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Contract Quality Engineer Medical Device Jobs in Oregon

Quality Engineer

Mcminnville, OR · Hybrid

$73K - $94K/yr

Experience working in aerospace, defense, medical device, or similar highly regulated industries ... Job Type & Location This is a Contract to Hire position based out of McMinnville, OR. Pay and ...

Follow standard operating procedures (SOPs) to ensure compliance with FDA, GMP, and quality system ... Schedule: 1st Shift:- 4:00 AM to 2:30 PM - Monday to Thursday This is a Full-time, Contract ...

Manufacturing Quality Engineer

Newberg, OR

$78K - $100K/yr

Familiarity with quality standards relevant to aerospace, defense, medical device, or similar ... Contract to Hire position based out of Newberg, OR. Pay and Benefits The pay range for this ...

Quality Engineer

Hood River, OR · On-site

$75 - $105/hr

Quality Engineer Full Time Professional Hood River, OR, US Purpose of Position: The Quality ... Effective use of computer, laptop, cell phone and other mobile device to exchange information.

Quality Engineer

Sherwood, OR

$77K - $100K/yr

... customer contracts. * Serve as an active member of the Material Review Board (MRB), leading or ... Prior experience supporting aerospace, defense, medical, or semiconductor customer Job Conditions ...

Quality Engineer

Sherwood, OR · On-site

$85 - $120/hr

... customer contracts. * Serve as an active member of the Material Review Board (MRB), leading or ... Prior experience supporting aerospace, defense, medical, or semiconductor customer Job Conditions ...

Quality Engineer

Tualatin, OR · On-site

$80K - $100K/yr

Ascentec Engineering is seeking a Quality Engineer to support our Machining and Integrated Assembly ... Paid medical coverage * Short- and long-term disability coverage * 401(k) with matching funds

Quality Engineer

Tualatin, OR · On-site

$80K - $100K/yr

Description: Ascentec Engineering is seeking a Quality Engineer to support our Machining and ... Paid medical coverage * Short- and long-term disability coverage * 401(k) with matching funds

Quality Engineer

White City, OR · On-site

$72K - $93K/yr

Emerald Technologies is seeking a Quality Engineer who is analytical, solutions‑driven, and ... Competitive medical, dental, and vision benefits  * Health Savings Account/Flexible Spending ...

Quality Engineer

Canby, OR · On-site

$75K - $97K/yr

... contract electronics manufacturer with over 70 years of experience bringing innovations to life ... As a Quality Engineer at our Canby, OR facility, you'll be embedded in the production process ...

Quality Engineer

Canby, OR · On-site

$70 - $90/hr

... contract electronics manufacturer with over 70 years of experience bringing innovations to life ... As a Quality Engineer at our Canby, OR facility, you'll be embedded in the production process ...

Quality Engineer

Canby, OR

$75K - $97K/yr

... contract electronics manufacturer with over 70 years of experience bringing innovations to life ... As a Quality Engineer at our Canby, OR facility, you'll be embedded in the production process ...

Quality Engineer

Canby, OR · On-site

$75K - $97K/yr

... contract electronics manufacturer with over 70 years of experience bringing innovations to life ... As a Quality Engineer at our Canby, OR facility, you'll be embedded in the production process ...

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Showing results 1-20

Contract Quality Engineer Medical Device information

What does a contract quality engineer do in the medical device industry?

A Contract Quality Engineer in the medical device industry is responsible for ensuring that products meet regulatory and company quality standards during a specific project or timeframe. They typically work on a contract basis, focusing on tasks like process validation, risk management, root cause analysis, and compliance with standards such as ISO 13485 and FDA regulations. Their role often involves collaborating with engineering, production, and regulatory teams to troubleshoot quality issues and implement corrective actions. They play a key role in maintaining product safety and regulatory compliance throughout the manufacturing process.

What are the key skills and qualifications needed to thrive as a contract quality engineer in the medical device industry?

To thrive as a Contract Quality Engineer in the Medical Device field, you need expertise in quality assurance, regulatory compliance (such as ISO 13485 and FDA regulations), and a background in engineering or life sciences. Familiarity with tools like CAPA systems, risk management software, and proficiency in quality management systems (QMS) is typically required. Strong analytical thinking, attention to detail, and effective communication skills set top performers apart in this role. These skills are essential to ensure product safety, regulatory compliance, and the successful launch and maintenance of medical devices in a highly regulated environment.

How does a contract quality engineer in the medical device industry typically collaborate with cross-functional teams?

As a Contract Quality Engineer in the medical device sector, you will frequently work closely with cross-functional teams, including R&D, manufacturing, regulatory affairs, and supply chain. Your responsibilities often involve reviewing design documentation, participating in risk assessments, and ensuring production processes meet both internal quality standards and regulatory requirements. Effective communication is key, as you'll be responsible for conveying quality expectations, addressing non-conformities, and supporting project timelines. This collaborative environment provides valuable experience in coordinating with diverse professionals while upholding strict industry standards.

What is the difference between Contract Quality Engineer Medical Device vs Contract Quality Engineer Pharmaceutical?

AspectContract Quality Engineer Medical DeviceContract Quality Engineer Pharmaceutical
CertificationsISO 13485, FDA QSR, GMPICH Q7, GMP, FDA regulations
Work EnvironmentMedical device manufacturing, labs, compliance auditsPharmaceutical production, labs, quality assurance
Industry UsageMedical device companies, OEMs, suppliersPharmaceutical firms, biotech companies, contract manufacturers

Both roles focus on quality assurance and regulatory compliance but differ mainly in industry-specific standards and environments. Contract Quality Engineers Medical Device work primarily with ISO 13485 and FDA QSR standards in device manufacturing, while Contract Quality Engineers Pharmaceutical focus on GMP and ICH Q7 regulations in drug production. Understanding these differences helps candidates target the right industry and certifications for their career goals.

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

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

What are popular job titles related to Contract Quality Engineer Medical Device jobs in Oregon?

For Contract Quality Engineer Medical Device jobs in Oregon, the most frequently searched job titles are:

What cities in Oregon are hiring for Contract Quality Engineer Medical Device jobs?

Cities in Oregon with the most Contract Quality Engineer Medical Device job openings:

Infographic showing various Contract Quality Engineer Medical Device job openings in Oregon as of July 2026, with employment types broken down into 65% Full Time, 18% Part Time, 1% Temporary, and 16% Contract. Highlights an 78% Physical, 3% Hybrid, and 19% Remote job distribution.

Senior Electrical Engineer - Medical Device Electronics

Newberg, OR • On-site


A-dec, Inc. (USA)

8.8

Company rating: 8.8 out of 10

Based on 13 frontline employees who took The Breakroom Quiz

3rd of 52 rated furniture manufacturers

People enjoy working here

Good employer

Paid breaks


$75 - $95/hr

Other

Posted 8 days ago


Job description

A-dec, Inc. (USA) is seeking an Electrical Engineer to work on project assignments in the design and integration of components for industry-leading dental equipment. This role requires effective communication skills, the ability to manage engineering projects, and a Bachelor's degree in engineering.

With a focus on design analysis, PCB creation, and ensuring compliance with medical device standards, candidates should possess at least five years of engineering experience and the capability to direct project tasks. A-dec is committed to providing a supportive and innovative work environment.

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