QA Inspector- Nutritional Supplements

Trove Brands • Lehi, UT

7d

About The Position

The Quality Inspector is responsible for ensuring that all raw materials, components, in-process blends, finished goods, and packaging used in our nutritional supplement manufacturing environment meet established quality standards. This role plays a critical part in safeguarding product integrity, supporting continuous improvement initiatives, and upholding compliance with cGMPs, internal specifications, and industry regulations. Perform visual, dimensional, and functional inspections of incoming raw materials, packaging components, and finished supplements. Conduct in-process check including blends, capsules, tablets, powders, and packaging line audits. Verify adherence to SOPs, quality standards, and cGMP requirements. Sample and test materials per established procedures and specifications. Identify defect, deviations, or inconsistencies and support root-cause investigations. Complete inspection records with precision and clarity while maintaining full traceability. Support documentation review for batch records, material COAs, and deviation reports. Ensure compliance with FDA, cGMP, and internal quality system requirements. Maintain accurate logs, inspection data, and digital quality records. Participate in continuous improvement activities, including process audits, corrective actions, and improvement initiatives. Identify trends, recurring issues, or opportunities for process enhancements. Support Training efforts by demonstrating proper inspection methods and quality standards. Contribute to building a culture of quality ownership and operational excellence.

Requirements

• 1-3 years of quality experience in nutritional supplements, food, beverage, pharmaceuticals, or related manufacturing.
• Strong understanding of cGMPs, FDA regulations, and quality documentation practices.
• High attention to detail with the ability to spot inconsistencies quickly.
• Comfortable working with measurement tools, inspection equipment, and sampling methods.
• Excellent communication skills and the ability to work effectively across teams.
• Proficiency with compute systems and quality documentation tools (ERP, QMS preferred).
• Ability to work in a dynamic environment with shifting priorities.

Responsibilities

• Perform visual, dimensional, and functional inspections of incoming raw materials, packaging components, and finished supplements.
• Conduct in-process check including blends, capsules, tablets, powders, and packaging line audits.
• Verify adherence to SOPs, quality standards, and cGMP requirements.
• Sample and test materials per established procedures and specifications.
• Identify defect, deviations, or inconsistencies and support root-cause investigations.
• Complete inspection records with precision and clarity while maintaining full traceability.
• Support documentation review for batch records, material COAs, and deviation reports.
• Ensure compliance with FDA, cGMP, and internal quality system requirements.
• Maintain accurate logs, inspection data, and digital quality records.
• Participate in continuous improvement activities, including process audits, corrective actions, and improvement initiatives.
• Identify trends, recurring issues, or opportunities for process enhancements.
• Support Training efforts by demonstrating proper inspection methods and quality standards.
• Contribute to building a culture of quality ownership and operational excellence.

Benefits

• Comprehensive medical, dental, and vision care
• 401k package with employer matching
• Paid Time Off
• Maternity/Paternity leave
• Full indoor basketball/volleyball court
• Fully equipped fitness center (cardio, weights, functional fitness area, lockers and showers, etc.)
• Yoga studio
• Meditation/Nap room

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: No Education Listed