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Medical Device Design Jobs in Oregon (NOW HIRING)

Compact Device Modeling Group (CDMG) is part of Intel's Design Technology Platform (DTP ... Candidates should never be required to pay recruitment fees, medical examination fees, or any other ...

Medical device and mechanical system design * Biosensors, optical monitoring, and signal filtering * Real-time data acquisition and control systems * Precision and sterile manufacturing environments

Medical device and mechanical system design * Biosensors, optical monitoring, and signal filtering * Real-time data acquisition and control systems * Precision and sterile manufacturing environments

Senior Program Manager

OR ยท On-site +1

$115K - $116K/yr

Deep practical understanding of ISO 13485, IEC 62304, design controls, and medical device/IVD development processes. * Experience leading teams through design reviews, phase exits, development ...

We are a pioneer in developing innovative implantable medical device technologies and devices that ... With more than 40 years of experience in design and manufacturing of active implantable medical ...

Strong preference for experience leading new product development programs within the medical device industry, including a strong understanding of Design Controls and regulated product development ...

Strong preference for experience leading new product development programs within the medical device industry, including a strong understanding of Design Controls and regulated product development ...

Showing results 21-40

Medical Device Design information

See Oregon salary details

$22

$52

$102

How much do medical device design jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for medical device design in Oregon is $52.69, according to ZipRecruiter salary data. Most workers in this role earn between $37.12 and $63.03 per hour, depending on experience, location, and employer.

What is a medical device design?

A Medical Device Design job involves creating, developing, and improving medical devices to ensure they are safe, effective, and user-friendly. Professionals in this field work with engineers, regulatory specialists, and healthcare professionals to meet industry standards and patient needs. They use computer-aided design (CAD) software, prototyping, and testing methodologies to refine devices before production. The role requires knowledge of biomechanics, materials science, and regulatory guidelines such as FDA and ISO standards.

What are some typical challenges faced in a medical device design role?

Medical Device Design professionals often encounter challenges such as balancing innovative design with stringent regulatory requirements and ensuring devices are both effective and safe for patient use. Navigating complex approval processes, collaborating with clinicians for feedback, and keeping up with rapidly evolving technologies can also be demanding. However, these challenges make the role dynamic and rewarding, as designers play a direct role in improving patient outcomes. Team-based problem solving and ongoing learning are key parts of the job, and successfully overcoming challenges can lead to career growth and leadership opportunities within the medical device industry.

What are the key skills and qualifications needed to thrive in medical device design, and why are they important?

Success in Medical Device Design requires a solid understanding of biomedical engineering, materials science, and human anatomy, often supported by a relevant engineering degree and experience in product development. Familiarity with CAD software, rapid prototyping tools, and regulatory standards such as FDA or ISO 13485 certification is common in the field. Strong problem-solving abilities, teamwork, and effective communication help professionals excel in multidisciplinary design teams. These competencies are crucial for creating safe, innovative medical devices that meet strict quality and regulatory requirements.

What are the most commonly searched types of Medical Device Design jobs in Oregon?

The most popular types of Medical Device Design jobs in Oregon are:

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

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

What job categories do people searching Medical Device Design jobs in Oregon look for?

The top searched job categories for Medical Device Design jobs in Oregon are:

Infographic showing various Medical Device Design job openings in Oregon as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 18% Part Time, and 6% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $109,600 per year, or $52.7 per hour.

Project Manager, NRO Development

BIOTRONIK SE & Co.KG

Lake Oswego, OR โ€ข On-site

$100 - $135/hr

Other

Posted 3 days ago

New


Job description

Requisition ID62508-Posted08/28/2026- Posting Country (1) - Work Location (1) -Engineering-Undefined-Full-time-Professionals-MST

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 companyโ€™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:

Project Manager, NRO Development

SUMMARY

The Project Manager will coordinate New Technology and New Product Development efforts, consistent with medical device new product develpment customer requirements. The Project Manager will interface with Senior Management, Line Management, and external customers and supplier to assure success against Key Performance Indicators.

PRIMARY JOB RESPONSIBILITIES
  • Manages international development teams to assure technology and development efforts are achieved in alignment with established project and portfolio commitments.
  • Develops and manages project plans, schedules, and budgets for NPD and technology projects.
  • Develops and maintains strong relationship with internal and external suppliers. Lead the effort to identify, evaluate, and select relevant suppliers to meet project goals.
  • Interacts with internal and external customers to assure scope of projects meet Voice-of-Customer needs.
  • Provides regular updates to Senior Management, Product Management, Operations, and other departments to assure project deliverables are on track with intended goals. Using relevant KPIs, provides risk-based analysis of project to assure that project goals are met within constraints of given budgets and timelines.
  • Works with Design and Quality assurance, leading the effort to assure medical devices are developed in compliance with relevant Quality Management Systems. May assist with product and QM audits, as necessary.
  • Other duties may be assigned at the discretion of the manager.
REQUIRED QUALIFICATIONS
  • BS Degree in engineering in the field of Electrical, Biomedical, Mechanical, or related engineering discipline.
  • Minimum 4 yearsโ€™ experience in project management of medical devices or similarly regulated industry.
  • Experience in project management of international and global development teams.
  • Demonstrated track record of technical project management leadership.
  • Strong communication skills, with a focus on team collaboration/development.
  • Strong group facilitation and mediation skills.
  • Industry-related knowledge of medical device development.
PREFERRED QUALIFICATIONS
  • PMP or similar certification.
  • Familiarity with Agile and other project management methodologies.
  • Direct knowledge of FDA and MDR regulations.
  • Experience with ISO 13485 and/or 21CFR820 compliant Quality Management Systems.
LEADERSHIP RESPONSIBILITIES

Work with MST customers as project liaison between the development team and stakeholders.
Coordinate with team leads to drive project and establish estimates of project time and materials.
No direct personnel management required.

TRAVEL REQUIREMENTS

Must be able to travel internationally and domestically, less than 15% of the time.

WORK ENVIRONMENT

If onsite, this role is based in a temperature controlled professional office setting, which may include an office or cubicle with quiet to moderate noise level. If remote, the work environment is the employeeโ€™s residence. Work may need to be completed on campus in a lab, or manufacturing environment such as clean room or warehouse. Personal protective equipment is required in the clean room and may be needed in a lab. The noise level in the lab, and manufacturing environments are quiet to moderate. The role may travel to vendors, customers, external training, expos, industry or product events, and networking events shifting the work environment.

This position is Hybrid, based in out Lake Oswego, Oregon office.

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, nationaloriginor 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.

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