CPT Quality Assurance Analyst Jobs
Quality Assurance Analyst CPT jobs let F-1 students apply software testing, defect tracking, and process validation skills in a paid role that counts toward your degree. Your DSO must authorize CPT before your start date, and the work must connect directly to your program of study.
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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 Analyst CPT: Frequently Asked Questions
Does a Quality Assurance Analyst role qualify for CPT authorization?
Yes, if the work directly relates to your field of study. QA Analyst duties like test planning, defect analysis, and process documentation connect clearly to degrees in computer science, information systems, or software engineering. Your DSO makes the final determination, so bring a detailed job description that maps specific duties to courses in your program.
Can I do CPT as a Quality Assurance Analyst while attending school full time?
Part-time CPT, defined as 20 hours or fewer per week, doesn't affect your full-time enrollment requirement. Full-time CPT, more than 20 hours per week, is permitted but eliminates one semester of OPT eligibility for every 12 months used. Most F-1 students in QA roles choose part-time CPT during the academic year to protect their OPT.
How do I find Quality Assurance Analyst employers who hire CPT students?
Migrate Mate lets you filter QA Analyst openings by employers with a track record of hiring F-1 students and filing Labor Condition Applications for technical roles. Focusing on companies with existing LCA filings in software quality or systems testing reduces the time spent explaining your work authorization status to HR teams unfamiliar with CPT.
What documents do I need to start a CPT Quality Assurance Analyst job?
You need an updated I-20 with CPT authorization endorsed by your DSO, issued before your start date. You'll also need the employer's offer letter specifying your role title, start and end dates, weekly hours, and work location. Remote or hybrid QA roles must list the employer's physical address, not your home address, as the work site on your I-20.
Does CPT experience as a QA Analyst count toward H-1B specialty occupation requirements?
CPT work experience in a QA Analyst role is counted the same as any other professional work experience by USCIS. If your employer later files an H-1B visa petition for you, they'll reference your QA duties to demonstrate the role meets specialty occupation standards, typically a position requiring at least a bachelor's degree in a directly related technical field.