Posted:3 hours ago|
Platform:
Work from Office
Full Time
Witnessing of manufacturing processes for sterile drug products including cleaning, sanitization, environmental monitoring and personnel monitoring to ensure compliance with CGMP regulations and regulatory standards
Oversight of cleanroom behavior, contamination control and aseptic techniques
To report any observations to site operations and quality and ensure compliance to the observations
Review of media fill protocol and reports and witnessing aseptic process simulations
Review of batch documentation to ensure product quality, regulatory compliance and meeting ALCOA++ requirements
Review of environmental monitoring reports
Review of unplanned deviations and CAPA
Light Pharma
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