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Remote Medical Device Consulting Jobs in Oregon (NOW HIRING)

Centene

Remote Medical Director, Appeals

OR · On-site +1

$236K - $449K/yr

... medical and pharmacy consultants for reviewing complex cases and medical necessity appeals ... with remote, hybrid, field or office work schedules. Actual pay will be adjusted based on an ...

ARTHREX

Learning Experience Designer - Remote

OR · Remote

$66K - $90K/yr

Salary Minimum: $66,000 Salary Maximum: $90,000 Arthrex, Inc. is a global medical device company ... This role manages the end-to-end design process, from needs analysis and performance consulting to ...

New

A-dec, Inc.

Quality Assurance Specialist, Sr

Newberg, OR · Remote

$86K - $119K/yr

... Medical Device regulations and standards including US-FDA, Health Canada, and the European Union ... Fully remote is not an option due to manufacturing facility-based activities. Education and ...

NV5

Remote Sensing Technician

NV5 is a global technology solutions and consulting services company with a workforce of over 4,500 ... NV5 offers competitive compensation and benefits package including medical, dental, life insurance ...

ARTHREX

Installation Project Specialist - Synergy

OR · On-site +1

$73K - $100K/yr

Remote available for the right candidate.* *Project work is mostly in East Coast and Midwest locations* Arthrex, Inc. is a global medical device company and a leader in new product development and ...

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Remote Medical Device Consulting information

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 are popular job titles related to Remote Medical Device Consulting jobs in Oregon? For Remote Medical Device Consulting jobs in Oregon, the most frequently searched job titles are:
What job categories do people searching Remote Medical Device Consulting jobs in Oregon look for? The top searched job categories for Remote Medical Device Consulting jobs in Oregon are:
What cities in Oregon are hiring for Remote Medical Device Consulting jobs? Cities in Oregon with the most Remote Medical Device Consulting job openings:
Remote Medical Device Consulting jobs near you

Research Fellow, Medical Device Toxicologist

Bausch + Lomb

OR • On-site, Remote

$150K - $200K/yr

Full-time

Medical, Retirement, PTO

Re-posted 27 days ago

Bausch & Lomb rating

8.6

Company rating: 8.6 out of 10

Based on 39 frontline employees who took The Breakroom Quiz

25th of 536 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.
What We Offer:
  • Comprehensive health, wellness, and retirement benefits.
  • Paid time off and programs that support work-life balance.
  • Opportunities to learn, grow, and contribute to meaningful work.

Check out our US benefits here - Employee Benefits: Bausch + Lomb
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

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