CPT Compliance Associate Jobs
Compliance Associate roles sit at the intersection of regulatory analysis, risk monitoring, and policy interpretation, all skills developed in law, finance, and business programs that qualify for CPT. Your DSO must authorize CPT before your start date, and the work must directly fulfill a curricular requirement, not run alongside it.
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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 JobsCompliance Associate CPT: Frequently Asked Questions
Does a Compliance Associate role qualify for CPT authorization?
Compliance Associate work generally qualifies for CPT when your program covers regulatory frameworks, risk management, or legal compliance as core curriculum topics. Your DSO makes the final determination based on how well the specific job duties map to your coursework. Roles in financial services, healthcare, or corporate governance compliance tend to align most directly with business, law, and public policy programs.
Can I do CPT at a financial services firm that requires a background check?
Yes. Background checks are a standard employer requirement and have no bearing on your CPT authorization. Your F-1 status and the CPT work authorization are issued by your school through USCIS-governed regulations, not by the employer. Complete the employer's screening process as any other candidate would. Just ensure your CPT is authorized and your I-20 is updated before your first day.
What happens if my Compliance Associate CPT ends before the project wraps up?
CPT is authorized for a specific period tied to your academic term. Working beyond your authorized end date violates your F-1 status, even if the employer wants you to continue. You'll need to request a new CPT authorization for the following term from your DSO before the prior period expires. Build a buffer into your timeline and communicate renewal requirements to your employer early.
How do I find Compliance Associate roles where employers are already familiar with CPT?
Search Migrate Mate for Compliance Associate openings filtered by employers with documented work authorization experience. Employers who have hired international students before understand CPT documentation requirements and are far less likely to rescind offers due to unfamiliarity with the process. Targeting these employers reduces friction at the offer and onboarding stage.
Will my Compliance Associate CPT experience count toward future H-1B specialty occupation evidence?
CPT work experience in compliance can strengthen a future H-1B visa petition by demonstrating that your role consistently required your specialized degree. Compliance Associate positions that involve regulatory interpretation, risk assessment, or policy analysis are more defensible as specialty occupations than general administrative compliance tasks. Document your responsibilities in detail throughout your CPT engagement for use in future filings.