Quality Inspector - 3rd Shift

Traditional Medicinals•Rock Mount, VA

2d•$22 - $28•Onsite

About The Position

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.

Requirements

High school graduate or equivalent
1 year QA experience in food, wine, pharma, or supplements manufacturing facility preferred.
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
Intermediate MS Office skills
Production Management Software (RedZone preferred)

Responsibilities

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.
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 solve with production staff to achieve prompt resolution of identified quality issues.
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.
Verify that previous product is fully cleared from IMA and downstream production and that new product information is correctly entered.
Identify and correct GMP violations or inconsistencies in quality procedures.
Verify that documentation is complete for the production run after changeovers.
Perform final verification of MBR data to work order.
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.