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Quality Assurance Generalist (3rd Shift)

Location : Rock Hill, SC
Job Type : Direct
Reference Code : CRC_QAG3
Hours : Full Time
Required Years of Experience : 1+
Required Education : High School Diploma or GED
Travel : No
Relocation : No
Industry : Pharmaceutical

Job Description :


  • Reputable manufacturer of specialty health products who are industry leaders in setting and adhering to high standards in manufacturing and quality control.

  • Company focuses on researching and developing products to promote consumer health and is highly regarded in the industry for their advancements in the medical space.



·         The Quality Assurance Generalist I (QAG I) reports to the Quality Assurance Supervisor.

·         This position is responsible for the daily Quality Assurance support in the Manufacturing and Packaging process on site.

·         They will be required to review all appropriate documents during the production process.

·         In this role, the QAG I will be readily available to support the production process; therefore, this position requires that the associate stays on the production floor for the majority of the work day.

·         Providing Quality Assurance presence in the manufacturing and packaging areas through the execution of daily Packaging line and room clearances, In-process inspections, and issuing and tracking of Batch Records.

  • Providing input during the revision process of SOPs to cover the work required in the South Carolina facility.

  • Assisting in the investigation and closing of deviations.

  • Providing impact on issues that could affect product quality, safety and purity.

  • Reviewing the preventative maintenance, pest control and calibration records, etc.

  • Assisting with the trending and developing metrics to indicate quality system health of the organization.

  • Assisting Quality Assurance management with the daily operation of the QA Hold area.

  • Must be able to effectively communicate with other departments and function within a team environment.

  • Training on all SOPs, safety procedures and cGMPs as required

  • Evaluate and process returned products.

  • Other duties as assigned.

  • This position will be closely associated and work with the following:

    • Manufacturing and Packaging Operators

    • Quality Associates (QAG II, QA Supervisor, QC, Label Issuance, and Document Control Center)

    • Safety, Security and Environmental Services Manager

    • Training Coordinator

    • Supply Chain Team

    • Product Development

  • Perform other assigned duties as may be required in meeting company objectives

  • Regular attendance is required.

  • Communicate effectively with other departments within the organization and function within a team environment.

Required Qualifications :


  • 2+ years’ experience in the pharmaceutical or dietary supplement manufacturing environment preferred.

  • Auditing experience and troubleshooting is a plus.

  • High School Diploma or equivalent required.

  • Great enthusiasm and hard work ethic is a must.

  • The ability to lift 50lbs.

  • Detail oriented and team centered approach is required.

  • Good computer skills on all general software is needed MS Excel, MS Word, Lotus Notes, etc.



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