Job Summary

• The role involves ensuring the smooth startup of the pMDI factory from a technical and process perspective while leading design and validation activities.
• Candidates will be responsible for establishing technical documentation, SOPs, and digital solutions to meet GMP/SHE requirements and improve process robustness.
• The position requires managing technical transfers, investigating process deviations, and driving cost reduction and yield improvement projects.

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Skills & Requirements

Key Requirements

• Experience in pharmaceutical process engineering
• Knowledge of GMP and SHE regulations
• Proficiency with SAP/MES systems
• Background in validation and qualification
• Strong analytical and problem-solving skills

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