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Part Time Medical Device Jobs in Texas (NOW HIRING)

IQVIA

MedTech Part Time Clinical Consultant

Beaumont, TX · On-site

$60/hr

Ventricular medical device case support, including on call support. * Complete proactive rounds for patients receiving support and provide assistance. * Collaborate with the Clinical Support Center ...

IQVIA

MedTech Part Time Clinical Consultant

Lubbock, TX · On-site

$60/hr

Ventricular medical device case support, including on call support. * Complete proactive rounds for patients receiving support and provide assistance. * Collaborate with the Clinical Support Center ...

IQVIA

MedTech Part Time Clinical Consultant

Houston, TX · On-site

$60/hr

Ventricular medical device case support, including on call support. * Complete proactive rounds for patients receiving support and provide assistance. * Collaborate with the Clinical Support Center ...

IQVIA

Clinical Nurse Educator (per diem)

Dallas, TX · On-site

$40 - $45/hr

Utilize clinical nursing expertise to answer questions and address concerns with the medical device ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

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All JobsMedical Device JobsPart Time Medical Device JobsPart Time Medical Device Jobs in Texas

Part Time Medical Device information

See Texas salary details

$19

$46

$90

How much do part time medical device jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for part time medical device in Texas is $46.43, according to ZipRecruiter salary data. Most workers in this role earn between $32.69 and $55.53 per hour, depending on experience, location, and employer.

What is a part time medical device job?

Part-time medical device jobs involve working with medical equipment and technology, but on a reduced or flexible schedule rather than full-time hours. These roles can include sales, technical support, device training, field service, or clinical applications, and they are often available with medical device manufacturers or distributors. Part-time positions are ideal for professionals seeking work-life balance, students, or individuals looking to gain experience in the medical device industry without committing to a full-time role.

What skills and qualifications are needed to thrive as a part time medical device sales representative?

To thrive as a Part Time Medical Device Sales Representative, you need a background in life sciences, sales experience, and a solid understanding of medical device products and regulations. Familiarity with CRM systems, sales tracking tools, and sometimes certifications like Certified Medical Sales Professional (CMSP) are typically required. Strong interpersonal skills, persuasive communication, and resilience help build lasting relationships with healthcare professionals and drive sales. These skills and qualifications are crucial for effectively promoting products, meeting sales targets, and navigating the competitive healthcare market.

What are common challenges faced by part time medical device professionals, and how can they manage them?

Part-time medical device professionals often face challenges such as maintaining up-to-date product knowledge, adapting quickly to new regulatory changes, and building strong relationships with clients or clinical stakeholders despite limited hours. To manage these challenges, it's important to prioritize ongoing training, stay connected with team members via regular communication, and utilize digital resources for product updates. Leveraging flexible scheduling and setting clear expectations with managers can also help ensure effective collaboration and productivity within a part-time framework.

What is the difference between Part Time Medical Device vs Part Time Medical Equipment Technician?

AspectPart Time Medical DevicePart Time Medical Equipment Technician
CredentialsCertification in medical device management or related fieldsCertification in biomedical equipment technology or similar
Work EnvironmentHospitals, clinics, medical device companiesHospitals, repair shops, medical equipment suppliers
Industry UsageDesign, distribution, and management of medical devicesMaintenance, repair, and calibration of medical equipment
Search IntentPart Time Medical Device jobs and rolesPart Time Medical Equipment Technician roles

Part Time Medical Device roles typically focus on managing, distributing, or overseeing medical devices, often requiring knowledge of device regulations. In contrast, Part Time Medical Equipment Technicians primarily handle maintenance, repair, and calibration of medical equipment. Both roles are essential in healthcare settings but differ in responsibilities and skill sets.

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

The most popular types of Medical Device jobs in Texas are:

What cities in Texas are hiring for Part Time Medical Device jobs?

Cities in Texas with the most Part Time Medical Device job openings:

Part Time Medical Device jobs near you
Infographic showing various Part Time Medical Device job openings in Texas as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 14% Part Time, and 6% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $96,577 per year, or $46.4 per hour.

Medical Device Quality Remediation Consultants (Hybrid)

The FDA Group

Fort Worth, TX

Full-time, Part-time

Posted 16 days ago

Job description

Medical Device Quality Remediation Consultants

Location: North of Fort Worth, TX
Work Arrangement: Primarily Onsite / Hybrid Flexibility
Duration: Initial 3-month engagement with potential extension to 6+ months
Openings: 2 Consultants
Start: ASAP / Within the next few weeks
Schedule: Full-time preferred; qualified part-time consultants may also be considered

Position Overview

We are seeking two experienced Medical Device Quality Remediation Consultants to support a quality systems remediation initiative at a medical device organization in Texas.

The consultants will provide hands-on support addressing CAPA and complaint backlogs, FDA remediation activities, quality and regulatory records, and implementation of FDA Quality Management System Regulation (QMSR) requirements.

This engagement requires professionals who can move beyond high-level strategy and actively drive remediation activities through completion. The ideal consultants will be able to identify root causes, develop practical and sustainable corrective actions, and work collaboratively with site personnel to strengthen the overall Quality Management System.

Key Responsibilities

  • Drive investigation, remediation, and closure of open and aging CAPAs.
  • Address existing complaint-handling backlogs and support timely closure of complaint records.
  • Evaluate and improve complaint-handling processes to promote sustainable compliance.
  • Perform and/or support root-cause investigations and development of effective corrective actions.
  • Support remediation activities resulting from FDA inspection observations.
  • Assist with quality and regulatory record management and remediation.
  • Support implementation and integration of FDA QMSR requirements into the existing Quality Management System.
  • Ensure remediation activities align with applicable FDA requirements and ISO 13485.
  • Identify systemic quality issues and develop practical corrective actions that address underlying causes rather than short-term fixes.
  • Collaborate with Quality, Regulatory, Operations, and other cross-functional stakeholders to drive remediation activities to completion.

Required Qualifications

  • Significant medical device industry experience.
  • Strong working knowledge of ISO 13485.
  • Strong knowledge of 21 CFR Part 820 and FDA QMSR requirements.
  • Demonstrated hands-on experience with CAPA remediation and closure.
  • Strong complaint handling and complaint investigation experience.
  • Experience supporting remediation following FDA inspections and observations.
  • Experience with quality records and regulatory documentation.
  • Strong root-cause analysis, investigation, and problem-solving capabilities.
  • Ability to develop sustainable, compliant solutions and effectively drive them through implementation.
  • Comfortable working in a hands-on consulting environment with significant interaction with site personnel.

Work Arrangement

This engagement will require frequent onsite presence in Texas. Some administrative and documentation activities may be completed remotely when appropriate.

Local candidates are preferred; however, travel can be accommodated for highly qualified consultants who are not located in the area.

Ideal Candidate

The ideal consultant is a seasoned medical device Quality Systems/Remediation professional with substantial hands-on experience in CAPA, complaints, FDA remediation, ISO 13485, and FDA QMSR/21 CFR Part 820.