CPT Quality Assurance Associate Jobs
Quality Assurance Associate roles fit CPT when testing, auditing, or compliance work is directly tied to your enrolled coursework in engineering, computer science, or a related field. Your DSO must authorize each position before you start, so confirm the role description maps to your curriculum before accepting an offer.
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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 Associate CPT: Frequently Asked Questions
Does a Quality Assurance Associate role qualify for CPT authorization?
Yes, if the QA work is an integral part of your enrolled curriculum. Your DSO will look for a direct connection between your coursework, such as software engineering, industrial engineering, or systems analysis, and the duties in the offer letter. Roles focused on test case design, defect management, or process auditing typically satisfy that requirement when your major covers those competencies.
Can I do full-time CPT as a Quality Assurance Associate without losing OPT?
You can, but accumulating 12 or more months of full-time CPT eliminates your OPT eligibility entirely. Part-time CPT, which USCIS defines as fewer than 20 hours per week, does not count toward that limit regardless of total duration. If you need OPT for post-graduation employment or an H-1B visa transition, discuss the scheduling structure with your DSO before accepting a full-time CPT offer.
What documents does my employer need from me to hire me on CPT?
Your employer needs a valid I-20 with the CPT authorization printed on page two, showing the employer name, position title, start and end dates, and whether the authorization is part-time or full-time. They'll also run I-9 verification using those documents. Some employers, particularly government contractors, additionally require E-Verify completion before your first day, so confirm their onboarding checklist early.
How do I find Quality Assurance Associate jobs that are open to F-1 CPT students?
Migrate Mate filters Quality Assurance Associate openings by employers with documented work-authorization filing history, which helps you focus on companies that understand F-1 CPT rather than those encountering it for the first time. Narrowing your search to employers already familiar with authorization requirements reduces the back-and-forth during the offer stage and gives your DSO a cleaner paper trail to review.
Can my CPT be extended if the QA project runs longer than the original end date?
Yes, CPT can be extended, but your DSO must issue a new I-20 with an updated authorization before the original end date lapses. You'll typically need an updated offer letter or project scope from your employer confirming the extended timeline and continued academic relevance. Working past your authorized CPT end date without a new I-20 puts your F-1 status at risk, so request the extension at least two weeks before the deadline.