-
Job Description
Create a rolling QC plan based on lab workload and constraints, assess QC lab capacity, liaise with logistics, monitor plan execution, review site plans, and propose resolutions for lab bottlenecks. Monitor contract lab performance, escalate issues, and initiate change controls. Drive continuous improvement and metrics to measure QC performance.
Degree in Science, Engineering, or relevant discipline with GMP experience.
2-3 years experience in Quality Control, Quality Assurance, or Pharmaceutical/Biological Operations.
Quality Planning and Project Management skills with knowledge of GMP principles.
Key Responsibilities:
Create a rolling QC plan based on lab workload and constraints.
Assess QC lab capacity and liaise with logistics.
Monitor plan execution and review site plans.
Propose resolutions for lab bottlenecks and monitor contract lab performance.
Escalate issues and initiate change controls.
Drive continuous improvement and metrics to measure QC performance.
Requirements:
Degree in Science, Engineering, or relevant discipline with GMP experience.
2-3 years experience in Quality Control, Quality Assurance, or Pharmaceutical/Biological Operations.
Quality Planning and Project Management skills with knowledge of GMP principles.
Benefits:
Excellent opportunity with a leading multinational in the pharmaceutical industry.
Collaborative and dynamic work environment.
Opportunities for professional growth and development.