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 ...
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 ...
Biocompatibility Program Manager
Hillsboro, OR · On-site
$90 - $120/hr
Proficiency with ISO-10993, ISO-14971, FDA and EU-MDR regulations and application to biocompatibility evaluations.- Familiarity to SAP, Windchill, CAD softwareWherever you're at in your career, our ...
Biocompatibility Program Manager
Hillsboro, OR · On-site
$90 - $120/hr
Proficiency with ISO-10993, ISO-14971, FDA and EU-MDR regulations and application to biocompatibility evaluations.- Familiarity to SAP, Windchill, CAD softwareWherever you're at in your career, our ...
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 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 ...
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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 ...
Proficiencywith ISO-10993, ISO-14971, FDA and EU-MDR regulations and application to biocompatibility evaluations. * Familiarity to SAP, Windchill, CAD software Following receipt of a conditional ...
Proficiencywith ISO-10993, ISO-14971, FDA and EU-MDR regulations and application to biocompatibility evaluations. * Familiarity to SAP, Windchill, CAD software Following receipt of a conditional ...
Principal, Pharmacovigilance / Device Vigilance
OR · On-site +1
Evaluate reportability of events under FDA (MDR), EU IVDR vigilance, Japan and other global regulations * Prepare and submit Medical Device Reports (MDRs) and vigilance reports within regulatory ...
Principal, Pharmacovigilance / Device Vigilance
OR · On-site +1
Evaluate reportability of events under FDA (MDR), EU IVDR vigilance, Japan and other global regulations * Prepare and submit Medical Device Reports (MDRs) and vigilance reports within regulatory ...
Proficiency with ISO-10993, ISO-14971, FDA and EU-MDR regulations and application to biocompatibility evaluations. * Familiarity to SAP, Windchill, CAD software Following receipt of a conditional ...
Proficiency with ISO-10993, ISO-14971, FDA and EU-MDR regulations and application to biocompatibility evaluations. * Familiarity to SAP, Windchill, CAD software Following receipt of a conditional ...
Own the endpoint security roadmap and drive execution across the environment, including migration off legacy tooling to a modern EDR/MDR stack. * Design and enforce identity and access controls ...
Own the endpoint security roadmap and drive execution across the environment, including migration off legacy tooling to a modern EDR/MDR stack. * Design and enforce identity and access controls ...
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 ...
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 ...
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 ...
Senior Quality Engineer - Redmond, OR
Redmond, OR · On-site
$101K - $152K/yr
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)
Senior Quality Engineer - Redmond, OR
Redmond, OR · On-site
$101K - $152K/yr
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 ...
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 ...
Senior Staff Medical Writer (Remote)
Portland, OR · On-site +1
$143K - $238K/yr
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 ...
Senior Staff Medical Writer (Remote)
Portland, OR · On-site +1
$143K - $238K/yr
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 ...
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 ...
Territory Channel Account Manager - NW Rockies Region
Portland, OR · On-site
$180 - $220/hr
Territory Channel Account Manager - NW Rockies Region About this position ThreatDown is a leader in elite Managed Detection and Response (MDR), purpose-built to empower resource-constrained security ...
Territory Channel Account Manager - NW Rockies Region
Portland, OR · On-site
$180 - $220/hr
Territory Channel Account Manager - NW Rockies Region About this position ThreatDown is a leader in elite Managed Detection and Response (MDR), purpose-built to empower resource-constrained security ...
Mdr information
See Oregon salary details
$19.57 - $24.51
4% of jobs
$24.51 - $29.46
3% of jobs
$29.46 - $34.40
0% of jobs
$34.40 - $39.35
7% of jobs
$40.73 is the 25th percentile. Wages below this are outliers.
$39.35 - $44.29
36% of jobs
$44.29 - $49.24
11% of jobs
$49.24 - $54.18
7% of jobs
$57.58 is the 75th percentile. Wages above this are outliers.
$54.18 - $59.13
9% of jobs
$59.13 - $64.07
10% of jobs
$64.07 - $69.01
9% of jobs
$69.01 - $73.96
4% of jobs
$19
$49
$73
How much do mdr jobs pay per hour?
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:
What job categories do people searching Mdr jobs in Oregon look for?
The top searched job categories for Mdr jobs in Oregon are:

Full-time
Posted 9 days ago
Job description
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