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Qa Automation Intern Jobs in Renton, WA (NOW HIRING)

AditiStaffing

Automation & Performance QA

Bellevue, WA · On-site

Company Description An IT Staffing Firm, established in 1994, headquartered in Bellevue, WA, with locations across the US. Technology is in our DNA - Aditi Staffing, an Aditi Technologies company ...

Apex Systems

Content QA Analyst

Redmond, WA · On-site

$33 - $37/hr

Bachelor's degree in Content Automation, Computer Science, Engineering, Information Systems, or a related field. Experience: 2-4 years of experience in QA, content testing, usability testing, or ...

Costco

Manager, Quality Assurance

Issaquah, WA · On-site

$160K - $180K/yr

Manager, Quality Assurance Manage, develop, and lead the design and implementation of functional ... Conduct automation of test suites review. Design test plans integrated with Selenium and Rest ...

Syntricate Technologies

SDET Level II

Seattle, WA · On-site

$57 - $73.50/hr

Required : • QA Automation • UI Testing • Javascript • Hardware Testing • IOT • 5+ years performing QA Automation at Sr Level • Strong UI focus on testing using React / Javascript • ...

Ampcus Inc

Quality Assurance Tech II

Seattle, WA · On-site

... Quality Assurance Tech II to join their talented team. The role involves testing software ... automation scripts. Responsibilities : • Create and run test plans, test cases, and test scripts ...

TekWissen LLC

Quality Assurance Tech II

Seattle, WA · On-site

Position: Quality Assurance Tech II Location: Seattle, WA 98109 Duration: 9 Months Job Type ... Mobile automation for Client's Payment products using Java, open source and Client's tools.

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All JobsQa Automation Intern JobsQa Automation Intern Jobs in Renton, WA

Qa Automation Intern information

See Renton, WA salary details

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How much do qa automation intern jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for qa automation intern in Renton, WA is $19.16, according to ZipRecruiter salary data. Most workers in this role earn between $16.20 and $21.63 per hour, depending on experience, location, and employer.

What does a QA Automation Intern do?

A QA Automation Intern assists with the development, execution, and maintenance of automated tests to ensure the quality of software applications. They work closely with QA engineers and developers to identify bugs, create test scripts, and help improve testing processes. Their responsibilities often include writing code for automated tests, running test cases, and documenting test results. This role provides valuable hands-on experience with software testing tools and methodologies, helping interns build essential skills for a career in quality assurance.

What types of projects can a QA Automation Intern expect to work on, and how are their tasks typically structured within the team?

As a QA Automation Intern, you can expect to work on tasks such as developing and maintaining automated test scripts, executing regression and functional tests, and assisting in identifying software defects. Interns often collaborate closely with experienced QA engineers and developers, participating in daily stand-up meetings and code reviews. Projects may include working with test frameworks like Selenium or Cypress and integrating test suites into CI/CD pipelines. The structure is usually supportive, offering mentorship and regular feedback to help you build technical skills and understand best practices in software quality assurance.

What are the key skills and qualifications needed to thrive as a QA Automation Intern, and why are they important?

To thrive as a QA Automation Intern, you need a solid understanding of software testing fundamentals, basic programming skills (often in languages like Python, Java, or JavaScript), and knowledge of the software development lifecycle. Familiarity with automation frameworks such as Selenium or Cypress, version control systems like Git, and basic knowledge of CI/CD tools are typically expected. Strong attention to detail, problem-solving abilities, and effective communication help interns excel in identifying and reporting issues. These skills are crucial for ensuring software quality, efficient testing processes, and effective collaboration within development teams.

What is the difference between Qa Automation Intern vs Qa Tester?

AspectQa Automation InternQa Tester
Required CredentialsTypically pursuing or recent graduate in Computer Science or related fieldOften has relevant certifications or experience in manual testing
Work EnvironmentInternship setting, learning-focused, entry-level tasksFull-time or part-time testing roles, may include manual and automated testing
Employer & Industry UsageUsed in tech companies, software firms, and startups for training and entry rolesCommon across software development companies, QA departments, and IT firms

The main difference is that a Qa Automation Intern is typically a student or recent graduate gaining experience in automation testing, while a Qa Tester may have more hands-on testing experience, including manual testing. Interns focus on learning and supporting automation tasks, whereas Qa Testers perform broader testing responsibilities.

Is QA automation intern a good entry-level job?

A QA automation intern role is generally considered a good entry-level position for those interested in software testing and automation. It provides hands-on experience with testing tools, scripting languages, and quality assurance processes, which can serve as a foundation for a career in software development or testing. However, the role typically requires basic knowledge of programming and testing concepts.

What job categories do people searching Qa Automation Intern jobs in Renton, WA look for?

The top searched job categories for Qa Automation Intern jobs in Renton, WA are:

What cities near Renton, WA are hiring for Qa Automation Intern jobs?

Cities near Renton, WA with the most Qa Automation Intern job openings:

Qa Automation Intern jobs near you
Infographic showing various Qa Automation Intern job openings in Renton, WA as of August 2026, with employment types broken down into 88% Full Time, 8% Part Time, and 4% Contract. Highlights an 81% Physical, 6% Hybrid, and 13% Remote job distribution, with an average salary of $39,859 per year, or $19.2 per hour.

Automation CSV Engineer - Site Based, Redmond, WA

Just - Evotec Biologics

Redmond, WA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 4 days ago

Job description

Job Title: Automation CSV Engineer
Location: Redmond, WA
Department: Global MSAT
About Us: this is who we are
At Evotec, we believe that curiosity is the spark that drives innovation and success. As a forward-thinking team, we thrive on challenging the status quo, learning from each other, and pushing the boundaries of what's possible. We're on a mission to create a place where curiosity isn't just encouraged-it's celebrated.
Are you someone who asks questions, seeks answers, and isn't afraid to go deeper? #BeCureious with us and see where your curiosity can take you!
The Role: / your challenge, ...in our journey
The Automation CSV Engineer is responsible for supporting validation, compliance, testing, and technical documentation activities for GMP automation systems within a regulated manufacturing environment. This role partners closely with Automation, Quality Assurance (QA), IT CSV, Manufacturing, and Engineering teams to help ensure automation systems remain compliant, reliable, and maintained in a validated state throughout the system lifecycle.
The ideal candidate will have experience supporting automation validation and Computer System Validation (CSV) activities for manufacturing systems such as DeltaV, PI, SCADA, PLC, and related automation platforms. This position requires strong technical writing skills, attention to detail, and the ability to collaborate effectively across cross-functional teams in support of GMP manufacturing operations.
What You'll Do:
Automation Validation & Compliance Support
  • Support validation and lifecycle management activities for GMP automation systems including DeltaV, PI, SCADA, PLC, and associated manufacturing control platforms.
  • Assist in ensuring automation systems remain compliant with GxP regulations, internal procedures, and industry standards throughout the system lifecycle.
  • Participate in implementation, upgrade, patching, migration, and change control activities for automation systems.
  • Support maintenance of the validated state for manufacturing automation systems and associated infrastructure.

Validation Documentation & Technical Writing
  • Author, revise, review, and maintain validation lifecycle documentation including: Validation Plans IQ/OQ/PQ Protocols Test Scripts Traceability Matrices Functional Specifications Discrepancy Reports Summary Reports SOPs and Work Instructions
  • Ensure validation documentation is accurate, complete, and aligned with internal quality standards and regulatory expectations.
  • Support document review and approval workflows within electronic quality management systems.

Testing & Execution Support
  • Execute and support commissioning, qualification, and validation testing activities including FAT, SAT, IQ, OQ, PQ, and automation functional testing.
  • Document test execution results, discrepancies, deviations, and corrective actions in accordance with approved procedures.
  • Coordinate testing activities with Automation, QA, ITCSV, Validation, and system owners to support project timelines and operational readiness.
  • Assist with troubleshooting issues identified during testing and support resolution activities.

Cross-Functional Collaboration
  • Serve as a liaison between QA, Automation, ITCSV, Engineering, and Manufacturing teams to support alignment of validation and compliance activities.
  • Collaborate with system owners and technical SMEs to gather system requirements and support risk assessments for automation systems.
  • Participate in project meetings, change control reviews, deviation investigations, and quality discussions related to automation systems.
  • Support vendor and integrator coordination activities as needed for system implementations and upgrades.

Risk-Based Validation & Quality Systems
  • Support risk-based validation approaches aligned with FDA CSA principles, GAMP 5 guidance, and Data Integrity expectations.
  • Assist in execution of Quality Risk Management (QRM) activities related to automation systems and computerized systems.
  • Support periodic reviews, audit readiness activities, and inspection support for validated automation systems.
  • Participate in continuous improvement initiatives focused on validation efficiency, documentation quality, and testing practices.

Automation System Support
  • Assist in reviewing automation system configurations, interfaces, alarms, security settings, and process control functionality for compliance and validation impact.
  • Support data integrity assessments, user access reviews, backup verification, and audit trail review activities where applicable.
  • Work with Automation and IT teams to support system reliability, compliance, and operational continuity.
  • Maintain awareness of current regulatory guidance and industry best practices related to CSV and automation validation.

Position Requirements
  • Bachelor's degree in Engineering, Computer Science, Biotechnology, Information Systems, or related technical discipline preferred.
  • Minimum of 5 years of experience supporting GMP automation systems, computer system validation (CSV), automation testing, or technical writing activities within regulated industries.
  • Hands-on experience with automation platforms such as DeltaV, PI, SCADA, PLC, or related manufacturing systems.
  • Experience executing validation and qualification activities including FAT, SAT, IQ, OQ, PQ, and functional testing.
  • Strong technical writing skills with experience authoring validation documentation and compliance records.
  • Working knowledge of GxP regulations and industry guidance including: 21 CFR Part 11 Annex 11 GAMP 5 FDA CSA principles Data Integrity requirements
  • Understanding of automation system lifecycle management and pharmaceutical quality systems.
  • Experience supporting change controls, deviations, CAPAs, and risk assessments within GMP environments.
  • Strong organizational skills and attention to detail with the ability to manage multiple assignments simultaneously.
  • Effective communication and collaboration skills with the ability to work across technical and business functions.

Preferred Qualifications
  • Experience supporting pharmaceutical, biotechnology, cell therapy, gene therapy, or medical device manufacturing operations.
  • Familiarity with MES, historians, batch systems, or manufacturing data systems.
  • Exposure to electronic quality management systems (eQMS), document management systems, and change management processes.
  • Experience supporting regulatory inspections or internal audits.
  • Understanding of SDLC methodologies and risk-based validation practices.
  • Knowledge of networking, system interfaces, or industrial automation infrastructure concepts.
  • Experience working with system integrators, vendors, or third-party validation providers.

Travel & Work Flexibility
  • Occasional travel to manufacturing or project sites may be required.
  • Flexibility in working hours may be needed during validation execution, project support activities, or manufacturing shutdown windows.

Why Join Us:
  • Growth Opportunities: We're a company that believes in continuous learning and development. Whether it's professional courses, mentorship, or new projects, we'll help you grow.
  • Flexible Work Environment: We offer flexible work options to help you balance your professional and personal life. Site based role.
  • Inclusive Culture: We're committed to building a diverse and inclusive environment where everyone's voice is valued, and curiosity is encouraged.
  • Innovative Projects: You'll have the chance to work on groundbreaking initiatives and cutting-edge technology in an atmosphere where your curiosity is the key to success.
  • A Place for Big Ideas: We don't just talk about thinking outside the box-we throw the box away. If you've got ideas, we want to hear them.

Are You Still Curious?
If you've read this far, then chances are you've got a curious mind-just like us. So, what are you waiting for? Take the leap and apply today. We can't wait to see where your curiosity leads you-and how it will shape the future of Evotec.
Let your curiosity guide your career-#BeCurious and explore the endless possibilities at Evotec!
The base pay range for this position at commencement of employment is expected to be $115,000 to $126,500; Base salary offered may vary depending on individual's skills, experience and competitive market value. Additional total rewards include discretionary annual bonus, comprehensive benefits to include Medical, Dental and Vision, short-term and long-term disability, company paid basic life insurance, 401k company match, flexible work, generous paid time off and paid holiday, wellness and transportation benefits.
Evotec (US) Inc. is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, gender, age, disability, genetic information, gender expression, gender identity, national origin, religion, sexual orientation, or veteran status.

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