participate in a variety of projects that involve evaluating the safety, functionality, and reliability of medical devices. Typical responsibilities may include assisting with test setup, executing test protocols, recording and analyzing data, and collaborating with engineers and regulatory teams to ensure compliance with industry standards. Interns often gain exposure to specialized lab equipment, quality assurance practices, and regulatory documentation, all while working closely with experienced professionals in a team-oriented environment. This hands-on experience is valuable for building technical skills and understanding the product development lifecycle in the medical device industry.

What is the difference between Internship Medical Device Testing vs Medical Device Quality Assurance Intern?

AspectInternship Medical Device TestingMedical Device Quality Assurance Intern
Required CredentialsTypically enrolled in related health sciences or engineering programsSimilar educational background, often in quality management or engineering
Work EnvironmentLaboratory and testing facilities, hands-on testing activitiesQuality management departments, documentation, and compliance tasks
Employer & Industry UsageManufacturers, testing labs, R&D departmentsManufacturers, regulatory agencies, compliance teams
Search & Comparison IntentUnderstanding testing roles in medical device developmentExploring quality assurance internship opportunities in medical devices

Internship Medical Device Testing focuses on hands-on testing and validation of medical devices, while Medical Device Quality Assurance Interns concentrate on ensuring compliance, documentation, and quality standards. Both roles are essential in the medical device industry and often overlap in skills and environment, but they serve different aspects of product development and regulation.

What are the key skills and qualifications needed to thrive in a medical device testing internship?

To thrive in a Medical Device Testing internship, you need a solid background in biomedical engineering, life sciences, or a related field, often supported by coursework in device regulations and laboratory methods. Familiarity with testing equipment, data analysis software, and relevant standards like ISO 13485 or FDA regulations is typically expected. Strong attention to detail, effective communication, and problem-solving skills set standout candidates apart. These abilities ensure accurate testing, regulatory compliance, and clear reporting, which are critical for patient safety and product quality.

What is an internship in medical device testing?

An internship in medical device testing is a temporary position where students or recent graduates gain hands-on experience working with medical devices to ensure their safety, effectiveness, and compliance with regulatory standards. Interns typically assist in performing laboratory tests, documenting results, and supporting engineers or quality assurance teams. This role helps interns understand industry protocols, testing methodologies, and regulatory requirements while developing practical skills for a future career in medical technology.

What are the most commonly searched types of Medical Device Testing jobs in Florida?

The most popular types of Medical Device Testing jobs in Florida are:

Internship Medical Device Testing jobs near you

Clinical Engineer System Integration (HL7 Experience Required)

Nicklaus Children's Health System

Miami, FL • On-site

$159K/yr

Full-time

Re-posted 10 days ago

Job description

Description
Job Summary
Acts as technical subject matter expert on medical device connectivity and provides expert knowledge in developing and maintaining interfaces in a healthcare environment. Ensures effective and safe procurement, deployment, and sustainment of integrated medical devices/systems. Serves as a medical device/system subject matter expert to clinical staff, vendors, and the Clinical Engineering department. Supports, among others, the following integrated medical devices/systems: patient monitoring, nurse call, infusion pumps, vital signs, EEG, perfusion systems, OR video integration, cardiology ultrasounds, interactive patient systems, environmental monitoring systems, DICOM nodes, post-processing software, gastrointestinal systems, digital dental systems and review/acquisition software, HL7 brokers, Cerner EMR, and CMMS. Oversees multiple medical device/system projects with diverse stakeholders, timelines, and resources. Sustains medical device/system hardware, software, firmware, networking, servers, clients, databases, and interfaces with the support of clinical staff, in-house technical resources, and vendors. Sustainment scenarios include resolving end-user issues, supporting downtimes, requesting feature requests, performing vendor remediation, and responding to recalls or patient incident investigations.
Job Specific Duties
  • Serves as a medical device/system subject matter expert to clinical staff, vendors, and the Clinical Engineering department.
  • Responsible for the assessment, design, procurement, installation, monitoring, maintenance, troubleshooting, documentation, configuration, performance, and testing of medical device/system hardware, software, firmware, networking, servers, clients, databases, and interfaces with the support of clinical staff, in-house technical resources, and vendors.
  • Responsible for resolving end-user issues, supporting downtimes, requesting feature requests, performing vendor remediation, and responding to recalls or patient incident investigations.
  • Develops and maintains an up-to-date inventory and technical reference documentation of medical devices/systems and their interconnections for use in end-user issues, downtimes, feature requests, vendor remediation, recalls, repairs, upgrades, incident investigations, or capital planning.
  • Oversees and participates in multiple medical device/system projects with diverse stakeholders, timelines, and resources.
  • Monitors and adopts the industry's and health system's latest best practices for integrated medical devices/systems, specifically for risk assessments, IT change management, FDA or vendor hazard/recalls, or patient incident root cause analysis.
  • Juggles multiple medical device/system issues requiring adequate response, delegation, prioritization, or escalation.
  • Participates in a rotating on-call schedule to respond to medical device/system end-user issues and device/system downtimes in a 24/7/365 environment.
  • Provides functional and technical guidance to assigned personnel on a daily basis including scheduling, monitoring, reviewing of systems studies, project and program.

Qualifications
Minimum Job Requirements
  • Bachelor's Degree in Biomedical Engineering or related major (OR) 5+ years of equivalent relevant experience.
  • 4-7 years of hands-on experience in medical systems configuration and administration.
  • 4-7 years o f e xperience designing, implementing, and supporting clinical application systems.
  • 4-7 years of work experience with SQL Server relational database systems.
  • 4-7 years of work experience in HL7 interface engines.

Knowledge, Skills, and Abilities
  • Healthcare Technology Management and Information Technology relevant certifications strongly preferred.
  • Ability to communicate effectively both verbally and writing.
  • Strong working knowledge of healthcare technology management, project management, information technology, and process improvement.
  • Strong working knowledge of Windows OS, MAC OS, Linux OS, HL7 brokers, XML, JAVA, SQL, DICOM, and Cerner EMR.
  • Strong working knowledge of patient monitoring, nurse call, infusion pumps, vital signs, EEG, perfusion, OR/Cath Lab video integration, Cardiology device/systems, interactive patient systems, environmental monitoring systems, DICOM nodes, post processing software, gastrointestinal systems, dental systems, HL7 brokers, and CMMS.
  • Strong soft skills (communication, flexibility, leadership, teamwork, time management, creativity, ability to work under pressure, self-motivation, accountability, etc.)
  • Practical experience with project delivery and systems development.
  • Experience in leading hospital applications suites preferred.
  • Working knowledge of HL7 standards and custom interface products.
  • Strong understanding of enterprise Wide Area Network (WAN), Local Area Network (LAN), TCP/IP, Ethernet.

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