
Pharma Quality
5 days ago
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Perform routine sampling, testing, and documentation as per standard operating procedures (SOPs).Assist in preparation and review of batch manufacturing records and related documents.
Conduct in-process checks to ensure compliance with Good Manufacturing Practices (GMP).
Support in handling deviations, change controls, and CAPA (Corrective and Preventive Actions).Maintain proper documentation and ensure records are updated in accordance with regulatory requirements.
Knowledge of GMP, GLP, and quality guidelines.
Understanding of basic analytical techniques (HPLC, UV, Dissolution, Wet chemistry).
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