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Mdr Jobs in Tennessee (NOW HIRING)

Bioventus

Sr Quality Engineer

Memphis, TN · On-site

$86K - $116K/yr

Ensure medical device regulatory requirements (21 CFR 820, EU MDD/MDR, ISO 13485:2016 and IEC 60601 series) related to design control and process/product goals (e.g., process capability, yield ...

CONMED

Design Quality Engineer II

Memphis, TN · On-site

The Design Quality Engineer serves as the key resource for ensuring compliance to ISO, EU MDR, and FDA QSR requirements for Medical Devices. The Design Quality Engineer takes the lead with quality ...

STERIS Corporation

Quality Specialist

Chattanooga, TN · On-site

... EU MDR and other applicable regulatory standards. This role coordinates document control transactions, site record retention, calibration and inspection activities. In addition, the Quality ...

US Endoscopy

Quality Specialist

Chattanooga, TN · On-site

... EU MDR and other applicable regulatory standards. This role coordinates document control transactions, site record retention, calibration and inspection activities. In addition, the Quality ...

US Endoscopy

Quality Specialist

Chattanooga, TN · On-site

... EU MDR and other applicable regulatory standards. This role coordinates document control transactions, site record retention, calibration and inspection activities. In addition, the Quality ...

Steris Corporation

Quality Specialist

Chattanooga, TN · On-site

... EU MDR and other applicable regulatory standards. This role coordinates document control transactions, site record retention, calibration and inspection activities. In addition, the Quality ...

Vivos Holdings, LLC

SR CYBERSECURITY ENGINEER

Smyrna, TN · On-site

$120 - $180/hr

Own and administer security platforms including SIEM/MDR/XDR, Endpoint Detection & Response (EDR), and Identity & Access Management (MFA, PIM/PAM).* Lead threat detection, alert tuning, threat ...

Vivos Holdings

SR CYBERSECURITY ENGINEER

Smyrna, TN · On-site

$110 - $150/hr

Own and administer security platforms including SIEM/MDR/XDR, Endpoint Detection & Response (EDR), and Identity & Access Management (MFA, PIM/PAM).Lead threat detection, alert tuning, threat hunting ...

Vivos Holdings

SR CYBERSECURITY ENGINEER

Smyrna, TN · On-site

Own and administer security platforms including SIEM/MDR/XDR, Endpoint Detection & Response (EDR), and Identity & Access Management (MFA, PIM/PAM). * Lead threat detection, alert tuning, threat ...

SwiftCruit

IT Security Administrator

Memphis, TN · On-site

$70 - $110/hr

MDR (Managed Detection & Response) * Email Security Gateways * Backupand Disaster Recovery Solutions * Performing incident response * Monitoring networks and systems Preferred experience: * Managing ...

VIVOS HOLDINGS

SR CYBERSECURITY ENGINEER

Smyrna, TN · On-site +1

Own and administer security platforms including SIEM/MDR/XDR, Endpoint Detection & Response (EDR), and Identity & Access Management (MFA, PIM/PAM). * Lead threat detection, alert tuning, threat ...

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Mdr information

See Tennessee salary details

$16

$42

$63

How much do mdr jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for mdr in Tennessee is $42.83, according to ZipRecruiter salary data. Most workers in this role earn between $35.14 and $51.25 per hour, depending on experience, location, and employer.

What is an MDR?

An MDR (Market Development Representative) is a sales professional responsible for identifying and qualifying potential leads for a company's products or services. They focus on early-stage prospecting, researching target markets, and engaging with potential customers to generate sales opportunities. MDRs work closely with sales and marketing teams to ensure a seamless handoff of qualified leads for further nurturing and closing. Their role is crucial in driving business growth by expanding the company's customer base.

What does a typical day look like for a Medical Device Reprocessing (MDR) technician?

A typical day for an MDR Technician involves cleaning, disinfecting, and sterilizing surgical instruments and medical devices according to strict protocols. You'll routinely inspect equipment, assemble instrument trays, document processes, and ensure all items meet quality assurance standards. MDR Technicians frequently collaborate with surgical teams and other healthcare professionals to meet tight turnaround times for critical instruments. This is a hands-on role that requires adaptability, precision, and a commitment to patient safety, often performed in hospital central sterile departments or specialized clinics.

What are the key skills and qualifications needed to thrive in the MDR position, and why are they important?

To thrive as a Medical Device Reprocessing (MDR) Technician, you need knowledge of sterilization processes, infection control standards, and a high school diploma or equivalent, often supplemented with formal MDR certification. Familiarity with autoclaves, washer-disinfectors, and tracking systems is necessary for proper equipment handling. Attention to detail, teamwork, and effective communication are important soft skills in this role. These abilities ensure patient safety and efficient support of clinical procedures in healthcare environments.

What are popular job titles related to Mdr jobs in Tennessee?

For Mdr jobs in Tennessee, the most frequently searched job titles are:

What job categories do people searching Mdr jobs in Tennessee look for?

The top searched job categories for Mdr jobs in Tennessee are:

What cities in Tennessee are hiring for Mdr jobs?

Cities in Tennessee with the most Mdr job openings:

Mdr jobs near you
Infographic showing various Mdr job openings in Tennessee as of August 2026, with employment types broken down into 95% Full Time, 1% Part Time, and 4% Contract. Highlights an 77% Physical, 7% Hybrid, and 16% Remote job distribution, with an average salary of $89,078 per year, or $42.8 per hour.

Sr Quality Engineer

Bioventus

Memphis, TN • On-site

$86K - $116K/yr

Full-time

Posted 24 days ago

Job description

Are you ready to work for a more active world?
At Bioventus, our business depends on developing our people. We invest in you and challenge you to be the best. We value our colleagues for their different perspectives and individual contributions, and our leaders listen. Our success rests on working together to achieve shared goals and rewards. Join a diverse team of global colleagues driven to help patients resume and enjoy active lives.
The Sr Quality Engineer provides quality engineering expertise to manufacturing, engineering, quality control/assurance and process/product development teams to ensure our products are designed and manufactured to a high level of quality, and compliant with medical device regulations.What you'll be doing
  • Ensure medical device regulatory requirements (21 CFR 820, EU MDD/MDR, ISO 13485:2016 and IEC 60601 series) related to design control and process/product goals (e.g., process capability, yield, reliability) are met utilizing project planning and execution skills.
  • Identify and manage needs/requirements and assist with the creation and/or modification of product and process specifications
  • Lead design transfer activities focused in development of gage design, inspection processes, GR&R, capability studies and process validation
  • Actively participate in Design Review activities of new products and work closely with product design teams to manage quality considerations during all PLM stages of product development
  • Provide guidance and work to solve significant or chronic process or product problems. Discuss customer concerns or complaints with Marketing and Sales as needed
  • Generate, analyze, and present reports on quality related Key Performance Indicators (KPIs) such as line yields, final release, supplier performance and customer experiences to internal product improvement teams
  • Support Quality Systems such as delivery holds, internal and external audits, CAPA and investigations
  • Update and revise procedures to consistently meet regulatory requirements such as EU MDR, IEC 60601 series, ISO 13485:2016, 21 CFR 820, etc.
  • Analyze and act on process trend data including leading investigations, root cause analysis and assist with corrective actions.
  • Hold oneself and others accountable to conduct business in a manner compliant with Bioventus' Code of Compliance and Ethics, policies and procedures and internal controls applicable to their role.
  • Other duties as assigned

What you'll bring to the table
  • Bachelor's degree (Masters preferred), in an Engineering discipline or equivalent technical background, with emphasis or experience in electronics, circuits and/or software. Electrical Engineering or related fields preferred.
  • Minimum 5 years (with Bachelor's) or 4 years (with Master's) of experience within the medical device industry with a comprehensive understanding of, and ability to interpret regulations and guidelines governing medical devices including ISO 13485 and 21 CFR 820 and EU MDD/MDR.
  • Strong working knowledge of process and product development and validation methodologies (IQ,OQ,PQ).
  • Experience interacting directly with suppliers, Manufacturing, and Manufacturing support organizations.
  • Understanding and experience in applying quality engineering concepts such as process capability analysis, risk management, PFMEA and DFMEA.
  • Previous Quality Engineering or Product Development experience and GD&T and electronics knowledge/experience is required.

Are you the top talent we are looking for?
Apply now! Hit the "Apply" button to send us your resume and cover letter.
Bioventus is committed to fostering an inclusive and diverse community of employees with a strong sense of belonging. We believe we are bettered by all forms of diversity and take pride in working with top talent from every walk of life. In the spirit of inclusivity, qualified applicants will be considered without regard to age, ethnicity, disability, gender, veteran status, gender expression, gender identity, nationality, race, religion or sexual orientation. All individuals, regardless of personal characteristics, are encouraged to apply.

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