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Part Time Medical Device Auditor information

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

As of Sep 2, 2026, the average hourly pay for part time medical device auditor in the United States is $21.62, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $27.40 per hour, depending on experience, location, and employer.

What does a part time medical device auditor do?

A Part Time Medical Device Auditor is responsible for assessing and evaluating medical device manufacturers to ensure they comply with regulatory standards and quality management systems, such as ISO 13485. Their duties include reviewing documentation, conducting on-site or remote audits, and preparing detailed reports on findings. Working part-time, they may focus on specific audits or clients, providing flexibility while ensuring that safety and compliance standards are met within the medical device industry.

What are the key skills and qualifications needed to thrive as a part time medical device auditor?

To excel as a Part Time Medical Device Auditor, you need in-depth knowledge of medical device regulations, quality management systems (such as ISO 13485), and relevant auditing practices, often supported by a degree in a life science or engineering field. Familiarity with audit management software, regulatory databases, and recognized certifications like IRCA or RABQSA are commonly required. Strong analytical thinking, attention to detail, and effective communication are crucial soft skills for assessing compliance and presenting findings. These competencies ensure audits are thorough, regulatory standards are met, and patient safety and product quality are maintained.

What are some typical challenges faced by part time medical device auditors, and how can they be managed effectively?

Part-time medical device auditors often face the challenge of balancing multiple assignments across different organizations while staying up-to-date with evolving regulatory standards. Time management and strong organizational skills are essential, as audits must be conducted thoroughly within limited hours. Additionally, auditors must quickly adapt to varied company processes and documentation practices. Effective communication with client teams and ongoing professional development help ensure compliance and consistent audit quality, even when working part-time.

What is the difference between Part Time Medical Device Auditor vs Part Time Medical Device Quality Inspector?

AspectPart Time Medical Device AuditorPart Time Medical Device Quality Inspector
CertificationsISO 13485 Auditor, CQEQC Certifications, GMP training
Work EnvironmentAuditing facilities, reviewing documentationInspecting products, testing samples
Employer & Industry UsageMedical device companies, certification bodiesManufacturers, quality control departments

While both roles focus on quality, the Part Time Medical Device Auditor primarily conducts audits to ensure compliance with standards, whereas the Part Time Medical Device Quality Inspector performs hands-on inspections of products. Auditors review processes and documentation, while inspectors examine physical items. Both roles are essential in maintaining medical device safety and quality, but they differ in scope and daily tasks.

What cities are hiring for Part Time Medical Device Auditor jobs?

Cities with the most Part Time Medical Device Auditor job openings:

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

The most popular types of Medical Device Auditor jobs are:

What states have the most Part Time Medical Device Auditor jobs?

States with the most job openings for Part Time Medical Device Auditor jobs include:

Part Time Medical Device Auditor jobs near you
Infographic showing various Part Time Medical Device Auditor job openings in the United States as of July 2026, with employment types broken down into 83% Full Time, 14% Part Time, 2% Contract, and 1% Nights. Highlights an 86% Physical, 4% Hybrid, and 10% Remote job distribution, with an average salary of $44,967 per year, or $21.6 per hour.

Contract Medical Device Lead Auditor

DQS

Schaumburg, IL • On-site

Part-time

Re-posted 18 days ago

Job description

Your role

Medical Device Lead Auditor
DQS Inc. has an immediate contract opportunity for a Medical Device Lead Auditor. Working closely with your schedulers, you will visit client locations and perform the audits as specified. Position is home based with extensive travel.
Job Responsibility:
  • Knowledge of principles and methods for management systems audits.
  • Experience with internal, 2nd or 3rd party ISO-9001, ISO 13485, and/ or GMP auditing.
  • Preference given to RAB-QSA or Exemplar Global Lead Auditor or Auditor qualification.
  • Ability to develop an audit scope and audit plan and manage audit team activities.
  • Ability to present the audit team conclusions to the customer and review customer resolution of any nonconformities.
  • Must be able to assess customer needs and meet UL DQS service and customer satisfaction standards.
  • Work independently and project a professional image appropriate to the work environment.
  • Extensive travel.

Your profile

  • Bachelor's degree in a physical or life science or electrical, mechanical or biotechnology engineering required
  • Minimum of four years experience in quality systems management.
  • Minimum of four years experience in medical device development, manufacture and/or testing, with demonstrated knowledge of US, Canada and EU medical device regulatory requirements, experience with device submittals and knowledge of risk management principles such as ISO 14971.
  • Passed or ability to pass an accredited 40-hour ISO 9001 or ISO 13485 lead auditor course.
  • Experience in implementation of ISO 13485, MDD and/ or CMDCAS desired.
EEO is the Law
Right to Work Poster (English)
DQS Inc. is an Equal Opportunity Employer. Minorities/Women/Veterans/Disabled

EQUAL EMPLOYMENT OPPORTUNITY (EEO)

Qualified applicants are considered for employment without regard to race, religion, sex, national origin, age, marital status, sexual orientation, veteran status, disability, or other protected characteristic.

The employer is subject to certain governmental recordkeeping and reporting requirements for the administration of civil rights laws and regulations. In order to comply with these laws, the employer invites employees to voluntarily self-identify their race or ethnicity. Submission of this information is voluntary and refusal to provide it will not subject you to any adverse treatment. The information obtained will be kept confidential and may only be used in accordance with the provisions of applicable laws, executive orders, and regulations, including those that require the information to be summarized and reported to the federal government for civil rights enforcement. When reported, data will not identify any specific individual.

Right to Work Poster (English)

EEO is the Law

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