CPT Quality Assurance Tester Jobs
Quality Assurance Tester roles align closely with computer science, software engineering, and information systems curricula, making them a strong CPT fit. Your DSO must authorize each position before you start, and the work must connect directly to your degree program. Part-time CPT during the semester and full-time CPT during breaks are both available options.
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Get Access To All JobsABOUT GENSCRIPT
GenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.
GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology.
2026 SUMMER INTERNSHIP
Genscript USA Inc. will support a Summer Internship Program that provides growth and learning opportunities to students currently pursuing an Undergrad/ Post-Grad degree.
Interns will be involved in a cohort training program designed to provide students with professional experience in the furtherance of their education. Internships assist students in reaching their educational goals by giving them the opportunity to augment classroom instruction with exposure to real world employment settings.
Overview:
Genscript is currently hiring for a Summer QA Intern to join our Quality Assurance team in Redmond reporting into the group Supervisor. This internship will be based in Redmond, WA and the hourly pay-rate is estimated at $20 - $25 per hour.
This intern will assist GenScript QA team members with day to day tasks. Working on a wide range of Quality related Compliance, Research, and administrative tasks.
Responsibilities:
- Review controlled and executed documentation to support checks for good documentation practices and compliance against Document Control procedures
- Review SOPs and affiliated forms to support assessments/opportunities for improvements
- Support document processing (operations) to ensure timely relay of document creation/revision requests
- Assist in training program documentation reconciliation reviews
- Assist in raw materials management documentation reconciliation
- Assist in internal audit preparations
- Assist in data analysis to identify trends and process improvement opportunities
- Assist in other QA related tasks
QUALIFICATIONS
- Currently enrolled in Bachelor's (Senior Status), Master's Program (any status), or recent graduate (within the last year)
- Communication skills (able to say when they have any confusion or have questions; willing to ask for help and/or escalate when there is a problem)
- Able to jump from task to task
- Willing to take on repetitive work
- A strong sense of responsibility and a proactive work attitude
- Effective time management and organizational skills
- Good communication skills, organized, responsible
GenScript USA Inc/ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law.
GenScript USA Inc./ProBio Inc. maintains a drug-free workplace.
Please note: Genscript USA Inc./ProBio Inc. will only contact candidates through verified application sources. GenScript/Probio does not request personal information from candidates through individual email or any other platform.
ABOUT GENSCRIPT
GenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.
GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology.
2026 SUMMER INTERNSHIP
Genscript USA Inc. will support a Summer Internship Program that provides growth and learning opportunities to students currently pursuing an Undergrad/ Post-Grad degree.
Interns will be involved in a cohort training program designed to provide students with professional experience in the furtherance of their education. Internships assist students in reaching their educational goals by giving them the opportunity to augment classroom instruction with exposure to real world employment settings.
Overview:
Genscript is currently hiring for a Summer QA Intern to join our Quality Assurance team in Redmond reporting into the group Supervisor. This internship will be based in Redmond, WA and the hourly pay-rate is estimated at $20 - $25 per hour.
This intern will assist GenScript QA team members with day to day tasks. Working on a wide range of Quality related Compliance, Research, and administrative tasks.
Responsibilities:
- Review controlled and executed documentation to support checks for good documentation practices and compliance against Document Control procedures
- Review SOPs and affiliated forms to support assessments/opportunities for improvements
- Support document processing (operations) to ensure timely relay of document creation/revision requests
- Assist in training program documentation reconciliation reviews
- Assist in raw materials management documentation reconciliation
- Assist in internal audit preparations
- Assist in data analysis to identify trends and process improvement opportunities
- Assist in other QA related tasks
QUALIFICATIONS
- Currently enrolled in Bachelor's (Senior Status), Master's Program (any status), or recent graduate (within the last year)
- Communication skills (able to say when they have any confusion or have questions; willing to ask for help and/or escalate when there is a problem)
- Able to jump from task to task
- Willing to take on repetitive work
- A strong sense of responsibility and a proactive work attitude
- Effective time management and organizational skills
- Good communication skills, organized, responsible
GenScript USA Inc/ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law.
GenScript USA Inc./ProBio Inc. maintains a drug-free workplace.
Please note: Genscript USA Inc./ProBio Inc. will only contact candidates through verified application sources. GenScript/Probio does not request personal information from candidates through individual email or any other platform.
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Get Access To All JobsQuality Assurance Tester CPT: Frequently Asked Questions
Does a Quality Assurance Tester role qualify for CPT authorization?
Yes, if the role connects directly to your degree program. QA Tester positions typically align with computer science, software engineering, information systems, or related majors. Your DSO evaluates whether the specific job duties, not just the title, are an integral part of your curriculum. Bring the job description to your DSO appointment so they can make that determination before you accept the offer.
Can I do CPT as a part-time QA Tester while classes are in session?
Yes. Part-time CPT, defined as 20 hours per week or fewer, does not affect your OPT eligibility regardless of how many semesters you use it. Full-time CPT, meaning more than 20 hours per week, used for 12 months or more eliminates your OPT eligibility entirely. Most F-1 students working QA roles during the academic semester keep hours at or below 20 to protect their post-graduation options.
What documents do I need to start a CPT-authorized QA Tester job?
You need a CPT-endorsed I-20 from your DSO showing your employer's name, the authorized employment dates, and whether the authorization is part-time or full-time. Your employer also needs your I-20 and EAD equivalent documentation for their I-9 and E-Verify records. Confirm with your employer's HR team which documents they require before your first day, since some companies request additional proof of enrollment.
How do I find QA Tester employers who are open to CPT students?
Search on Migrate Mate, which filters Quality Assurance Tester roles by employers with documented work-authorization filing history. Companies that have previously sponsored work visas are significantly more familiar with CPT paperwork and I-9 compliance than those who haven't. Targeting that subset of employers reduces the risk of losing an offer because HR doesn't know how to process your I-20 authorization.
Does CPT experience as a QA Tester count toward H-1B specialty occupation eligibility?
CPT work experience in QA testing can support an H-1B visa petition if the role required and you performed work requiring at least a bachelor's degree in a directly related field. USCIS evaluates the nature of the duties, not the CPT label. Keep detailed records of your QA projects, tools used, and the technical complexity of your work. That documentation strengthens a future employer's specialty occupation argument to USCIS.