Quality Inspector - 3rd Shift

Moss Interactive, LLC; Rocky Mount (VA); On-site; USD 46,000 - 58,000; Full time

Benefits offered by this job

Shift differential 15%

Job summary

The Quality Inspector on 3rd Shift (11pm - 7:30am) at Traditional Medicinals, Inc. in Rocky Mount, VA, performs quality inspections of in-process and packaged goods and supports remediation tasks.

You will work under the Quality Manager to ensure compliance with procedures and standards across manufacturing and packaging operations. Responsibilities include documenting data, verifying logs, stopping production when quality issues arise, and assisting with corrective actions and administrative

Qualifications

• High school diploma or equivalent required.
• 1 year QA experience in food, wine, pharma, or supplements manufacturing preferred.
• Ability to read, interpret and apply quality standards, SOPs and work instructions.

Responsibilities

• Perform in-process quality checks on machine logs, data and components.
• Verify downstream packaging data and product procedures for quality.
• Alert production staff to stop production if quality problems are identified.
• Assist with investigation tasks and corrective action implementation.
• Assist with writing, compiling and reporting quality results and SOPs.

Skills

Analytical skills

Problem solving

Strong written communication

Strong verbal communication

Attention to detail

Team collaboration

Education

High school diploma or equivalent

Tools

MS Office

Production Management Software (RedZone)

Job description

Rocky Mount, Virginia, WV Full Time Manufacturing and Production Posted 08/11/2026

SUMMARY

The Quality Inspector on 3rd Shift (11pm - 7:30am) reports to the Quality Manager and performs quality inspections and ensures quality problem resolution for product manufacturing and packaging according to procedures, specifications and standards. This position also assists the Quality department with administrative aspects of quality maintenance and remediation.

ESSENTIAL FUNCTIONS

• In-process quality checks (IMA) – perform visual and physical verification of IMA machine production logs, data and components; assist with documentation and segregation of nonconforming components; collect/document samples and deliver to QC
• In-process quality checks (Downstream) – perform visual and physical verification of data, products and procedures throughout packaging, labeling, etc.
• Alert production staff to stop production if quality problems are identified
• Problem solves with production staff to achieve prompt resolution of identified quality issues
• Set up verifications (IMA) – Verify information, paperwork, logs, blends and components are correct against work orders and properly staged and that samples are available at each machine prior to production
• Changeover verifications (IMA) – Verify that previous product is fully cleared from IMA and downstream production and that new product information is correctly entered
• GMP facility walks - Identify and correct GMP violations or inconsistencies in quality procedures
• MBR end of run review – verify that documentation is complete for the production run after changeovers
• MBR review – perform final verification of MBR data to work order

ADDITIONAL DUTIES

• Assist with investigative tasks in the Quality Department
• Assist in deviation report generation or development and implementation of corrective action plans
• Assist with report writing, compiling and reporting results, SOP revisions and work instructions
• Provide administrative support to the department
• Other duties as assigned

REQUIREMENTS

• High school graduate or equivalent
• 1 year QA experience in food, wine, pharma, or supplements manufacturing facility preferred.

Knowledge/Abilities/Skills:

• Intermediate mathematics skills including percentages
• Conversant with units of measure such as grams or pounds
• Able to solve problems and make decisions based on company and/or quality policy
• Ability to read, interpret and apply quality standards, SOP’s, specifications and work instructions
• Strong analytical and problem-solving skills
• Strong organization and detailed skills
• Strong verbal and written communication skills
• Strong interpersonal skills
• Commitment to and ability to demonstrate TM’s Company values: humility, respect, quality, collaboration, innovation and sustainability

Technical Skills:

• Intermediate MS Office skills
• Production Management Software (RedZone preferred)

Work Environment:

Fast paced production environment working across all areas of production including IMA, blending, Mezzanine, case packers, display area, and QC lab

Compensation:

• $22.15 to $28.00 per hour
• 15% Shift Differential Provided
• No Relocation Assistance provided

Traditional Medicinals, Inc. and its subsidiaries are proud equal-opportunity employers.

We wholeheartedly embrace authenticity, diversity, and people's differences.

We acknowledge, celebrate, and support individuality to the great advantage of our consumers, stakeholders, products, and the planet.

We are committed to building an inclusive workplace for all our people.

We do not discriminate based on race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.