Document Control
Sisel International, LLCSpringville, UT
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Overview
Schedule
Full-time
Career level
Entry-level
Remote
On-site
Benefits
Career Development
Job Description
POSITION PURPOSE AND SCOPE:The Document Control Specialist is responsible for supporting and maintaining the company’s compliance with applicable quality standards. This includes oversight of cGMP practices, quality systems, documentation, product labeling. This role is critical in ensuring products are safe, effective, and compliant with all regulatory requirements.ESSENTIAL RESPONSIBILITIES:
- Review and approve all SOP’s, policies and cGMP documents.
- Review all Master Manufacturing Records, Batch Records, Test Records, and Supplier Specifications to ensure they meet federal or state regulations.
- Review and approve packaging records and finished product release documentation.
- Maintain specifications control, filings, and change history.
- Distribute quality system documents for review and authorization as required.
- Control and distribute all documents and specifications to proper internal contacts, suppliers, and contract manufacturers.
- Maintain the systems requirements, formats, and procedures to produce, approve, release, control and archive controlled Documents.
- Conduct periodic audits of SOPs, record, and report results to ensure alignment with updated processes and regulatory changes.
- Oversee and maintain the retain sample program in accordance with FDA CGMP and company requirements.
- Train and assist personnel in the use of specifications and SOPs.
- Update training database with employee training based on training records submitted to document control. Files and maintains the training files. Sends out companywide training notifications.
- Participate in regulatory and third-party audits.
- Cross train in other Quality related functions.
- Any other duties and/or responsibilities as assigned.
- Must be able to work well with others especially when editing or revising their documents.
- Must be willing to perform repetitious tasks such as updating forms, filling logs, copying, and scanning documents.
- Proficiency in Microsoft Office applications is required. Oracle experience a plus, but not required.
- Must be flexible and adaptable to a fast pace, changing environment.
- Possess a positive attitude; be an excellent team player.
- Familiar with Federal and State regulation concerning dietary supplement requirements.
- Good Organization Skills and extremely detail oriented.
- Ability to work under pressure, plan personal workload effectively and delegate.
- The ability read, speak and understand English.
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FAQs About Document Control Jobs at Sisel International, LLC
What is the work location for this position at Sisel International, LLC?
This job at Sisel International, LLC is located in Springville, UT, according to the details provided by the employer. Some roles may also include multiple work locations depending on the requirement.
What pay range can candidates expect for this role at Sisel International, LLC?
Employer has not shared pay details for this role.
What employment applies to this position at Sisel International, LLC?
Sisel International, LLC lists this role as a Full-time position.
What experience level is required for this role at Sisel International, LLC?
Sisel International, LLC is looking for a candidate with "Entry-level" experience level.
What benefits are offered by Sisel International, LLC for this role?
Sisel International, LLC offers Career Development for this position. Actual benefits may vary depending on the employer's policies and employment terms.
What is the process to apply for this position at Sisel International, LLC?
You can apply for this role at Sisel International, LLC either through Sonara's automated application system, which helps you submit applications 10X faster with minimal effort, or by applying manually using the direct link on the job page.