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Remote Medical Device Consulting Jobs (NOW HIRING)

Comfortable working with high accountability at a distributed, highly remote company with remote customers and daily interactions * Experience in healthcare, medical device, logistics, or regulated ...

PMP certification and prior medical device experience are preferred. * Reporting to: Technical ... Remote * Salary Range: $80,00-$105,000 annually + annual performance bonus * the final salary ...

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Remote Medical Coder III US Citizenship required. We are currently assembling a team of skilled ... consultations, and concurrent services, and inpatient surgical and anesthesia procedures; and ...

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Remote Medical Device Consulting information

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How much do remote medical device consulting jobs pay per hour?

As of Jun 12, 2026, the average hourly pay for remote medical device consulting in the United States is $49.84, according to ZipRecruiter salary data. Most workers in this role earn between $35.10 and $59.62 per hour, depending on experience, location, and employer.

What is the meaning of the word remote?

In the context of remote medical device consulting, 'remote' refers to performing work outside of a traditional office setting, often from a home or other location using digital communication tools. This allows consultants to collaborate with clients and teams virtually without being physically present at a specific site.

What is the meaning of remote in one word?

In the context of remote medical device consulting, 'remote' means working from a location outside the traditional office environment, often from home, using digital communication tools. It emphasizes flexibility and the use of technology to perform job duties without physical presence at a specific site.

How to make 2000 a week working from home?

Remote medical device consulting professionals can earn $2,000 or more weekly by leveraging specialized knowledge, certifications, and experience in regulatory compliance, quality assurance, or product development. Building a strong client base, maintaining high-quality work, and utilizing freelance platforms or direct networking can help achieve this income level while working from home.

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

Remote medical device consultants often face challenges such as coordinating with cross-functional teams in different time zones, staying updated with rapidly changing regulations, and ensuring thorough documentation without in-person oversight. Effective communication tools, regular virtual meetings, and a structured project management approach can help mitigate these issues. Additionally, leveraging secure digital platforms for document sharing and compliance tracking is essential to maintain productivity and regulatory standards in a remote setting.

What is remote medical device consulting?

Remote medical device consulting involves advising companies or individuals on the development, regulatory compliance, and market strategies for medical devices, all while working from a remote location. Consultants in this field may help with product design, FDA submissions, quality management systems, and international market entry. This role leverages virtual communication tools to collaborate with clients, making expertise accessible regardless of geographic barriers. The remote format allows for flexibility and can reduce costs for both consultants and clients.

What are the key skills and qualifications needed to thrive as a Remote Medical Device Consultant, and why are they important?

To thrive as a Remote Medical Device Consultant, you need a solid background in biomedical engineering, regulatory compliance, and clinical application of medical devices, often supported by a relevant degree and industry certifications. Familiarity with FDA regulations, ISO standards, and virtual collaboration tools like video conferencing and cloud document management is crucial. Strong problem-solving abilities, communication skills, and adaptability set exceptional consultants apart in remote environments. These skills and qualifications are vital to ensure effective client support, regulatory adherence, and successful project outcomes from a distance.

What is the best remote control for Alzheimer's patients?

Remote Medical Device Consulting professionals may recommend simplified, user-friendly remote controls designed for cognitive impairments, such as large buttons, clear labels, and minimal functions. These devices can help improve independence and safety for Alzheimer's patients and are often integrated with monitoring systems. Proper assessment and training are essential for effective use in a healthcare setting.
More about Remote Medical Device Consulting jobs
What cities are hiring for Remote Medical Device Consulting jobs? Cities with the most Remote Medical Device Consulting job openings:
What are the most commonly searched types of Medical Device Consulting jobs? The most popular types of Medical Device Consulting jobs are:
What states have the most Remote Medical Device Consulting jobs? States with the most job openings for Remote Medical Device Consulting jobs include:
Infographic showing various Remote Medical Device Consulting job openings in the United States as of June 2026, with employment types broken down into 4% Locum Tenens, 1% As Needed, 71% Full Time, 17% Part Time, and 7% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $103,662 per year, or $49.8 per hour.

Research Fellow, Medical Device Toxicologist

Bausch+Lomb Companies Inc.

OR • On-site, Remote

$150K - $200K/yr

Other

Dental, Vision, Life, Retirement, PTO

Posted 10 days ago


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. 

Our Benefit Programs: Employee Benefits: Bausch + Lomb

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.