1.Responsible for Supporting TQM and GMP Systems` to be consistent with ISO 9001 system.
2.Devising and establishing a company’ quality procedures, standards and specifications.
3.Directing other staff on the review and auditing of documentation for compliance to good documentation practices and to the technical requirements of directive documents (SOPs, protocols, directive documents, etc.).
4.Set a periodic internal auditing scheduled.
5.Leads any procedures deviation discovering, and set up CAPA, and OOS investigations.
6.Reviewing QA standards, studying existing policies and procedures, and interacting with employees to evaluate effectiveness of QA program.
7.Setting standards for quality as well as health and safety.
8.Making sure that manufacturing or production processes meets the international and local quality standards.
9.Defining quality procedures in conjunction with operating staff.
10.Setting up and maintaining controls and documentation procedures.
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