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Job Summary:
Responsible for supervising and executing equipment operation, visual inspection, and packing activities in compliance with GMP and quality protocols. The role involves documentation, coordination with cross-functional teams, equipment qualification, and QMS adherence.
Key Responsibilities:
We are one of the world’s leading producers of key Active Pharmaceutical Ingredients (APIs) and generic formulations with a presence in 140+ countries and backed by 30 years of experience in the pharma sector. We endeavour to serve patients by moulding science and technology into therapies to improve health outcomes and people’s lives.
Job ID: 122723435