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Mdr Jobs in Oregon (NOW HIRING)

Quality Engineer 2

Hillsboro, OR · On-site

$85 - $120/hr

Knowledge of FDA21CFR820, ISO13485, ISO14971, MDR/MDD, and related regulations. * Experience with CAPA, root cause analysis, Six Sigma, FMEA, DOE, risk analysis, statistical methods, and trend ...

Quality Engineer

Portland, OR · On-site

$76K - $98K/yr

May collaborate with Regulatory on Medical Device Reporting (MDR) and adverse event reporting requirements * Coordinate planning, implementation and trending of multiple quality management systems ...

Quality Assurance Specialist, Sr

Newberg, OR · Remote

$86K - $119K/yr

Achieves and maintains deep technical understanding of ISO 13485, 21 CFR 820, EU MDR and other medical device quality management and regulatory compliance standards as applicable. * Other duties as ...

Director, Clinical Development

OR · On-site +1

$75K - $102K/yr

Serve as the clinical voice on global regulatory submissions, ensuring strategic alignment with FDA, EU MDR/CE Mark, China (NMPA), and Japan (PMDA) regulatory pathways. * Design and oversee clinical ...

Experience applying knowledge of government and industry quality assurance codes and standards (e.g. 21 CFR 820, ISO13485, 21 CFR 210 and 211, MDD/MDR, and ANSI/AAMI/ISO sterilization standards)

Site Quality Leader

Wilsonville, OR · On-site

$136K - $170K/yr

This position is responsible for ensuring full compliance to the regulatory requirements of 21 CFR 820, ISO13485, MDR and other applicable regulations including production and process controls. The ...

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 ...

Quality Assurance Specialist, Sr

Newberg, OR · On-site

$86K - $119K/yr

Achieves and maintains deep technical understanding of ISO 13485, 21 CFR 820, EU MDR and other medical device quality management and regulatory compliance standards as applicable. * Other duties as ...

Mdr information

See Oregon salary details

$19

$49

$73

How much do mdr jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for mdr in Oregon is $49.89, according to ZipRecruiter salary data. Most workers in this role earn between $40.91 and $59.71 per hour, depending on experience, location, and employer.

What is an MDR?

An MDR (Market Development Representative) is a sales professional responsible for identifying and qualifying potential leads for a company's products or services. They focus on early-stage prospecting, researching target markets, and engaging with potential customers to generate sales opportunities. MDRs work closely with sales and marketing teams to ensure a seamless handoff of qualified leads for further nurturing and closing. Their role is crucial in driving business growth by expanding the company's customer base.

What does a typical day look like for a Medical Device Reprocessing (MDR) technician?

A typical day for an MDR Technician involves cleaning, disinfecting, and sterilizing surgical instruments and medical devices according to strict protocols. You'll routinely inspect equipment, assemble instrument trays, document processes, and ensure all items meet quality assurance standards. MDR Technicians frequently collaborate with surgical teams and other healthcare professionals to meet tight turnaround times for critical instruments. This is a hands-on role that requires adaptability, precision, and a commitment to patient safety, often performed in hospital central sterile departments or specialized clinics.

What are the key skills and qualifications needed to thrive in the MDR position, and why are they important?

To thrive as a Medical Device Reprocessing (MDR) Technician, you need knowledge of sterilization processes, infection control standards, and a high school diploma or equivalent, often supplemented with formal MDR certification. Familiarity with autoclaves, washer-disinfectors, and tracking systems is necessary for proper equipment handling. Attention to detail, teamwork, and effective communication are important soft skills in this role. These abilities ensure patient safety and efficient support of clinical procedures in healthcare environments.

What are popular job titles related to Mdr jobs in Oregon?

For Mdr jobs in Oregon, the most frequently searched job titles are:

Infographic showing various Mdr job openings in Oregon as of August 2026, with employment types broken down into 89% Full Time, 7% Part Time, and 4% Contract. Highlights an 77% Physical, 7% Hybrid, and 16% Remote job distribution, with an average salary of $103,767 per year, or $49.9 per hour.

Medical Systems Engineer - Mechanical

Biotronik

Lake Oswego, OR • On-site

Full-time

Posted 9 days ago


Job description

Working for Micro Systems Engineering, Inc. (MSEI) means joining an elite team to work on some of the most exciting challenges in medical technology today. We are a pioneer in developing innovative implantable medical device technologies and devices that save and enhance the quality of life for millions of individuals living with cardiovascular and chronic neurologic pain disorders. With more than 40 years of experience in design and manufacturing of active implantable medical devices, our continuing success is based on our company's core values - innovation, quality, reliability, integrity, teamwork, and undisputed expertise - thus enabling us to inspire confidence and trust in physicians and patients worldwide. We are continually looking for talented engineers, scientists, and professionals to share in our mission.
Please join us as:
Medical Systems Engineer - Mechanical
We are seeking a Systems Engineer - Mechanical Engineer to join our R&D team. This role places you at the technical center of development of complex implantable medical devices focusing on the design of mechanical aspects of active implantable devices and their accessories. The role involves collaboration across multidisciplinary teams including mechanical, electrical and software teams. This role involves contributions from prototype phases through verification and validation, all the way to post-market product support.
Key Responsibilities
System Design & Integration
  • Lead mechanical design and system integration of implantable and accessory devices.
  • Define and manage subsystem requirements and interfaces.
  • Collaborate with electrical, manufacturing and human factors engineering teams to ensure cohesive system design.

Prototyping & Development
  • Support rapid prototyping, including 3D printing and bench testing.
  • Apply iterative development methods to refine mechanical components.
  • Verification, Validation & Testing
  • Develop and execute test plans to ensure compliance with performance, safety, and regulatory requirements.
  • Support and lead risk management activities, including FMEA, fault tree analysis, and root cause investigations.
  • Regulatory & Standards Compliance
  • Ensure design activities comply with relevant standards (e.g., IEC 60601, ISO 14971, FDA QSR, EU MDR).
  • Document system behavior and design decisions in line with regulatory expectations.

Post-Market Engineering
  • Provide technical support for released products, including root cause analysis and implementation of design improvements.
  • Analyze field and product performance data to drive continuous improvement.

Your Profile
Education
  • Bachelor's Degree or higher in a technical field such as Mechanical Engineering, Biomedical Engineering, or a related discipline.
  • Work Experience
  • Industry Experience: Minimum 5 years of experience in mechanical or systems engineering and preferably:
    • Experience with neurostimulation or other similar active implantable devices.
    • Exposure to manufacturing processes for implantable devices.
    • Understanding of human factors and usability engineering in medical systems.

Desired Technical Skills & Competencies:
  • Proficient in mechanical design and CAD (Solidworks or similar)
  • Experience with mechanical prototyping and 3D printing.
  • Knowledge of verification and validation practices (Design & Process V&V).
  • Understanding of biocompatibility testing and materials for implantable
  • Proficiency in at least one data processing, scripting and plotting software (e.g. VS Code, Matlab, python)
  • Experience writing technical documents and working drawings for manufacturing
  • Experience working with regulatory standards such as ISO 14708, IEC 60601, FDA 21 CFR 820.11, MDR and ISO 14971.
  • Experience working in requirements management tools
  • Project Management Skills: Proven ability to organize, prioritize, and execute multiple projects in a fast-paced, detail-oriented environment.
  • Communication & Teamwork: Strong interpersonal and communication skills, with the ability to effectively collaborate across teams and present complex ideas clearly.
  • Ability to prioritize effectively and work on concurrent projects.
  • Excellent problem-solving and analytical skills.
  • Strong communication and interpersonal skills including technical report writing skills.

Location
  • Lake Oswego, OR this is a hybrid position.

Location: Lake Oswego(0001)
Working hours: Full-time
MSEI Lake Oswego Oregon (US-OR) USA
Job ID: 62396
Micro Systems Engineering, Inc. is an equal opportunity employer. In accordance with applicable law, the company prohibits discrimination based on race, color, religion, creed, gender, pregnancy or related medical conditions, age, national origin or ancestry, physical or mental disability, sexual orientation, genetic information, uniformed service or any other consideration protected by federal state and local laws. Our commitment to equal opportunity employment applies to all persons involved in our operations and prohibits unlawful discrimination by any employee