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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
Skills:
Manual Visual Inspection MVI Techniques, Automated Visual Inspection AVI Operations, Logbook Documentation Management, Container Closure Integrity CCI Testing, Particulate Matter Detection, Re-Inspection Reconciliation Procedures, Defect Categorization Classification
Skills:
process monitoring, Deviation Handling, Team Supervision, Pharmaceutical Production, BMR Documentation, GMP SOP Compliance
Skills:
Aseptic operations, Lyophilizer handling, Steam sterilizer operation, Equipment cleaning, Media fill support, Filter integrity testing
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