Entry Level Software Quality Engineer Jobs
New grad software quality engineer jobs welcome recent graduates and entry level candidates with zero to two years of experience, where a strong portfolio or internship project can matter more than a long resume. Most openings are on-site and hybrid roles across Technology & Software, Medical Devices, and Construction & Real Estate, with employers like HP, Knapp, and XoriantːUS hiring at this level now.
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Software Quality Engineer I is a dual-purpose role that supports new deployments, sustaining, and/or optimization of the Manufacturing Execution System (MES) and the validation/sustainment of software that supports the quality system, manufacturing, distribution, and other GXP-related functions. This includes creating validation plans, reviewing and approval of software changes, and reviewing validation protocols/reports and developing requirements, revising/creating procedures, authoring MES and software validation/sustainment test cases, executing test cases and maintaining the integrity of the electronic device history record (eDHR).
Job Details:
- Develops software validation strategies for new and revised quality system and manufacturing software. Works with the team to provide appropriate guidance and support throughout the projects. Reviews and approves validations, test scripts, and reports.
- Supports the continuous improvement of TMC’s software validation and controls processes in accordance with regulatory requirements.
- Interprets and provides guidance on appropriate risk-based techniques for software validation and controls.
- Functions as an integrated MES team member to support new MES deployments, sustaining, and optimization projects.
- Assists with development of MES validation test cases and support Software Verification & Validation activities that include CRS revisions and test case execution.
- Supports the maintenance for the compliance of the MES system, the integrity of its validated state, and the eDHR.
Position Requirements:
- Knowledge of MES and its role in an organization.
- Knowledge of Computer Software Assurance (CSA) principles.
- Knowledge of ALCOA+ and Data Integrity principles.
- Effective communication (written and verbal).
- Ability to follow established procedures.
- Attention to detail and commitment to quality.
- Strong proofreading and writing skills.
- Strong organizational and prioritization skills.
- Ability to multitask, prioritize, and provide deliverables within the required time period.
- Strong computer knowledge (MS Office).
- Ability to work as a team member on cross-functional teams and with associates across all levels within the organization.
Background Experiences:
- Associate’s degree required in engineering or a scientific discipline or equivalent combination of education and experience.
- Minimum of 2 years relevant Computerized System Validation (CSV) or 1 year CSV and 1-year relevant Process Validation experience in the medical device/pharmaceutical industry.
- Experience with 21 CFR Part 11 and GAMP 5 computer system validation and control requirements.
- Experience with 21 CFR Part 820 and ISO 13485.
- Experience with manufacturing and quality system principles.
- Experience in medical device industry is preferred.
Benefits and Compensation:
We provide competitive and comprehensive benefit options that allow you to design your own plan based on your individual needs which include: paid vacation, paid holidays, health, dental and vision benefits, 401(k), with matching contributions, tax advantage savings accounts, legal plan, voluntary life and AD&D insurance, voluntary long-term disability, short term disability, critical illness and accident insurance, parental leave, personal leave, tuition reimbursement, travel assistance, and an employee assistance program. Salary range is $68,000 - $90,000 per year.
Employee Value Proposition:
We believe that the future is bright for everyone at Terumo. We work with the future in mind to generate lasting change, create a bigger impact and produce greater outcomes for today, and for decades to come. At Terumo we believe in the power of personal growth and will encourage you to get in the driver’s seat – progressing in the direction you want to go by deepening your skills throughout your career. We want you to be bold, think outside the box, experiment, innovate and deliver what’s next for quality healthcare. You will be part of a collaborative, respectful and resilient team of associates and leaders around the world, working together as partners to achieve more than you thought possible, providing real-world, sustainable solutions for patients.
Join us, and help shape wherever we go next!
Advancing healthcare with heart.
Job Summary
Software Quality Engineer I is a dual-purpose role that supports new deployments, sustaining, and/or optimization of the Manufacturing Execution System (MES) and the validation/sustainment of software that supports the quality system, manufacturing, distribution, and other GXP-related functions. This includes creating validation plans, reviewing and approval of software changes, and reviewing validation protocols/reports and developing requirements, revising/creating procedures, authoring MES and software validation/sustainment test cases, executing test cases and maintaining the integrity of the electronic device history record (eDHR).
Job Details:
- Develops software validation strategies for new and revised quality system and manufacturing software. Works with the team to provide appropriate guidance and support throughout the projects. Reviews and approves validations, test scripts, and reports.
- Supports the continuous improvement of TMC’s software validation and controls processes in accordance with regulatory requirements.
- Interprets and provides guidance on appropriate risk-based techniques for software validation and controls.
- Functions as an integrated MES team member to support new MES deployments, sustaining, and optimization projects.
- Assists with development of MES validation test cases and support Software Verification & Validation activities that include CRS revisions and test case execution.
- Supports the maintenance for the compliance of the MES system, the integrity of its validated state, and the eDHR.
Position Requirements:
- Knowledge of MES and its role in an organization.
- Knowledge of Computer Software Assurance (CSA) principles.
- Knowledge of ALCOA+ and Data Integrity principles.
- Effective communication (written and verbal).
- Ability to follow established procedures.
- Attention to detail and commitment to quality.
- Strong proofreading and writing skills.
- Strong organizational and prioritization skills.
- Ability to multitask, prioritize, and provide deliverables within the required time period.
- Strong computer knowledge (MS Office).
- Ability to work as a team member on cross-functional teams and with associates across all levels within the organization.
Background Experiences:
- Associate’s degree required in engineering or a scientific discipline or equivalent combination of education and experience.
- Minimum of 2 years relevant Computerized System Validation (CSV) or 1 year CSV and 1-year relevant Process Validation experience in the medical device/pharmaceutical industry.
- Experience with 21 CFR Part 11 and GAMP 5 computer system validation and control requirements.
- Experience with 21 CFR Part 820 and ISO 13485.
- Experience with manufacturing and quality system principles.
- Experience in medical device industry is preferred.
Benefits and Compensation:
We provide competitive and comprehensive benefit options that allow you to design your own plan based on your individual needs which include: paid vacation, paid holidays, health, dental and vision benefits, 401(k), with matching contributions, tax advantage savings accounts, legal plan, voluntary life and AD&D insurance, voluntary long-term disability, short term disability, critical illness and accident insurance, parental leave, personal leave, tuition reimbursement, travel assistance, and an employee assistance program. Salary range is $68,000 - $90,000 per year.
Employee Value Proposition:
We believe that the future is bright for everyone at Terumo. We work with the future in mind to generate lasting change, create a bigger impact and produce greater outcomes for today, and for decades to come. At Terumo we believe in the power of personal growth and will encourage you to get in the driver’s seat – progressing in the direction you want to go by deepening your skills throughout your career. We want you to be bold, think outside the box, experiment, innovate and deliver what’s next for quality healthcare. You will be part of a collaborative, respectful and resilient team of associates and leaders around the world, working together as partners to achieve more than you thought possible, providing real-world, sustainable solutions for patients.
Join us, and help shape wherever we go next!
Advancing healthcare with heart.
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Entry Level Software Quality Engineer Jobs: Frequently Asked Questions
How do I get an entry level software quality engineer job?
Focus on building hands-on experience through internships, capstone projects, or personal test automation work you can show on GitHub. Employers hiring at this level look for familiarity with tools like Selenium, JIRA, or Postman, a basic understanding of the software development lifecycle, and the ability to write clear bug reports. Certifications such as ISTQB Foundation can help a new grad stand out.
Which companies hire entry level software quality engineers?
Companies hiring entry level software quality engineers right now include HP, Knapp, and XoriantːUS, based on current listings on Migrate Mate as of November 2026. At this level, you will find openings at a mix of large technology companies, financial services firms, healthcare technology providers, and mid-size software product companies that run dedicated QA teams.
Are there remote entry level software quality engineer jobs?
Yes, though many entry level roles still prefer on-site or hybrid arrangements to support onboarding. About 33% of entry level software quality engineer openings are remote or hybrid as of November 2026, so candidates who need location flexibility will find options, particularly at larger technology employers and software-as-a-service companies.
Are these new grad software quality engineer jobs?
Yes, the listings on this page include new grad, recent graduate, and junior software quality engineer roles. A posting is typically new grad friendly when it welcomes zero to two years of experience, counts internships or co-op work toward that requirement, or explicitly accepts a strong portfolio in place of full-time work history. Look for phrases like 'entry level,' 'new grad,' or 'junior QA' in the job description.
Which industries hire the most entry level software quality engineers?
Entry Level software quality engineer roles concentrate in Technology & Software, Medical Devices, and Construction & Real Estate, based on current listings on Migrate Mate as of November 2026. These sectors drive hiring at this level because they ship software continuously and rely on structured QA pipelines, creating steady demand for junior testers who can grow into automation and performance engineering roles.