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Sr Administrative Services Coordinator

Greenville, North Carolina, USA💼 Full-time🗓 2026-09-14 → 2026-09-25

Core

Hands-on GMP documentation and production-support role ensuring accurate batch records and cGMP compliance in sterile manufacturing.

Role type

Administrative Services Coordinator (GMP Documentation)

Builds

Accurate production batch records and compliant documentation for sterile manufacturing operations

Domain

Pharmaceutical manufacturing / GMP compliance

Deliverable

production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work

Required skills

GMP/cGMP documentation practices, batch record review and reconciliation, discrepancy resolution, manufacturing system navigation, physical mobility in production areas

Preferred skills

Pharmaceutical batch record experience, cross-functional team partnering, SAP proficiency

Technologies

SAP

Responsibilities

Review completed production batch records for accuracy and cGMP compliance; Reconcile batch documentation and resolve discrepancies with Production and QA; Analyze recurring batch record errors to improve process efficiency; Support production operations while maintaining discretion and time management; Move between buildings and production areas as needed; Follow all site safety, GMP, and PPE requirements

Seniority

Individual Contributor, operational support

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