Quality Control Technician: cGMP-Driven QA in Nutraceuticals

factory6-job-board; Lindon (UT); On-site; USD 29,000 - 33,000; Full time

Benefits offered by this job

401K with employer match

Medical, dental, vision

Paid time off

Company holidays

Job summary

Factory6 is seeking a Quality Control (QC) Technician to ensure dietary supplements meet safety, purity, and efficacy standards. This role supports production with in-process checks, material sampling, documentation, and adherence to cGMP and FDA regulations.

Collaborate with Production and regulatory teams to maintain compliance and drive continuous quality improvements. 2–3 years in QA/QC is preferred; strong attention to detail and MS Office/Google Workspace skills are required.

Qualifications

• 2–3 years in Quality Assurance/Quality Control in dietary supplements, food, or pharma.
• Knowledge of cGMP, FDA, and HACCP principles.
• Strong attention to detail and documentation accuracy.
• Excellent analytical and problem-solving abilities.
• Proficient in Microsoft Office or Google Workspace.

Responsibilities

• Perform in-process quality checks during manufacturing stages (weighing, blending, encapsulation, packaging).
• Sample and test incoming raw materials, in-process materials, and finished products.
• Conduct inspections and release finished goods according to specs.
• Investigate deviations and participate in CAPA processes.
• Assist in internal and regulatory audits (FDA, third-party).
• Maintain detailed quality records for traceability and compliance.
• Support updates to quality procedures, SOPs, and work instructions.
• Collaborate with other departments to implement process improvements.

Skills

Quality control

Attention to detail

Analytical thinking

Documentation

Communication

Education

High school diploma or GED

Associate or Bachelor’s in Biology/ Chemistry/ Food Science

Tools

Microsoft Excel

Microsoft Word

Outlook

Google Workspace

Job description

Factory6 is seeking a Quality Control (QC) Technician to ensure dietary supplements meet safety, purity, and efficacy standards. This role supports production with in-process checks, material sampling, documentation, and adherence to cGMP and FDA regulations.

Collaborate with Production and regulatory teams to maintain compliance and drive continuous quality improvements. 2–3 years in QA/QC is preferred; strong attention to detail and MS Office/Google Workspace skills are required.