CPT Quality Assurance Inspector Jobs
Quality Assurance Inspector jobs involve hands-on inspection, testing, and process auditing that directly support coursework in manufacturing, industrial engineering, and supply chain management. CPT authorization requires your DSO to confirm the role is an integral part of your curriculum, so align your offer letter's job duties to your program requirements before requesting CPT.
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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 Inspector CPT: Frequently Asked Questions
Does a Quality Assurance Inspector role qualify for CPT authorization?
Yes, if your degree program includes coursework in quality management, manufacturing processes, industrial engineering, or a related field. Your DSO authorizes CPT only when the role is an integral part of your curriculum, so you'll need to show how inspection, process auditing, or testing duties connect directly to your enrolled courses. An offer letter listing specific job functions helps make that case.
Can I do CPT part-time as a QA Inspector while finishing my degree?
Yes. CPT can be part-time (under 20 hours per week) or full-time (20 hours or more). Part-time CPT is common for students completing final coursework while gaining practical experience. Full-time CPT is typically limited to specific circumstances such as thesis research or a required co-op term. Using 12 months or more of full-time CPT eliminates your OPT eligibility, so plan accordingly with your DSO.
What job duties should a QA Inspector CPT role include?
A qualifying CPT role should include duties like performing dimensional or visual inspection, documenting nonconformances, conducting process audits, applying statistical quality control methods, or working with ISO or AS9100 standards. These tasks map to industrial and manufacturing engineering curricula. Roles limited to administrative support or data entry under a QA title may not satisfy the integral curriculum requirement your DSO must verify.
Will working as a QA Inspector on CPT affect my future OPT or H-1B options?
Part-time CPT has no impact on OPT eligibility regardless of duration. Full-time CPT totaling 12 months or more eliminates standard OPT eligibility. For H-1B visa, Quality Assurance Inspector roles typically qualify as specialty occupations under engineering or quality management when the position requires at least a bachelor's degree in a related field. Choosing employers with prior H-1B filing history is a practical way to assess long-term sponsorship potential.
How do I find Quality Assurance Inspector jobs that accept CPT students?
Migrate Mate lets you filter for employers who hire F-1 students and have a history of supporting international candidates in technical roles. Focus on manufacturing, aerospace, medical device, and automotive employers, which regularly hire CPT students for quality and inspection positions. Verify that any employer you target can issue an offer letter with sufficient job-duty detail to satisfy your DSO's CPT authorization requirements.