Job Description

Job Summary:

Responsible for review and approval of Deviations and CAPAs in support of GMP manufacturing operations. Support timely review of events for classification, initiation in EtQ and closure. Support external client review and resolution of comments for assigned deviations and CAPAs as needed. Mentors junior QA staff in deviation/CAPA review and approval to include training and certification of QA approvers. Provide metrics to management as requested.

Job Responsibilities:

  • Works directly with Manufacturing, QA and other departments responsible for GMP activities to resolve production related deviations and other compliance issues in a timely manner. Review and approve Deviations and CAPAs
  • Facilitates triage meetings, performing classifications of DTRs
  • Collaborates with functional areas to improve the Deviation/CAPA system to include support in development of training materials and training personnel. Works to streamline these processes.

    • Ready to Apply?

    Take the next step in your AI career. Submit your application to KBI Biopharma today.

    Submit Application

    Job Details

    Location
    Durham, North Carolina, United States
    Job Type
    Full time
    Category
    Business Operations Specialists
    Posted Date
    July 04, 2026
    Deadline
    August 13, 2026