CPT Quality Assurance Intern Jobs
Quality Assurance Intern roles in testing, compliance, and product validation are among the most CPT-compatible positions for F-1 students in engineering and computer science programs. Your DSO must authorize each CPT position individually, and the work must directly fulfill a curricular requirement, not just relate loosely to your field of study.
Find CPT Quality Assurance Intern JobsOverview
Showing 5 of 12+ Quality Assurance Intern jobs
See all Quality Assurance Intern Jobs
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Quality Assurance Intern roles.
Get Access To All JobsABOUT THE ORGANIZATION
SIMTEC is a leading, U.S.-based Extraordinary Solutions provider exclusively focused on the customized, serial production of Liquid Silicone Rubber (LSR), LSR over-molded and 2-Shot (LSR/Thermoplastic) solutions, and Multi-Shot (LSR/Thermoplastic and Metal) injection molded components. As a technology driven company, since 2002, SIMTEC has been envisioning and manufacturing high precision, tight tolerance solutions for global innovative leaders in the automotive, life science, electronic, infant and personal care industries. SIMTEC Silicone Parts is ISO 9001, ISO 13485, and ISO/TS 16949 certified, as well as cGMP compliant. The company is a proud member of the RICO GROUP.
Position Summary
To successfully perform this job, the individual must be able to perform each essential job responsibility satisfactorily. Reasonable accommodation may be made to enable an individual with disabilities to perform the essential job responsibilities. Job descriptions represent a general outline of job responsibilities and qualifications. They are not intended to be comprehensive in nature. In addition, jobs evolve over time and, therefore, their descriptions may not reflect the precise nature of the position at a given point of time.
GENERAL DESCRIPTION
The intern will assist with rebuilding and organizing critical quality and operational documentation following a cybersecurity recovery initiative. This role offers valuable exposure to document control systems, quality management processes, and cross-functional collaboration within a manufacturing environment.
ESSENTIAL JOB RESPONSIBILITIES:
- Analyze, improve, and standardize quality system documentation to support compliance with ISO 9001 and ISO 13485 requirements.
- Support document control activities within the Quality Management System (QMS).
- Assist with maintaining accurate records and revision controls.
- Help standardize file structures and document naming conventions.
- Support validation documentation activities.
- Collaborate with Engineering, Quality, and Production teams on documentation updates.
- Assist in ensuring compliance with internal procedures and customer requirements.
LOCATION
Location: Simtec
SALARY
EOE STATEMENT
We are an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status or any other characteristic protected by law.
This position is currently accepting applications.
ABOUT THE ORGANIZATION
SIMTEC is a leading, U.S.-based Extraordinary Solutions provider exclusively focused on the customized, serial production of Liquid Silicone Rubber (LSR), LSR over-molded and 2-Shot (LSR/Thermoplastic) solutions, and Multi-Shot (LSR/Thermoplastic and Metal) injection molded components. As a technology driven company, since 2002, SIMTEC has been envisioning and manufacturing high precision, tight tolerance solutions for global innovative leaders in the automotive, life science, electronic, infant and personal care industries. SIMTEC Silicone Parts is ISO 9001, ISO 13485, and ISO/TS 16949 certified, as well as cGMP compliant. The company is a proud member of the RICO GROUP.
Position Summary
To successfully perform this job, the individual must be able to perform each essential job responsibility satisfactorily. Reasonable accommodation may be made to enable an individual with disabilities to perform the essential job responsibilities. Job descriptions represent a general outline of job responsibilities and qualifications. They are not intended to be comprehensive in nature. In addition, jobs evolve over time and, therefore, their descriptions may not reflect the precise nature of the position at a given point of time.
GENERAL DESCRIPTION
The intern will assist with rebuilding and organizing critical quality and operational documentation following a cybersecurity recovery initiative. This role offers valuable exposure to document control systems, quality management processes, and cross-functional collaboration within a manufacturing environment.
ESSENTIAL JOB RESPONSIBILITIES:
- Analyze, improve, and standardize quality system documentation to support compliance with ISO 9001 and ISO 13485 requirements.
- Support document control activities within the Quality Management System (QMS).
- Assist with maintaining accurate records and revision controls.
- Help standardize file structures and document naming conventions.
- Support validation documentation activities.
- Collaborate with Engineering, Quality, and Production teams on documentation updates.
- Assist in ensuring compliance with internal procedures and customer requirements.
LOCATION
Location: Simtec
SALARY
EOE STATEMENT
We are an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status or any other characteristic protected by law.
This position is currently accepting applications.
See all CPT Quality Assurance Intern Jobs
Sign up for free to unlock all listings, filter by visa type, and get alerts for new CPT Quality Assurance Intern Jobs.
Get Access To All JobsQuality Assurance Intern CPT: Frequently Asked Questions
Does a Quality Assurance Intern role qualify for CPT?
Yes, as long as the QA work is an integral part of your curriculum and your DSO authorizes it. Programs in computer science, information systems, industrial engineering, and software engineering commonly include QA internships as fulfilling a practicum or project-based requirement. Your offer letter description should reference testing, validation, or quality processes that align with your program's learning objectives.
Can I do CPT for a QA internship at a startup or small company?
Yes. CPT eligibility depends on your school's authorization and the curricular connection, not the employer's size or industry. Small companies and startups don't need to file any paperwork with USCIS for CPT. The only requirement is that your DSO approves the specific position and employer, and that the work directly relates to your program of study.
How do I find Quality Assurance Intern roles that are open to F-1 CPT students?
Many QA internship postings don't specify CPT eligibility, so filtering by authorization type is more efficient than reading individual job descriptions. Migrate Mate surfaces roles where employers have a verified history of hiring F-1 students, letting you focus applications on companies already familiar with CPT documentation and I-20 requirements.
Does 12 months of full-time CPT in a QA role affect my OPT?
Yes, and this is one of the most consequential CPT rules for interns doing extended programs. USCIS considers 12 or more months of full-time CPT to eliminate your OPT eligibility entirely. Part-time CPT, defined as 20 hours per week or fewer, doesn't count toward that limit regardless of how many semesters it spans.
What documents does an employer need from me to hire me on CPT for a QA internship?
The employer needs your current I-20 with CPT authorization on page two, showing the specific employer name, job title, and authorized dates. They'll also need your F-1 visa and passport for Form I-9 verification. Unlike OPT, there's no EAD card for CPT. Your I-20 is the only work authorization document the employer needs to retain.