CPT Quality Technician Jobs
Quality Technician jobs fit CPT because the hands-on inspection, measurement, and process-control work directly maps to coursework in engineering technology, manufacturing systems, or industrial quality programs. Your DSO must authorize each CPT position individually, and the role description should reference your specific degree program to satisfy that 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 JobsQuality Technician CPT: Frequently Asked Questions
Does a Quality Technician role qualify for CPT authorization?
Yes, if the role is an integral part of your curriculum. Quality Technician duties, such as dimensional inspection, calibration, and statistical process control, align closely with engineering technology, industrial technology, and manufacturing engineering programs. Your DSO will require a job offer letter and may ask you to document which specific courses the work experience satisfies before adding CPT to your I-20.
Can I do CPT at a manufacturing company that has never hired an F-1 student?
You can, but you'll need to walk the employer through the process. The employer's main obligation is completing Form I-9 correctly using your CPT-endorsed I-20 as a List A document. They don't file anything with USCIS. Confirm that HR understands CPT work authorization before your start date so there are no I-9 compliance issues on day one.
How do I find Quality Technician employers who are already set up for F-1 students?
Search Quality Technician openings on Migrate Mate, which filters for employers with documented work-authorization filing history. Employers who have previously hired F-1 students on OPT or sponsored H-1B visas already have I-9 and onboarding processes in place, which makes the CPT paperwork conversation much smoother than starting cold with an employer who has never done it.
What happens to my OPT if I do full-time CPT as a Quality Technician co-op?
Every month of full-time CPT, defined as more than 20 hours per week, counts against your 12-month OPT limit. A six-month full-time co-op leaves you with six months of post-completion OPT. Part-time CPT, at 20 hours or fewer per week, does not affect OPT eligibility at all. Confirm the weekly hours in your offer letter with your DSO before accepting.
Can a Quality Technician CPT role lead to H-1B sponsorship after graduation?
CPT itself doesn't obligate an employer to sponsor you later, but it can create that path. Quality Technician roles are typically classified as technical occupations under SOC codes tied to manufacturing or quality engineering, which can support an H-1B petition if the position requires a bachelor's degree in a relevant field. Employers in aerospace, automotive, and medical device manufacturing have consistent H-1B filing histories in these occupation categories.