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Software Qa Engineer Intern Jobs in Portland, OR

Manager, QA Engineering

Hillsboro, OR · On-site

$129.60 - $194.40/hr

Define and implement an effective software quality assurance strategy aligned with business and ... Familiarity with Semi SECS/GEM standards, database validation, and programming languages, such as ...

Define and implement an effective software quality assurance strategy aligned with business and ... Familiarity with Semi SECS/GEM standards, database validation, and programming languages, such as ...

Manager, QA Engineering

Hillsboro, OR · On-site

$129K - $194K/yr

Define and implement an effective software quality assurance strategy aligned with business and ... Familiarity with Semi SECS/GEM standards, database validation, and programming languages, such as ...

About the Role We are looking for a motivated QA / Test Automation Engineer (Embedded SDET) who is eager to build a career in embedded systems testing and automation. This is an excellent opportunity ...

Bachelor's degree in computer science, Engineering, or related field (or equivalent experience) * 8+ years of experience in software Quality Assurance and Testing * Thorough understanding of Software ...

Bachelor's degree in computer science, Engineering, or related field (or equivalent experience) * 8+ years of experience in software Quality Assurance and Testing * Thorough understanding of Software ...

Bachelor's degree in computer science, Engineering, or related field (or equivalent experience) * 8+ years of experience in software Quality Assurance and Testing * Thorough understanding of Software ...

Showing results 21-40

Software Qa Engineer Intern information

See Portland, OR salary details

$14

$26

$41

How much do software qa engineer intern jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for software qa engineer intern in Portland, OR is $26.95, according to ZipRecruiter salary data. Most workers in this role earn between $21.92 and $30.58 per hour, depending on experience, location, and employer.

Is a Software QA Engineer Intern still in demand?

Software QA Engineer Intern positions remain in demand as companies continue to prioritize quality assurance in software development. Interns with skills in testing tools, scripting, and understanding of software development processes are sought after to support quality teams and gain industry experience.

What are the key skills and qualifications needed to thrive in the software QA engineer intern position, and why are they important?

To excel as a Software QA Engineer Intern, you should possess a foundation in computer science, basic understanding of software development and testing methodologies, and a keen attention to detail. Familiarity with test management tools (like JIRA or TestRail), version control systems (such as Git), and some exposure to automation frameworks (like Selenium) is often preferred. Effective communication, teamwork, and analytical thinking set standout candidates apart in this role. These skills are essential to ensure software quality, efficiently identify and resolve defects, and collaborate productively with development teams.

What are the typical responsibilities of a software QA engineer intern?

As a Software QA Engineer Intern, you’ll assist with writing and executing test cases, reporting software bugs, and collaborating with developers to troubleshoot and resolve issues. Your daily work may involve manual and automated testing, documenting results, and participating in agile team meetings. You’ll also learn about industry-standard testing tools and processes, gaining hands-on experience in quality assurance workflows. This role provides an excellent opportunity to build technical skills and understand the software development lifecycle, all while working alongside experienced QA professionals.

What is a software QA engineer intern?

A Software QA Engineer Intern assists in testing software applications to ensure they meet quality standards before release. They help design test cases, execute manual and automated tests, and document defects. Interns collaborate with developers and QA teams to identify and resolve issues, improving software reliability. This role provides hands-on experience with testing tools, methodologies, and industry best practices.

What are the most commonly searched types of Software Qa Engineer jobs in Portland, OR? The most popular types of Software Qa Engineer jobs in Portland, OR are:
What are popular job titles related to Software Qa Engineer Intern jobs in Portland, OR? For Software Qa Engineer Intern jobs in Portland, OR, the most frequently searched job titles are:
What cities near Portland, OR are hiring for Software Qa Engineer Intern jobs? Cities near Portland, OR with the most Software Qa Engineer Intern job openings:
Infographic showing various Software Qa Engineer Intern job openings in Portland, OR as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $56,065 per year, or $27 per hour.

Senior Quality Assurance Engineer

Genentech, Inc.

Hillsboro, OR • On-site

$93K - $172K/yr

Full-time

Re-posted 4 days ago


Genentech rating

8.8

Company rating: 8.8 out of 10

Based on 22 frontline employees who took The Breakroom Quiz

11th of 86 rated pharmaceutical


Job description

This role is a valuable part of our Hillsboro Innovative Therapies (HIT) Quality Systems and Validation team, which is committed to achieving our mission of delivering novel and exciting biopharmaceutical technologies to patients. As a member of this dedicated cross-functional team, you will drive production start-up activities and establish the foundational quality approach for new facilities. You will have the opportunity to collaborate closely with key stakeholders in Engineering, Operations, and global network teams to ensure our systems and processes are safe, compliant, and inspection-ready.
The Opportunity
As a Senior Quality Assurance Engineer, you will provide day-to-day Quality Oversight for site qualification, equipment validation, and computer system validation during critical production start-up activities. You will act as the site Quality and Regulatory Subject Matter Expert (SME), ensuring that all local processes and automated systems strictly align with current Good Manufacturing Practices (cGMPs). Key responsibilities include:
  • Lead Quality Oversight: Provide technical and regulatory oversight for site qualification and validation activities, including advanced Computer System Validation (CSV).
  • Approve Critical Validation: Review and approve essential lifecycle documentation such as Validation Master Plans, User Requirements, Protocols, deviations, and Summary Reports.
  • Support Engineering & Design: Collaborate during the build and deploy phases to support user requirement definitions and design specifications for production and laboratory equipment.
  • Defend Inspection Readiness: Maintain the compliance status of assigned areas to ensure a constant state of inspection readiness, and directly present and defend the validation program during regulatory audits.
  • Manage Risk & Changes: Provide technical quality assessments and approvals for engineering modifications, process changes, and Corrective and Preventive Actions (CAPAs) while managing the validation risk log.
  • Drive Continuous Improvement: Partner with interdepartmental, multi-site, and global corporate teams to implement validation best practices and benchmark against industry standards.

Who You Are
  • Education & Experience: Bachelor's degree (preferably in Engineering or Life Sciences) with a minimum of 8 years of pharmaceutical/biopharmaceutical industry experience, or a Master's degree with a minimum of 6 years of relevant industry experience. Cell therapy experience is preferred.
  • Validation & Engineering Expertise: Possess sound knowledge of engineering principles, qualification concepts, and regulatory requirements as they relate to system performance and laboratory design/start-up activities.
  • Automation & Systems Knowledge:Technical familiarity with the design, build, and deployment of automation and execution systems (such as Delta V/SCADA, Syncade MES, BAS, EBR, and Pi Data historian) within a regulated environment.
  • Regulatory & Risk Frameworks: Strong understanding of US and EU cGMPs, validation guidelines, and Risk Assessment Methodologies (such as PHA, FMEA, and FTA).
  • Decision-Making & Quality Analysis: Demonstrated ability to interpret complex Quality standards, make sound technical decisions, and troubleshoot cross-functional quality issues effectively.
  • Collaborative Communication: Excellent verbal and written communication skills with a proven track record of working collaboratively in cross-functional teams to achieve project milestones.
  • Physical & Travel Requirements:Ability to meet standard office physical demands (sitting/standing for extended periods, lifting up to 25 lbs) and a willingness to travel up to 30% to other sites as required.

The expected salary range for this position based on the primary location of Oregon is $93,000 - $172,800. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed in this link.
This is an on-site position.
Relocation benefits are not approved for this posting.

#LI-CA1
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Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.
If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.

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About Genentech

Sourced by ZipRecruiter

A member of the Roche Group, Genentech has been at the forefront of the biotechnology industry for more than 40 years, using human genetic information to develop novel medicines for serious and life-threatening diseases. Genentech has multiple therapies on the market for cancer & other serious illnesses. Please take this opportunity to learn about Genentech where we believe that our employees are our most important asset & are dedicated to remaining a great place to work.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

South San Francisco, CA, US

Year founded

1976

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