1. To continuously inspire learning and help acquire competencies (knowledge, attitudes, skills) of personnel in QC / QA matters and all across the organization on quality aspects such as CGMP and various international regulatory requirements.
2. To be responsible for the performance of the quality function of the Formulations Manufacturing Operations
3. To document and implement company's overall validation policy, its intent and approach, including the validation of production processes, cleaning procedures, analytical methods, in-process control test procedures, connected computerized systems, and persons responsible for designing review, approval and documentation of each validation phase.