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Synpac Pharmaceuticals Ltd
Main ResponsibilitiesPrepares and maintains GMP documentation, including validation protocol and reports of the activities in charge, including Risk A... Role: Quality Assurance, Category: Engineering:Scientific, Size: 201-500
QUALITY ASSURANCE VALIDATION EMPLOYEE: Synpac Pharmaceuticals Ltd
Main ResponsibilitiesPrepares and maintains GMP documentation, including validation protocol and reports of the activities in charge, including Risk Assessments, process validation, cleaning validation and cross-contamination. Coordinates activities related to process validation, cleaning validation and cross-contamination, ensuring compliance with approved protocols and procedures.
