As part of the MPU Validation Platform supporting vaccine manufacturing operations, the consultant will be responsible for developing, maintaining, and optimizing a comprehensive database covering all Single Use Systems (SUS) utilized across manufacturing processes. This role will support traceability, compliance, standardization, and continuous improvement initiatives within a highly regulated pharmaceutical environment.

Key Responsibilities

• Identify and map Single Use Systems (SUS) and components used across manufacturing units.
• Collect, verify, and consolidate technical documentation related to SUS assemblies and materials.
• Build and maintain a structured and reliable database containing:
  • Component specifications
  • Supplier information
  • Bills of Materials (BOM)
  • Certificates of Compliance (CoC)
  • Material and validation data
• Ensure data integrity, accuracy, and consistency across all records.
• Collaborate with Validation, Quality Assurance, Manufacturing, Engineering, and Process teams to gather and validate information.
• Support change control, risk assessment, and regulatory compliance activities through accurate data management.
• Contribute to standardization initiatives across manufacturing sites and processes.
• Generate reports and dashboards to support operational and quality decision-making.
• Participate in continuous improvement projects related to SUS lifecycle management.