Job Description

Ensure pharmaceutical manufacturing activities comply with GMP, regulatory and quality standards while supporting efficient production, maintaining accurate documentation, and assisting with shift operations.

Main Responsibilities

  • Support production activities to meet schedules
  • Verify products, equipment, materials, and production areas for GMP compliance
  • Review and approve production documentation, line clearances, and batch records
  • Ensure manufacturing processes comply with quality, GMP, and regulatory standards.
  • Investigate production issues and implement corrective actions
  • Initiate, investigate, document and close deviations.
  • Coordinate and assess change controls and its actions to ensure compliance and minimize compliance risk.
  • Develop and track Corrective and Preventive Actions (CAPAs) to address root causes and prevent recurrence
  • Drive process improvement initiatives to ...

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