CPT Compliance Specialist Jobs
Compliance Specialist jobs align with CPT when your program covers regulatory frameworks, risk management, or corporate governance. Your DSO must confirm the role is an integral part of your curriculum before you start. Roles in financial services, healthcare, and tech compliance are common CPT placements for business, law, and public policy students.
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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 Specialist CPT: Frequently Asked Questions
Does a Compliance Specialist role qualify for CPT authorization?
Yes, if your degree program includes coursework in regulatory compliance, business law, risk management, or corporate governance. Your DSO evaluates whether the specific job duties, not just the job title, are an integral part of your curriculum. Roles involving policy analysis, internal audits, or regulatory reporting are the easiest to tie to academic requirements.
Can I do CPT as a Compliance Specialist at a company that doesn't typically sponsor visas?
CPT authorization comes from your school, not the employer. The employer doesn't file anything with USCIS for CPT. That means smaller companies or those without immigration infrastructure can still hire you on CPT. You do need them to complete Form I-9 and confirm they're willing to document your role for academic credit purposes.
How do I find Compliance Specialist employers open to CPT students?
Migrate Mate lets you search for employers with work-authorization filing history in compliance-related roles, which signals familiarity with F-1 work authorization. Regulated industries like financial services, healthcare, and pharmaceuticals are reliable targets because they're required to maintain compliance functions and often hire students for structured rotations.
What happens if I use more than 12 months of full-time CPT as a Compliance Specialist?
Using 12 or more months of full-time CPT eliminates your OPT eligibility entirely, including the STEM OPT extension. Part-time CPT, defined as 20 hours or fewer per week, doesn't count toward that limit regardless of how long you use it. If H-1B visa sponsorship is your next step, OPT eligibility matters, so track your CPT usage carefully with your DSO.
Which compliance specializations are easiest to connect to a CPT curriculum?
Roles in financial compliance, healthcare regulatory affairs, and data privacy connect most directly to graduate and undergraduate programs in finance, public health, and information systems. Compliance work tied to specific regulations like HIPAA, SEC reporting, or AML is easier for a DSO to approve because the regulatory framework usually appears as named coursework in your program.