Demo

Quality Control Technician

Factory6
Lindon, UT Full Time
POSTED ON 9/19/2026
AVAILABLE BEFORE 10/18/2026
About Us

Factory6 is a contract manufacturer and co-packer with over 20 years of industry experience. We specialize in capsules, tablets, and beverage powders, delivering nutraceutical products that consumers love.

As a full-service development partner, we simplify the process while maintaining transparency and adhering to the highest quality standards. With a focus on innovation, operational excellence, and collaboration, we support brands in creating customized supplements packed with benefits and flavor, with customer satisfaction in mind.

About The Role

We are seeking a Quality Control (QC) Technician who 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 QC Technician collaborates closely with Production and regulatory teams to maintain compliance and continuous quality improvement.

Key Responsibilities

  • 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.

Qualifications

Required:

  • 2–3 years of experience in Quality Assurance, Quality Control, or a 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 Preferred
  • 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.
  • Close attention to detail, reliability, and ethical integrity.
  • Excellent organizational and time management skills.
  • Effective communication and collaboration across various teams.

Work Schedule

  • Day Shift 6:00 am - 4:30 pm
  • Swing Shift 2:00 pm 11:30 am
  • Workweek is Monday through Thursday
    • Opportunities for overtime are available on Fridays and Saturdays
Compensation

  • Hourly rate: Starting rate of $21.00 - $24.00 (DOE)
  • 401K with employer match
  • Full medical coverage with dental and vision options
  • Paid time off and company holidays

Salary : $21 - $24

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