CPT Software QA Engineer Jobs
Software QA Engineer CPT positions let F-1 students apply testing frameworks, bug tracking, and quality assurance workflows directly tied to their degree program. Your DSO must authorize each position before you start, and the role must be listed on your I-20. Part-time CPT runs up to 20 hours per week during the semester; full-time is permitted during breaks.
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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 JobsSoftware QA Engineer CPT: Frequently Asked Questions
Does a Software QA Engineer role qualify for CPT authorization?
Yes, if the position directly relates to your degree program and your DSO agrees the work is an integral part of your curriculum. Degrees in computer science, software engineering, information systems, and related fields typically satisfy this standard for QA roles. Your school sets the final standard, so submit your offer letter and a written curriculum-connection statement to your DSO before accepting.
Can I do part-time CPT as a Software QA Engineer while taking classes?
Part-time CPT allows up to 20 hours per week during an active academic semester without affecting your OPT eligibility. Many QA employers offer structured part-time arrangements specifically for students, particularly for test automation, regression cycles, or sprint-based work that fits around a class schedule. Confirm the exact weekly hours in your offer letter so your I-20 reflects the correct authorization.
Will full-time CPT as a Software QA Engineer affect my OPT eligibility?
One year or more of full-time CPT eliminates your OPT eligibility entirely, per USCIS regulations. Part-time CPT, regardless of how many semesters you use it, does not count against OPT. If you're weighing a full-time QA internship against preserving OPT for post-graduation work, map out your total authorized full-time CPT months before committing to an extended engagement.
What documentation does a QA employer need to support my CPT authorization?
Most schools require a signed offer letter on company letterhead, the supervisor's contact information, and confirmation that the position is paid or for academic credit. Some DSOs also request a brief job description connecting QA tasks to your coursework. Prepare this packet before your first day because CPT authorization must be in place on your I-20 before you begin working, not retroactively.
How do I find Software QA Engineer jobs that are compatible with CPT?
Search Migrate Mate for Software QA Engineer roles and filter by employers with documented work-authorization experience. Employers who have previously filed for international employees are more likely to understand CPT documentation requirements and less likely to withdraw an offer when your DSO's authorization process takes time. Prioritize companies that list E-Verify enrollment, since that signals readiness for future OPT and STEM OPT transitions as well.