CPT QA Engineer Jobs
QA Engineer roles qualify for CPT when the work is directly tied to your degree program in computer science, software engineering, or a related field. Your DSO must authorize each position before you start. Roles involving test automation, defect tracking, and software validation align closely with technical degree curricula and typically meet CPT's integral-part requirement.
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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 JobsQA Engineer CPT: Frequently Asked Questions
Does a QA Engineer role qualify for CPT?
Yes, if the work is an integral part of your degree program and your school offers a course or practicum tied to it. Roles involving software testing, test automation, defect management, or quality assurance processes align well with computer science, software engineering, and information systems curricula. Your DSO makes the final determination based on your specific program requirements and the employer's job description.
Can I work as a QA Engineer on CPT before completing my first year of F-1 study?
No. F-1 students must complete one full academic year before becoming eligible for CPT. This is a USCIS requirement, not a school policy, so no DSO can waive it. If you receive a QA Engineer offer before your first year ends, the earliest your CPT authorization can begin is the first day after your one-year mark.
What documents does a QA Engineer CPT employer need from me?
Your employer needs your updated I-20 showing the CPT authorization on page two, with the correct employer name, start date, and end date listed. They also need your passport, F-1 visa stamp, and I-94 arrival record for I-9 verification. Some employers with E-Verify accounts will run your documents through the system on day one, which is standard practice and not a problem for F-1 CPT workers.
How do I find QA Engineer employers that understand F-1 CPT?
Search for employers with existing DOL Labor Condition Application filings for software quality or testing roles on Migrate Mate. Companies that have already navigated work authorization paperwork are significantly less likely to rescind offers when you present your CPT I-20. Avoid applying to employers advertising that they cannot provide any immigration support, as even CPT requires basic I-9 familiarity from the hiring team.
Does QA Engineer CPT count toward STEM OPT eligibility?
CPT itself doesn't directly qualify you for STEM OPT, but your degree does. If you graduate with a STEM-designated degree and your QA Engineer role falls under an eligible SOC code, such as Software Quality Assurance Analysts and Testers, you can apply for the 24-month STEM OPT extension after your initial 12-month OPT period. Confirm your program's STEM designation with your DSO before graduation.