Job Description
Job Summary:
Create a rolling QC plan based on laboratory workload and known constraints. Assess QC Laboratory capacity and liaise with logistics and warehouse personnel for sample schedules. Monitor plan execution, report KPIs, and propose mitigation plans.
Key Responsibilities:
Create a rolling QC plan based on laboratory workload and known constraints.
Assess QC Laboratory capacity and propose resolutions for laboratory bottlenecks.
Liaise with logistics and warehouse personnel for sample schedules.
Monitor plan execution, report KPIs, and propose mitigation plans.
Review mid to long-term site plans and perform scenario planning.
Manage change controls and deviations for the QC department.
Facilitate investigations, ensuring effective Root Cause Analysis and CAPAs.
Drive metrics to measure QC performance and take action to mitigate.
Requirements:
Degree in Science, Engineering, or relevant discipline.
Operational excellence in GMP environment.
Experience in planning and project management.
2-3 years experience in Quality Control, Quality Assurance, or Pharmaceutical or Biological Operations.
Skills:
Quality Planning
Project Management
GMP