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Quality Assurance Document Supervisor

Lancaster, South Carolina

Job description:

  • Initiating investigations, assessing NCRs to determine if they have the necessary information to be closed out.
  • Oversee the Finished Product Update spreadsheets, including downloading the recently packaged batches from SAP and ensuring the laboratory sample receipt dates are accurate.
  • Track individual reviewer metrics to determine if additional training or guidance is needed.
  • Ensure cross training is performed and documented for individuals within the QA Document Specialist group.
  • Establish and oversee an organized system for both buildings to meet turn-around time goals.
  • Establish and oversee an organized system to track the change control process.
  • Hold monthly team meetings to ensure both buildings are communicating and working together as a team.
  • 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.


Bachelors or Associates degree with 5 years' experience in a cGMP environment

Must have at least 3-5 years of experience in an FDA regulated manufacturing environment, with 3 years specifically in Quality Assurance or Quality Control.

Why is This a Great Opportunity:

Stable company with growth potential!

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