About this role
Main Responsibilities: • Support and manage production equipment (e.g., pH meters, weighing scales) • Handle single-use systems (SUS) in manufacturing • Coordinate incoming material readiness • Drive process qualification (PQ) execution • Support DeltaV system operations (basic troubleshooting, run logic understanding) • Work with SAP for production coordination Requirements: • 5+ years in biopharma manufacturing • Strong GMP operations & qualification exposure • Hands-on shopfloor and equipment experience • Familiarity with DeltaV / automation environments Contract Duration: 12 months with options to renew based on performance
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