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Remote Contract Medical Device Jobs in Oregon (NOW HIRING)

Senior Staff Medical Writer (Remote)

Portland, OR ยท On-site +1

$143K - $238K/yr

Remote Stryker is hiring a Senior Staff Medical Writer to join our Endoscopy Division, to be based ... Expert knowledge of MEDDEV 2.7/1 Rev. 4, European Union Medical Device Regulation (EU MDR 2017/745 ...

New

Enterprise Account Executive

OR ยท On-site +1

$240K - $300K/yr

You have 5+ years of experience selling Enterprise SaaS or Medical Device products * You should ... Remote work : AcuityMD is committed to supporting full-remote flexibility for employees in the US.

You have 5+ years of experience selling Enterprise SaaS or Medical Device products * You should ... Remote work : AcuityMD is committed to supporting full-remote flexibility for employees in the US.

Work from Home

Portland, OR ยท Remote

$18/hr

Our teams help biopharma, medical device and diagnostic companies get their therapies to the people ... are looking for a 100% remote (work from home-WFH) contract Pharmacy Support Call Center ...

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Remote Contract Medical Device information

What is a remote contract medical device professional?

A Remote Contract Medical Device professional is an individual who works with medical device companies on a contract basis, often providing specialized services such as regulatory affairs, quality assurance, clinical research, or engineering support, all performed remotely. These professionals typically help organizations ensure that their medical devices meet regulatory standards, are safe for patients, and are effectively brought to market. Working remotely allows them to collaborate with clients globally without being physically present. Contract work means they are not permanent employees but are hired for specific projects or periods.

What are the key skills and qualifications needed to thrive as a remote contract medical device professional?

To thrive as a Remote Contract Medical Device Specialist, you need a comprehensive understanding of medical device regulations, product knowledge, and a relevant degree such as in biomedical engineering or life sciences. Familiarity with regulatory submission systems, quality management software, and certifications like ISO 13485 or RAC are often required. Excellent communication, self-motivation, and problem-solving skills help you manage projects independently and liaise with clients or regulatory bodies. These competencies are crucial to ensure compliance, maintain product quality, and effectively support clients in a remote work environment.

How do remote contract medical device professionals typically collaborate with on-site teams and ensure compliance with regulatory standards?

Remote contract medical device professionals frequently use digital communication tools to collaborate closely with on-site engineering, quality assurance, and regulatory teams. Regular video meetings, shared project management platforms, and clear documentation protocols help ensure that all parties stay aligned on project goals and compliance requirements. Remote professionals must be proactive in staying updated on evolving regulations and participate in virtual audits or reviews as needed. Building strong relationships with on-site contacts and maintaining prompt communication are key to overcoming challenges associated with remote work in this highly regulated industry.

What is the difference between Remote Contract Medical Device vs Remote Contract Medical Device Quality Assurance Specialist?

AspectRemote Contract Medical DeviceRemote Contract Medical Device Quality Assurance Specialist
CredentialsTypically requires engineering, regulatory, or technical certificationsRequires certifications in quality management systems (e.g., ISO 13485, FDA QSR)
Work EnvironmentPrimarily remote, collaborating with cross-functional teamsPrimarily remote, focusing on compliance, audits, and documentation
Employer & Industry UsageUsed across medical device companies for product development and supportUsed within quality departments to ensure regulatory compliance
Search & Comparison IntentPeople comparing contract roles in medical device developmentPeople seeking quality assurance contract roles in medical devices

Remote Contract Medical Device roles focus on product development, engineering, or technical support, while Remote Contract Medical Device Quality Assurance Specialists concentrate on compliance, audits, and quality management. Both are remote and industry-specific but serve different functions within the medical device sector.

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

The most popular types of Remote Medical Device jobs in Oregon are:

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

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

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

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

Infographic showing various Remote Contract Medical Device job openings in Oregon as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 16% Part Time, 6% Contract, and 1% Nights. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution.

Research Fellow, Medical Device Toxicologist

Bausch+Lomb Companies Inc.

OR โ€ข On-site, Remote

$150K - $200K/yr

Full-time

Dental, Vision, Life, Retirement, PTO

This job post hasย expired today.ย Applications are no longer accepted.


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 devicesย 
  • Ensures that development and execution of nonclinical strategies are aligned with product development and life cycle management activities, and with key regulatory expectations and milestonesย 
  • Ensures that essential nonclinical data are obtained, and effectively presented for successful clinical development, regulatory and quality compliance, market launch, and maintenance of businessย 
  • Coaches and mentors junior staffย 
  • Deep understanding of medical device relevant standards staying abreast of changes to applicable industry practice and guidance documents ย 
  • Implement new and revised standards into product development projects and/or assess impact on existing products as appropriateย 
  • Authors and reviews department's technical documents as neededย 
  • Manage interactions with other functions (e.g., Product Development, Clinical Development, Analytical Chemistry, Regulatory, Quality, Compliance)ย 
  • Liaise with company international offices on nonclinical safety matters for country-specific submissions/registrations and maintenance of business activitiesย 
  • Development and maintenance of department best practices and processesย 

Requirements:

  • Ph.D. in Toxicology or related discipline
  • 12+ years of relevant Medical Device industry experience
  • Experience managing a teamย 
  • DABT preferred
  • Ophthalmic medical device experience a plusย ย 

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.ย  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. basedย employeesย may be eligible forย short-term and/orย long-term incentives.ย They may also be eligible toย participateย in medical, dental, vision insurance, disability and life insurance, a 401(k) plan and company match, a tuition reimbursement program (select degrees), company holidays, andย well-beingย benefits, among others. U.S. based employees are also eligible to receive sick time, floating holidays and paid vacation.ย 

Job Applicants should be aware of job offer scams perpetrated through the use of the Internet and social media platforms.

To learn more please readย  Bausch + Lomb's Job Offer Fraud Statement.ย 

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.