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# Quality Assurance Technician

- **Company:** FACTORY6, INC.
- **Location:** Lindon, UT, United States
- **Experience:** Experienced
- **Salary:** $43,680.0 - $49,920.0
- **Contract:** Permanent contract
- **Skills:** Microsoft Word, Microsoft Excel, Microsoft Outlook, Microsoft Office, Gsuite
- **Published:** June 13, 2026
- **Apply:** https://www.indeed.com/viewjob?jk=77c0b80926c0232f

## About the Role

Do you have experience in Regulatory compliance?, Do you have a High school diploma or GED?, * 2-3 years of experience in Quality Assurance, Quality Control, or related role within dietary supplements, food, or pharmaceuticals

 * Knowledge of cGMP, FDA, and HACCP principles
 * Strong attention to detail and documentation accuracy
 * Excellent analytical and problem-solving abilities
 * Proficient in Microsoft Office (Excel, Word, Outlook) or Google workspace
 * High school diploma or GED

Preferred:

 * Experience with quality systems (e.g., HACCP, SQF)
 * Familiarity with dietary supplement manufacturing equipment and processes
 * Prior experience in a cGMP-regulated environment
 * Associate or Bachelor's degree in Biology, Chemistry, Food Science, or related field (or equivalent experience)

Skills & Competencies

 * Ability to conduct and interpret quality control analyses of raw materials and finished goods.
 * High attention to detail, reliability, and ethical integrity.
 * Excellent organizational and time management skills.
 * Effective communication and collaboration across various teams.

## Description

We are seeking a Quality Assurance Technician that plays a key role in ensuring all Factory6 dietary supplements meet the highest standards of safety, purity, and efficacy. This role supports production through in-process checks, material sampling, documentation, and adherence to cGMP and FDA regulations. The QA Technician collaborates closely with Production, and Regulatory teams to maintain compliance and continuous quality improvement., * Perform in-process quality checks during manufacturing stages (weighing, blending, encapsulation, packaging, etc.)

 * Sample and test incoming raw materials, in-process materials, and finished products
 * Conduct inspections and release finished goods according to established specifications
 * Investigate and document deviations, non-conformances, and participate in CAPA (Corrective and Preventive Action) processes
 * Assist in internal audits, customer audits, and regulatory inspections (FDA, third-party, etc.)
 * Maintain detailed and accurate quality records for traceability and compliance.
 * Support updates to quality procedures, SOPs, and work instructions.
 * Collaborate with other departments to identify and implement process improvements.


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