CPT Quality Assurance Associate Jobs
Quality Assurance Associate roles fit CPT when testing, auditing, or compliance work is directly tied to your enrolled coursework in engineering, computer science, or a related field. Your DSO must authorize each position before you start, so confirm the role description maps to your curriculum before accepting an offer.
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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 Associate CPT: Frequently Asked Questions
Does a Quality Assurance Associate role qualify for CPT authorization?
Yes, if the QA work is an integral part of your enrolled curriculum. Your DSO will look for a direct connection between your coursework, such as software engineering, industrial engineering, or systems analysis, and the duties in the offer letter. Roles focused on test case design, defect management, or process auditing typically satisfy that requirement when your major covers those competencies.
Can I do full-time CPT as a Quality Assurance Associate without losing OPT?
You can, but accumulating 12 or more months of full-time CPT eliminates your OPT eligibility entirely. Part-time CPT, which USCIS defines as fewer than 20 hours per week, does not count toward that limit regardless of total duration. If you need OPT for post-graduation employment or an H-1B visa transition, discuss the scheduling structure with your DSO before accepting a full-time CPT offer.
What documents does my employer need from me to hire me on CPT?
Your employer needs a valid I-20 with the CPT authorization printed on page two, showing the employer name, position title, start and end dates, and whether the authorization is part-time or full-time. They'll also run I-9 verification using those documents. Some employers, particularly government contractors, additionally require E-Verify completion before your first day, so confirm their onboarding checklist early.
How do I find Quality Assurance Associate jobs that are open to F-1 CPT students?
Migrate Mate filters Quality Assurance Associate openings by employers with documented work-authorization filing history, which helps you focus on companies that understand F-1 CPT rather than those encountering it for the first time. Narrowing your search to employers already familiar with authorization requirements reduces the back-and-forth during the offer stage and gives your DSO a cleaner paper trail to review.
Can my CPT be extended if the QA project runs longer than the original end date?
Yes, CPT can be extended, but your DSO must issue a new I-20 with an updated authorization before the original end date lapses. You'll typically need an updated offer letter or project scope from your employer confirming the extended timeline and continued academic relevance. Working past your authorized CPT end date without a new I-20 puts your F-1 status at risk, so request the extension at least two weeks before the deadline.