Quality Assurance Supervisor

2 months ago


Egypt Orchidia Pharmaceutical Industries Full time
  • Follow up GMP nbsp; regulations and procedures for quality management system
  • Ensure timely completion of QA procedures, manufacturing, and packaging and in- process sampling.
  • Report non-conformance nbsp; that are identified during nbsp; routine operations and in process
  • Monitoring all phases of manufacturing , packaging of products in compliance with relevant standard operating procedures and manufacturing practices
  • Review procedures and processes for accuracy and completion.
  • Audit suppliers and vendors to assure their compliance nbsp; with GMP nbsp; and GSP regulation nbsp; and customer quality requirements
  • Follow up on preventive maintenance plan and completion of maintenance tasks
  • Approval of batch record amp; release of finished products for marketing
  • Record GMP deviation reports and follow CAPA system
  • Check and investigate customers complaints up to corrective and preventive actions
  • Design internal auditing plan, conduct the plan and nbsp; follow up CAPA system
  • Product description amp; specification
  • Applied standard lists issue. nbsp;
  • Communication with notified body in registration purposes and audit notification, CAR follow up
  • Supervise , support the quality nbsp; assurance personnel
  • Formulate technical training programs nbsp; and schedules based on nbsp; nbsp;knowledge of identified training needs , company production processes, business systems , or changes in products nbsp; , procedures or services Follow up GMP nbsp; regulations and procedures for quality management system
  • Ensure timely completion of QA procedures, manufacturing, and packaging and in- process sampling.
  • Report non-conformance nbsp; that are identified during nbsp; routine operations and in process
  • Monitoring all phases of manufacturing , packaging of products in compliance with relevant standard operating procedures and manufacturing practices
  • Review procedures and processes for accuracy and completion.
  • Audit suppliers and vendors to assure their compliance nbsp; with GMP nbsp; and GSP regulation nbsp; and customer quality requirements
  • Follow up on preventive maintenance plan and completion of maintenance tasks
  • Approval of batch record amp; release of finished products for marketing
  • Record GMP deviation reports and follow CAPA system
  • Check and investigate customers complaints up to corrective and preventive actions
  • Design internal auditing plan, conduct the plan and nbsp; follow up CAPA system
  • Product description amp; specification
  • Applied standard lists issue. nbsp;
  • Communication with notified body in registration purposes and audit notification, CAR follow up


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