CPT QA Analyst Jobs
QA Analyst roles sit squarely within computer science, information systems, and software engineering curricula, making them a strong CPT fit when your DSO confirms the work directly advances your degree requirements. Your authorization is tied to your current program, so the role's testing, debugging, and quality assurance duties need to map to your coursework.
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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 Analyst CPT: Frequently Asked Questions
Does a QA Analyst role qualify for CPT?
It depends on your degree program. CPT is authorized when the work is an integral part of your curriculum, so a QA Analyst role qualifies if your program includes coursework in software testing, systems engineering, or quality assurance methods. Your DSO makes the final determination based on your course of study, not the job title alone.
Can I do CPT as a QA Analyst while taking classes?
Yes, part-time CPT runs alongside your enrolled coursework. Most QA Analyst CPT authorizations are structured as part-time placements during the academic semester, with full-time CPT available during summer or winter breaks. Confirm the exact terms with your DSO, since each authorization is semester-specific and tied to your enrollment status.
How does CPT affect my OPT eligibility for future QA roles?
Twelve or more months of full-time CPT eliminates your post-completion OPT eligibility. Part-time CPT doesn't count against OPT regardless of duration. If you plan to use OPT to bridge into H-1B visa sponsorship after graduation, structure your QA Analyst CPT as part-time or keep full-time CPT under the 12-month threshold.
What documents does my employer need to start my CPT?
Your employer doesn't file anything with USCIS for CPT. The authorization happens entirely through your school. You'll need a written offer letter specifying the job title, employer name, work location, start and end dates, and weekly hours. Bring that to your DSO, who issues a new I-20 with CPT authorization. Your employer will need that updated I-20 for I-9 verification.
Where can I find QA Analyst jobs that are open to CPT students?
Migrate Mate lists QA Analyst roles from employers with documented experience hiring international students on CPT and OPT. Many tech companies, software consultancies, and enterprise IT teams hire QA interns and analysts on CPT regularly. Filtering for employers with prior international student hiring history saves significant time compared to applying broadly and screening manually.