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 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.
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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.