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SIMTEC Silicone Parts

Quality Assurance & Compliance Intern

Entry-Level JobVerifiedNo experience needed

Career Insights for Document Control / Management Specialist

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What they do

A Document Control or Management Specialist manages written and electronic documents for an office or company. Develops or maintains systems for keeping track of documents, including labeling, retrieving, distributing, recovering and destroying documents as needed.

$41,892 / year median in Florida

+12% projected growth

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Job Description

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.
Full-Time/Part-Time Full-Time Exempt/Non-Exempt Non-Exempt Shift Days Location Simtec Description 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 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.