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About the 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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