CPT Quality Assurance Auditor Jobs
Quality Assurance Auditor roles in manufacturing, pharma, and regulated industries often involve structured compliance workflows that align directly with degree programs in industrial engineering, chemistry, or supply chain management, making them strong CPT fits. Your DSO will need to document how the auditing work integrates with your coursework before authorizing CPT.
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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 Auditor CPT: Frequently Asked Questions
Does a Quality Assurance Auditor role qualify for CPT authorization?
It depends on how directly the auditing duties connect to your enrolled coursework. Roles involving internal audits, process documentation, or regulatory compliance reviews typically qualify for students in industrial engineering, chemistry, supply chain, or business quality management programs. Your DSO makes the final determination, so bring the full job description and a written explanation of how each duty ties to a specific course.
Can I do CPT at a company that uses contractors or staffing agencies for QA roles?
Yes, but the CPT authorization must name the actual worksite employer, not the staffing agency. If a pharma company is the end client and the agency places you there, your I-20 must reflect the worksite employer's address and role details. Confirm this with your DSO before signing any staffing agreement, because mismatched employer information on your I-20 creates compliance problems.
How do I find Quality Assurance Auditor jobs that are open to CPT students?
Browse Quality Assurance Auditor listings on Migrate Mate, which filters for employers with F-1 CPT hiring experience. Regulated industries, medical devices, pharmaceuticals, food manufacturing, aerospace, are the most reliable sectors because their compliance obligations mean their HR teams already understand work authorization documentation requirements for international students.
What happens to my CPT authorization if my audit role shifts to a different department mid-internship?
Any material change to your duties, worksite location, or employer requires a new CPT authorization and an updated I-20. A lateral shift within the same QA function at the same worksite is usually fine without changes, but a move from product auditing to supplier auditing at an off-site facility is a different matter. Report the change to your DSO promptly rather than waiting until your semester check-in.
Does using CPT for a Quality Assurance Auditor role affect my future OPT eligibility?
Full-time CPT used for 12 months or more at any point during your program eliminates your OPT eligibility entirely. Part-time CPT, or full-time CPT totaling less than 12 months, does not affect OPT. Track your cumulative full-time CPT days carefully if you plan to use OPT after graduation, especially if you've held multiple CPT positions across different semesters.