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Medical Device Regulatory Auditor Jobs (NOW HIRING)

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Senior Regulatory Affairs Specialist - Medical Devices

Alameda, CA · On-site

$50 - $65/hr

S. medical device submissions . This individual will serve as a regulatory subject matter expert and partner closely with cross-functional teams to support new product approvals, maintain regulatory ...

BSI Group

Be given training in ISO 13485 Lead Auditor training, MDSAP (Medical Device Single Audit Programme) and MDR (Medical Device Regulation) * Initially observe how audits are conducted but then grow to ...

BSI Prof Serv EHS West

Be given training in ISO 13485 Lead Auditor training, MDSAP (Medical Device Single Audit Programme) and MDR (Medical Device Regulation) * Initially observe how audits are conducted but then grow to ...

Apple

Senior Lead Auditor (Medical Devices)

Cupertino, CA · On-site

$99K - $122K/yr

... medical device regulatory requirements (e.g. ISO 13485, MDSAP requirements, China GMP, EU MDR ... auditor certification or internal auditor certification Attention to detail, well organized and ...

CEDENT

Regulatory Affairs Specialist

Bedford, MA · On-site

... auditor questions and requests. * Keep abreast of new or changed regulations and standards and ... Experience in regulatory submissions to medical device regulatory bodies a plus; e.g., FDA, Health ...

BSI Group

Medical Device QMS Auditor

Concord, NC · Remote

$98K - $123K/yr

Job Title: Medical Device QMS Auditor Location: Candidates must reside in one of the following ... Our Medical Devices (or Regulatory Services) team ensures patient safety while supporting timely ...

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Medical Device Regulatory Auditor information

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How much do medical device regulatory auditor jobs pay per hour?

As of Sep 12, 2026, the average hourly pay for medical device regulatory auditor in the United States is $39.57, according to ZipRecruiter salary data. Most workers in this role earn between $31.73 and $46.88 per hour, depending on experience, location, and employer.

What are popular job titles related to Medical Device Regulatory Auditor jobs?

For Medical Device Regulatory Auditor jobs, the most frequently searched job titles are:

Contract Medical Device Lead Auditor

Schaumburg, IL • On-site

DQS
See more jobs at DQSexternal

Part-time

Re-posted 29 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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