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Medical Device Support Jobs in Tennessee (NOW HIRING)

Revance

Regulatory Device Specialist

Johnson City, TN · On-site

$65K - $73K/yr

They will also support the preparation, review and archival of electronic and paper regulatory ... Preferred Experience: * Minimum of 3 years Medical Device Regulatory Experience required ...

Revance

Regulatory Device Specialist

Johnson City, TN · Remote

$65K - $73K/yr

They will also support the preparation, review and archival of electronic and paper regulatory ... Preferred Experience: * Minimum of 3 years Medical Device Regulatory Experience required ...

IQVIA

Inside Sales Representative

Nashville, TN · On-site

$30 - $33/hr

With a focus on providing talent for field/inside sales, medical device support, clinical support, and medical affairs our CSMS division has 10,000+ field professionals in more than 30 countries ...

IQVIA

Inside Sales Representative

Memphis, TN · On-site

$30 - $33/hr

With a focus on providing talent for field/inside sales, medical device support, clinical support, and medical affairs our CSMS division has 10,000+ field professionals in more than 30 countries ...

IQVIA

Work from Home

Memphis, TN · Remote

$18/hr

With a focus on providing talent for patient support, field/inside sales, medical device support, clinical support, and medical affairs our CSMS division has 10,000+ field professionals in more than ...

RXinsider LTD.

AVP Strategic Sourcing

Nashville, TN · On-site

$180 - $240/hr

The goals of SurgIntel analytics, medical device consulting, and physician engagement are to ... Promote strong client relationship management to improve client satisfaction and support ...

DSI

Retail Support Specialist

Nashville, TN

$26/hr

Resolve inquiries related to billing, account updates, plan changes, device support, and service ... Medical, Dental, Vision, and Life insurance are available on the first day of the month following ...

DSI

Retail Support Specialist

Nashville, TN · On-site

$26/hr

Resolve inquiries related to billing, account updates, plan changes, device support, and service ... Medical, Dental, Vision, and Life insurance are available on the first day of the month following ...

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Medical Device Support information

What is a medical device support specialist?

A Medical Device Support specialist is a professional who assists healthcare providers and patients with the installation, operation, troubleshooting, and maintenance of medical devices. They provide technical support, answer user questions, and help resolve issues related to device functionality and safety. Their role is essential in ensuring that medical equipment is used correctly and efficiently, contributing to better patient care and safety. They may also provide training and documentation to users, and sometimes liaise with manufacturers for more complex technical issues.

What are the key skills and qualifications needed to thrive as a medical device support specialist?

To thrive as a Medical Device Support specialist, you need a solid understanding of biomedical equipment, troubleshooting techniques, and an educational background in engineering or healthcare technology. Familiarity with device-specific software, diagnostic tools, and industry certifications like CBET (Certified Biomedical Equipment Technician) is often required. Strong problem-solving abilities, communication skills, and customer service orientation help professionals excel in assisting users and collaborating with healthcare teams. These skills ensure devices operate safely and efficiently, directly impacting patient outcomes and healthcare facility performance.

What are some typical challenges faced in a medical device support role, and how can they be addressed?

Medical Device Support professionals often encounter challenges such as troubleshooting complex technical issues, ensuring compliance with regulatory standards, and effectively communicating with both clinical staff and patients. Staying current with rapidly evolving device technologies and documentation requirements can also be demanding. These challenges can be addressed through continuous training, proactive communication, and close collaboration with engineering, quality assurance, and healthcare teams to resolve issues efficiently and maintain high standards of patient safety.

What are popular job titles related to Medical Device Support jobs in Tennessee?

For Medical Device Support jobs in Tennessee, the most frequently searched job titles are:

What job categories do people searching Medical Device Support jobs in Tennessee look for?

The top searched job categories for Medical Device Support jobs in Tennessee are:

What cities in Tennessee are hiring for Medical Device Support jobs?

Cities in Tennessee with the most Medical Device Support job openings:

Medical Device Support jobs near you
Infographic showing various Medical Device Support job openings in Tennessee as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 18% Part Time, and 4% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution.

Regulatory Device Specialist

Revance

Johnson City, TN • On-site

$65K - $73K/yr

Full-time

Medical, Life, Retirement, PTO

Posted 20 days ago

Key responsibilities

  • Prepare and submit regulatory documentation to FDA and other international regulatory agencies.

  • Review, interpret, and communicate regulations and guidance documents to ensure product submission compliance.

  • Support the management of international product registrations, license renewals, and amendments.

Job description

Position Summary:
The Regulatory Device Specialist prepares and submits high quality routine regulatory submissions to the FDA within company timelines and in accordance with regulatory guidelines and applicable federal laws. They will also support the preparation, review and archival of electronic and paper regulatory submissions ensuring compliance with FDA and other Health Authorities, company policies and procedures under the guidance of regulatory management.
This position serves as a subject matter expert on various domestic and foreign regulations for medical devices.
  • Reports to: Regulatory Affairs Manager
  • Location: Remote with occasional travel
  • Salary: *$65,000-$73,000 annually + annual performance bonus

*The final salary offered will depend upon factors that may include but are not limited to the quality and length of experience, education, and geographic location.
Essential Roles and Responsibilities:
  • Prepare pre-market submission reports / technical files per the requirements of key regulatory agencies (e.g. FDA, Health Canada, EU, APAC, Middle East).
  • Reviews, interprets, and communicates FDA/international regulations and guidance documents to ensure complete and scientifically sound product submissions.
  • Regulatory review of post-market product changes and decision on appropriate mechanism for change control (e.g. internal documentation, notification of change, supplemental submission).
  • Assist in the update, enhancement, and creation of internal policies and procedures.
  • Supports regulatory compliance to QSR, ISO, FDA, and other worldwide regulatory requirements as appropriate through customer complaints, internal audits and training systems.
  • Compile, submit, and manage international product registrations, license renewals, and registration amendments, including FDA 510(k)s, Health Canada Medical Device Licences, EU MDR Technical Documentation, UKCA, TGA (Australia), PMDA (Japan), ANVISA (Brazil), NMPA (China), MFDS (South Korea), COFEPRIS (Mexico), SFDA (Saudi Arabia), and MOHAP (UAE).
  • Prepare and manage export and country-specific documentation, including Certificates to Foreign Government (CFG), Certificates of Free Sale, Declarations of Conformity, ISO 13485/MDSAP certificates, and Letters of Authorization, and coordinate notarization, apostille, legalization, and consularization as required.
  • Assess new market opportunities by determining device classification, registration pathway, submission content, expected timelines, and in-country representation requirements; provide registration strategy input to new product launch and market entry plans.
  • Review labeling, Instructions for Use, and promotional materials for country-specific content, symbols, translation, and UDI requirements, and support product data submissions to GUDID, EUDAMED, and other national registries.
  • Support Notified Body, MDSAP, and international regulatory inspections and audits, including preparation of requested documentation and follow-up on findings and nonconformities.
  • Monitor and interpret evolving global regulations and guidance (e.g., EU MDR, UKCA transition, IMDRF harmonization initiatives), assess business impact, and communicate required actions to cross-functional stakeholders.
  • Perform other duties as assigned.

Preferred Experience:
  • Minimum of 3 years Medical Device Regulatory Experience required; aesthetics experience preferred
  • Solid understanding of cGMP for Medical Devices, ISO 13485, FDA and EU MDR requirements
  • Demonstrated experience obtaining and maintaining medical device registrations in at least three major markets outside the United States (e.g., EU, UK, Canada, Australia, Japan, China, Brazil, LATAM, Middle East, or APAC).
  • Hands-on experience authoring or compiling regulatory dossiers in multiple formats, including FDA 510(k), EU MDR 2017/745 Technical Documentation, IMDRF/STED Table of Contents, and ASEAN CSDT submissions.
  • Working knowledge of MDSAP, UKCA, and Notified Body review processes, and of country-specific labeling, translation, and UDI/registry requirements.
  • Ability to manage multiple concurrent international submissions across time zones

Preferred Education:
  • Bachelor's degree from a four year college or university.

Company Summary:
Revance is a global company developing, producing, and distributing industry-leading, differentiated products across aesthetics, skincare, and therapeutics. Revance drives innovation beyond convention to offer treatment options for individuals across generations. The Company's vision is to redefine excellence in aesthetics, skincare, and therapeutics through science-powered innovation, with an unwavering commitment to its providers, patients, and consumers. Revance's award-winning products are the result of robust research and development, a cornerstone for the Company, driven by renowned scientists. For more information about Revance, please visit us at www.revance.com.
What Revance invests in you:
  • Competitive Compensation including base salary and annual performance bonus.
  • Flexible PTO, holidays, and parental leave.
  • Generous healthcare benefits, HSA match, 401k match, employer paid life and disability insurance, pet insurance, wellness discounts and much more!

This section of the job description is required by the American with Disability Act (ADA). The ADA requires that job descriptions reflect the physical and mental demands required to effectively perform the essential duties of the job. The ADA prohibits employers from discriminating against a "qualified individual with a disability" in all aspects of the employment relationship. A "qualified individual with a disability" is "an individual who meets the education, experience, skill, and other job-related requirements of a position held or desired, and who, with reasonable accommodation, can perform the essential functions of a specified job."
Revance is an Equal Opportunity employer. All qualified applicants will receive consideration for employment based on merit, without regard to race, color, religion, sex, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law.

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