Job Description
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 Show more Skills
Analysis Skillsunmatched
Biologyunmatched
Biotech and Pharmaceuticalunmatched
Check Processingunmatched
Chemistryunmatched
Communication Skillsunmatched
Corrective Actionunmatched
Corrective and Preventative Action (CAPA) Systemsunmatched
Current Good Manufacturing Practice (cGMP)unmatched
Detail Orientedunmatched
Documentationunmatched
FDA (Food and Drug Administration)unmatched
FDA Requirementsunmatched
Food Scienceunmatched
Health Planunmatched
High School Diplomaunmatched
Internal Auditunmatched
Maintain Complianceunmatched
Manufacturingunmatched
Manufacturing Equipmentunmatched
Manufacturing/Industrial Processesunmatched
Materials Analysisunmatched
Microsoft Excelunmatched
Microsoft Officeunmatched
Microsoft Outlookunmatched
Microsoft Wordunmatched
Organizational Skillsunmatched
Problem Solving Skillsunmatched
Process Improvementunmatched
Process Qualityunmatched
Production Supportunmatched
Quality Assuranceunmatched
Quality Controlunmatched
Quality Managementunmatched
Regulationsunmatched
Safety Standardsunmatched
Standard Operating Procedures (SOP)unmatched
Time Managementunmatched
Traceabilityunmatched
United States Department of Energy (DOE)unmatched
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