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Remote Medical Device Auditor Jobs in Oregon (NOW HIRING)

Research Fellow, Medical Device Toxicologist

OR · On-site +1

$150K - $200K/yr

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Research Fellow - Medical Device Toxicologist will provide cross functional Preclinical medical ... Remote All qualified applicants will receive consideration for employment without regard to race ...

Medical Device & Diagnostics - CRA 2 - US Remote

OR · On-site +1

$105/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

We are currently seeking Experienced Device CRA 2s to lead and support our Medical Device ... Varied hours may be required. #LI - Remote Applications will be accepted on an ongoing basis. Learn ...

Quality Assurance Specialist, Sr

Newberg, OR · Remote

$86K - $119K/yr

... Medical Device regulations and standards including US-FDA, Health Canada, and the European Union ... Manages the internal audit process, leading audit teams and acting as a lead internal auditor, for ...

Claims Auditor

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Pharmacy auditing, medical billing auditing, or pharmacy technician experience is strongly ... This position is remote, with occasional travel to the corporate office. Essential Job Duties

DRG Auditor (REMOTE)

OR · On-site +1

$27.25 - $31/hr

Position Summary The DRG Auditor is responsible for reviewing post-billed inpatient claims to ... Navigate medical records efficiently, targeting specific sections (e.g., discharge summary ...

Learning Experience Designer - Remote

OR · Remote

$66K - $90K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Salary Minimum: $66,000 Salary Maximum: $90,000 Arthrex, Inc. is a global medical device company ... This position is a remote opportunity. Duties and Responsibilities: * Design and develop engaging ...

Coding Compliance Auditor

OR · Remote

$75K - $90K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... remote-first, high-growth environment. * Review medical records and clinical documentation to ... Prior coding or auditing experience in a Medicaid environment. * Experience providing individual ...

Clinical Review QC Auditor

$68K - $104K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Diagnostic Related Groups (DRG) Clinical Auditor will be responsible for performing DRG ... This is a remote position. ESSENTIAL FUNCTIONS & RESPONSIBILITIES: * Review medical records to ...

Clinical Review QC Auditor

$68K - $104K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Diagnostic Related Groups (DRG) Clinical Auditor will be responsible for performing DRG ... This is a remote position. ESSENTIAL FUNCTIONS & RESPONSIBILITIES: * Review medical records to ...

Senior Software Engineer- Android (REMOTE)

OR · Remote

$89K - $170K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... medical device innovation. The ideal candidate is passionate about software development, thrives in a collaborative environment, and is motivated to deliver reliable, scalable solutions that drive ...

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Showing results 1-20

Remote Medical Device Auditor information

What are common challenges faced by remote medical device auditors, and how can they be managed?

Remote Medical Device Auditors often face challenges such as ensuring thorough compliance assessments without on-site access and effectively communicating with diverse client teams across different time zones. To manage these challenges, auditors leverage robust virtual collaboration tools, detailed documentation, and clear communication protocols. Staying up to date with evolving regulatory standards and maintaining strong organizational skills are also critical for success in this role. Proactive planning and flexibility help auditors adapt to varied client needs and maintain audit quality remotely.

What skills and qualifications are needed to thrive as a remote medical device auditor?

To thrive as a Remote Medical Device Auditor, you need a solid understanding of medical device regulations (such as ISO 13485, FDA 21 CFR Part 820), quality management systems, and relevant industry experience, often supported by a degree in science, engineering, or a related field. Familiarity with auditing software, remote communication tools, and recognized auditor certifications (like IRCA or ASQ) is typically required. Strong attention to detail, analytical thinking, and effective communication are essential soft skills for evaluating compliance and collaborating with client teams remotely. These competencies ensure thorough, accurate audits and help organizations maintain regulatory compliance and uphold product safety standards.

What is a remote medical device auditor?

Remote Medical Device Auditors are professionals who evaluate medical device manufacturers' compliance with regulatory standards and quality systems, such as ISO 13485, without being physically present at the site. They conduct audits using digital tools, video conferencing, and document reviews to ensure products meet safety and quality requirements. This role requires strong knowledge of medical device regulations and excellent communication skills to work effectively with clients and regulatory bodies from a distance.

What are popular job titles related to Remote Medical Device Auditor jobs in Oregon?

For Remote Medical Device Auditor jobs in Oregon, the most frequently searched job titles are:

What cities in Oregon are hiring for Remote Medical Device Auditor jobs?

Cities in Oregon with the most Remote Medical Device Auditor job openings:

Infographic showing various Remote Medical Device Auditor job openings in Oregon as of August 2026, with employment types broken down into 88% Full Time, 8% Part Time, and 4% Contract. Highlights an 100% Remote job distribution.

Research Fellow, Medical Device Toxicologist

Bausch + Lomb

OR • On-site, Remote

$150K - $200K/yr

Full-time

Dental, Vision, Life, Retirement, PTO

This job post has expired 1 day ago. Applications are no longer accepted.


Bausch & Lomb rating

8.6

Company rating: 8.6 out of 10

Based on 39 frontline employees who took The Breakroom Quiz

22nd of 540 rated manufacturers


Job description

Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the world-from the moment of birth through every phase of life. Our mission is simple, yet powerful: helping you see better, to live better.
Our comprehensive portfolio of over 400 products is fully integrated and built to serve our customers across the full spectrum of their eye health needs throughout their lives. Our iconic brand is built on the deep trust and loyalty of our customers established over our 170-year history. We have a significant global research, development, manufacturing and commercial footprint of approximately 13,000 employees and a presence in approximately 100 countries, extending our reach to billions of potential customers across the globe. We have long been associated with many of the most significant advances in eye health, and we believe we are well positioned to continue leading the advancement of eye health in the future.
The Research Fellow - Medical Device Toxicologist will provide cross functional Preclinical medical device expertise supporting internal and external stakeholders pertaining to biocompatibility and associated focus areas, for medical device development, product expansion and maintenance. The Research Fellow - Medical Device Toxicologist is responsible for professional, first-line impression of the department within and outside the company through effective interactions via written and oral communications.
Responsibilities:
  • Manage team responsible for medical device biocompatibility support
  • Responsible for project strategies, risk assessments, biocompatibility evaluation plans and reports for medical devices
  • Ensures that development and execution of nonclinical strategies are aligned with product development and life cycle management activities, and with key regulatory expectations and milestones
  • Ensures that essential nonclinical data are obtained, and effectively presented for successful clinical development, regulatory and quality compliance, market launch, and maintenance of business
  • Coaches and mentors junior staff
  • Deep understanding of medical device relevant standards staying abreast of changes to applicable industry practice and guidance documents
  • Implement new and revised standards into product development projects and/or assess impact on existing products as appropriate
  • Authors and reviews department's technical documents as needed
  • Manage interactions with other functions (e.g., Product Development, Clinical Development, Analytical Chemistry, Regulatory, Quality, Compliance)
  • Liaise with company international offices on nonclinical safety matters for country-specific submissions/registrations and maintenance of business activities
  • Development and maintenance of department best practices and processes

Requirements:
  • Ph.D. in Toxicology or related discipline
  • 12+ years of relevant Medical Device industry experience
  • Experience managing a team
  • DABT preferred
  • Ophthalmic medical device experience a plus

This position may be available in the following location(s): Remote
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.
For U.S. locations that require disclosure of compensation, the starting pay for this role is between $150,000.00 and $200,000.00. The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors.
U.S. based employees may be eligible for short-term and/or long-term incentives. They may also be eligible to participate in medical, dental, vision insurance, disability and life insurance, a 401(k) plan and company match, a tuition reimbursement program (select degrees), company holidays, and well-being benefits, among others. U.S. based employees are also eligible to receive sick time, floating holidays and paid vacation.
Job Applicants should be aware of job offer scams perpetrated through the use of the Internet and social media platforms.
To learn more please read Bausch + Lomb's Job Offer Fraud Statement.
Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.

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About Bausch & Lomb

Sourced by ZipRecruiter

Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the world--from the moment of birth through every phase of life. Our mission is simple, yet powerful: helping you see better, to live better. Our comprehensive portfolio of over 400 products is fully integrated and built to serve our customers across the full spectrum of their eye health needs throughout their lives. Our iconic brand is built on the deep trust and loyalty of our customers established over our nearly 170-year history. We have a significant global research, development, manufacturing and commercial footprint of approximately 12,500 employees and a presence in approximately 100 countries, extending our reach to billions of potential customers across the globe. We have long been associated with many of the most significant advances in eye health, and we believe we are well positioned to continue leading the advancement of eye health in the future.

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Bridgewater, NJ, US

Year founded

1853