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Remote Medical Device Assembler Jobs in Oregon (NOW HIRING)

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 ...

Enterprise Account Executive

OR · On-site +1

$200K - $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.

Strategic Account Executive

OR · On-site +1

$250K - $360K/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.

Growth Account Executive

OR · On-site +1

$150K - $200K/yr

... Medical Device Industry. Our Commercial Team takes a proactive, consultative, and high-touch ... Remote work : AcuityMD is committed to supporting full-remote flexibility for employees in the US.

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 ...

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 ...

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 ...

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 ...

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 ...

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Remote Medical Device Assembler information

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

As of Sep 5, 2026, the average hourly pay for remote medical device assembler in Oregon is $20.75, according to ZipRecruiter salary data. Most workers in this role earn between $18.32 and $22.36 per hour, depending on experience, location, and employer.

What is a remote medical device assembler?

A Remote Medical Device Assembler is responsible for assembling, inspecting, and testing medical devices from a remote or home-based location. They follow strict guidelines and quality control procedures to ensure the devices meet safety and regulatory standards. This role may involve working with small components, using specialized tools, and documenting production processes. Strong attention to detail, manual dexterity, and adherence to industry regulations are essential for success in this role.

What does a remote medical device assembler do?

As a Remote Medical Device Assembler, your day often starts with virtual team check-ins to review production goals and clarify any assembly procedures. Your core responsibility is to carefully assemble and inspect medical device components, following detailed work instructions and quality protocols, all while maintaining meticulous documentation. You will collaborate with supervisors, engineers, and quality assurance staff through video conferencing and instant messaging platforms to resolve questions or alert the team to potential issues. Adapting to a remote workflow, you'll need to manage your time independently while meeting productivity and quality targets. This role requires self-discipline and proactive communication to ensure all devices meet stringent medical standards.

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

To thrive as a Remote Medical Device Assembler, you need strong manual dexterity, attention to detail, and familiarity with assembly processes, typically supported by a high school diploma or equivalent. Experience with remote collaboration platforms, basic ERP or inventory systems, and understanding of Good Manufacturing Practices (GMP) is beneficial. Strong organizational skills, self-motivation, and clear communication are vital soft skills for succeeding in a remote environment. These capabilities ensure high-quality device assembly, compliance with regulatory standards, and effective teamwork despite working remotely.

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

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

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

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

Infographic showing various Remote Medical Device Assembler job openings in Oregon as of August 2026, with employment types broken down into 1% As Needed, 66% Full Time, 28% Part Time, and 5% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $43,151 per year, or $20.7 per hour.

Medical Device & Diagnostics - CRA 2 - US Remote

Fortrea

OR • On-site, Remote

$105/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 7 days ago


Fortrea rating

8.3

Company rating: 8.3 out of 10

Based on 11 frontline employees who took The Breakroom Quiz

29th of 75 rated research


Job description

We are currently seeking Experienced Device CRA 2s to lead and support our Medical Device & Diagnostics team! Open to major hub locations across the US. 60-70% travel, 7-9 DOS per month.

WHAT YOU WILL DO

You will utilize your skills, knowledge, and clinical judgement to provide a high standard of care for participants in clinical trials and respond to emergency situations based upon clinical research standards.

Responsibilities:

  • Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned -
  • Responsible for all aspects of site management as prescribed in the project plans
  • General On-Site Monitoring
  • Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study
  • Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements
  • Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data
  • Responsible for all aspects of registry management as prescribed in the project plans - Undertake feasibility work when requested
  • Complete Serious Adverse Event (SAE) reporting, process production of repo11s, narratives and follow up of SAEs
  • Independently perform CRF review; query generation and resolution against established data review guidelines on Fortrea or client data management systems as assigned by management
  • Assist with training of new employees, eg. co-monitoring
  • Coordinate designated clinical projects as a Local Project Coordinator (with supervision, ifapplicable) and may act as a local client contact as assigned
  • Perform other duties as assigned by management

Requirements

  • University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g. nursing licensure)
  • 1-3 years of Clinical Monitoring experience
  • Open to various hub locations

The important thing for us is you are comfortable working in an environment that is:

  • Fast paced: where no deviations from the study protocol are allowed, and not meeting a timeline for even few minutes will create a quality issue.
  • Changing priorities constantly asking you to prioritize and adapt on the spot.
  • Teamwork and people skills are essential for the study to run smoothly.
  • Technology based. We collect our data directly into an electronic environment.

What do you get?

Regular, full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including but not limited to:

  • Medical, Dental, Vision, Life, STD/LTD (multiple insurance carriers)
  • 401(K)
  • Paid time off (PTO) - Flex Plan
  • Employee recognition awards
  • Multiple ERG's (employee resource groups)
  • Target Pay Range (based on title): $105-117K

Work Environment:

  • Work is performed in an office environment with exposure to electrical office equipment.
  • Frequent travel to clients/ site locations with occasional travel both domestic and international.

Physical Requirements:

  • Ability to sit for extended periods and operate a vehicle safely.
  • Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists.
  • Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.
  • Ability to access and use a variety of computer software developed both in-house and off-the-shelf.
  • Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.
  • Regular and consistent attendance.
  • Varied hours may be required.

#LI - Remote

Applications will be accepted on an ongoing basis.

Learn more about our EEO & Accommodations request here.


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