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Remote 3D Product Visualization Jobs in Portland, OR

Stryker

Senior Staff Medical Writer (Remote)

Portland, OR · On-site +1

$143K - $238K/yr

... visualization, connected OR solutions, sports medicine products to sustainability solutions. As the Senior Staff Medical Writer , you will develop scientific and clinical documentation that supports ...

McKinstry

BIM Professional

Portland, OR · On-site +1

$33.58 - $49.24/hr

Promotes best practices to improve production efficiency in Revit. * Assists in developing complex ... Performs 2D and 3D drafting in Revit. * Updates backgrounds and models per project schedule. * Uses ...

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All Jobs3D Product Visualization JobsRemote 3D Product Visualization JobsRemote 3D Product Visualization Jobs in Portland, OR

Remote 3D Product Visualization information

See Portland, OR salary details

$56.2K

$152.8K

$217.4K

How much do remote 3d product visualization jobs pay per year?

As of Sep 12, 2026, the average yearly pay for remote 3d product visualization in Portland, OR is $152,789.00, according to ZipRecruiter salary data. Most workers in this role earn between $93,300.00 and $217,400.00 per year, depending on experience, location, and employer.

What is remote 3D product visualization?

Remote 3D product visualization is the process of creating and viewing realistic, interactive 3D models of products using specialized software, often from a location outside of a traditional office or studio. Professionals in this field use tools like Blender, Autodesk 3ds Max, or Unity to design and render product images and animations for marketing, prototyping, or e-commerce. The 'remote' aspect means that the work can be done from anywhere with a computer and internet connection, allowing for flexible collaboration with clients and teams globally.

What are the key skills and qualifications needed to thrive as a remote 3D product visualization specialist?

To thrive as a Remote 3D Product Visualization Specialist, you need strong expertise in 3D modeling, rendering, and a solid understanding of product design principles, often supported by a degree in design, computer graphics, or a related field. Proficiency with technical tools such as Autodesk 3ds Max, Blender, Cinema 4D, V-Ray, and Adobe Creative Suite is typically required. Excellent communication, time management, and attention to detail help you collaborate effectively with remote teams and clients. These skills are crucial to producing high-quality, accurate visual content that meets client expectations and drives project success in a remote work environment.

What are the typical challenges faced when working remotely as a 3D product visualization specialist, and how can they be managed?

Remote 3D Product Visualization specialists often encounter challenges such as coordinating across different time zones with clients or team members, ensuring clear communication about design revisions, and handling large file transfers or software compatibility issues. Effective project management tools, regular video calls, and clear documentation can help mitigate misunderstandings. Additionally, utilizing cloud-based collaboration platforms and maintaining a reliable, high-performance workstation are essential for smooth workflows and meeting project deadlines.

What are the most commonly searched types of 3D Product Visualization jobs in Portland, OR?

The most popular types of 3D Product Visualization jobs in Portland, OR are:

What are popular job titles related to Remote 3D Product Visualization jobs in Portland, OR?

For Remote 3D Product Visualization jobs in Portland, OR, the most frequently searched job titles are:

What job categories do people searching Remote 3D Product Visualization jobs in Portland, OR look for?

The top searched job categories for Remote 3D Product Visualization jobs in Portland, OR are:

Remote 3D Product Visualization jobs near you
Infographic showing various Remote 3D Product Visualization job openings in Portland, OR as of August 2026, with employment types broken down into 92% Full Time, and 8% Part Time. Highlights an 100% Remote job distribution, with an average salary of $152,789 per year, or $73.5 per hour.

Senior Staff Medical Writer (Remote)

Portland, OR • On-site, Remote

Stryker
Medical Equipment and Supplies Manufacturing • 10K+ employees
Learn more about Strykerexternal

$143K - $238K/yr

Full-time

Posted 26 days ago

Key responsibilities

  • Author and maintain clinical and regulatory documentation such as Clinical Evaluation Reports (CERs) and Post-Market Clinical Follow-Up (PMCF) documents.

  • Compile, analyze, and synthesize clinical evidence from various sources into submission-ready regulatory documents.

  • Collaborate with cross-functional teams to develop clinical evidence strategies, regulatory documentation plans, and project timelines.

Stryker rating

8.2

Company rating: 8.2 out of 10

Based on 112 frontline employees who took The Breakroom Quiz

Job description

Work Flexibility: Remote

Stryker is hiring a Senior Staff Medical Writer to join our Endoscopy Division, to be based remotely anywhere within the United States. Stryker is one of the world's leading medical technology companies and, together with its customers, is driven to make healthcare better. Our Endoscopy Division delivers a diverse array of innovative medical technologies to support minimal invasive surgery through brilliant visualization, connected OR solutions, sports medicine products to sustainability solutions.

As the Senior Staff Medical Writer, you will develop scientific and clinical documentation that supports global regulatory compliance and market access for medical devices. This position partners closely with Regulatory Affairs, Clinical Affairs, Quality, Research & Development, and Marketing teams to translate complex clinical evidence into high-quality regulatory and scientific documents throughout the product lifecycle.

What You Will Do

  • Author and maintain Clinical Evaluation Reports (CERs), Post-Market Clinical Follow-Up (PMCF) documents, and other clinical evidence documentation supporting international product registrations and lifecycle management.

  • Compile, analyze, and synthesize clinical evidence from clinical studies, published literature, post-market data, and other safety and performance sources into submission-ready regulatory documents.

  • Respond to notified body reviews and regulatory feedback, driving resolution of clinical documentation questions to support ongoing market access.

  • Collaborate with cross-functional teams to develop clinical evidence strategies, regulatory documentation plans, and project timelines.

  • Author clinical study protocols, study reports, data summaries, and supporting scientific documents for regulatory and clinical initiatives.

  • Conduct systematic literature reviews, evaluate scientific data, and integrate findings into clinical and regulatory documentation.

  • Lead document review cycles, coordinate stakeholder feedback, resolve content issues, and obtain timely approvals.

  • Drive continuous improvement initiatives, maintain medical writing tools and templates, and mentor junior medical writing team members.

What You Need

Required

  • Bachelor's degree in a scientific, technical, healthcare, or related discipline.

  • Minimum 6 years of industry experience within medical technology, medical devices, pharmaceuticals, or healthcare products.

  • Minimum 4 years of experience in scientific writing, medical writing, clinical research, or related regulatory documentation activities.

  • Experience authoring Clinical Evaluation Reports (CERs) and Post-Market Clinical Follow-Up (PMCF) documentation.

  • Expert knowledge of MEDDEV 2.7/1 Rev. 4, European Union Medical Device Regulation (EU MDR 2017/745), and Medical Device Coordination Group (MDCG) guidance for clinical evaluations.

  • Experience conducting systematic literature reviews and utilizing scientific databases, literature search methodologies, and literature management tools.

  • Knowledge of FDA, Good Clinical Practice (GCP), ISO 14155, ISO 14971, and applicable international medical device regulations and standards.

Preferred

  • Master's degree, PhD, PharmD, MD, MPH, RN, BSN, or other advanced health-related degree.

  • Experience authoring clinical study protocols, clinical study reports, manuscripts, or scientific publications.

  • Experience supporting regulatory submissions and global market access initiatives for medical devices.

  • Knowledge of clinical operations, risk management, and international regulatory requirements.

United States of America Pay Ranges:

  • USN: $110,100 - $183,400 USD Annual
  • US5: $115,600 - $192,600 USD Annual
  • US10: $121,100 - $201,700 USD Annual
  • US15: $126,600 - $210,900 USD Annual
  • US20: $132,100 - $220,100 USD Annual
  • US30: $143,100 - $238,400 USD Annual
View the U.S. work location and transparency guide to find the pay range for your location.

Travel Percentage: 10%Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information.

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