Building Quality Management system with new structure of quality professionals for new company according to defined regulations

Quality Assurance Manager

1.Provide active support and participation in managing the Pharmaceutical Quality System.2.High level of competence using Microsoft word, Excel to create automated reports.3.Manage the day to day activities of a team of QA professionals.4.Ensuring that all QA Tests are carried out on time and in full.5.Measure quality KPIs and promote continuous quality improvements.6.Provide support to quality event management e.g. complaints handling, deviations and CAPA management.7.Change controls including label and other artwork changes.8.Prepare and manage QA documentation and reports.9.Provide support in regulatory submissions and upkeep of dossiers.10.Participate in supplier audits as required.11.Awareness of regulatory requirement and customer service expectations. 12.Effectively liaise with Management and other Team members.13.Provide QA input and support for projects including validation.14.Actively participate in the training and development of subordinates.15.Participate in the self-inspection program.16.Participate in the GMP training program.17.Co-ordination of the Annual Product Quality Review program.

managing QA departments including foundation documentation , validation and IPC system for sterile parenteral solution

Physical&Chemical analysis for bulk, intermediate ,finished product and validation samples according to GMP instructions.creation and updating QC documentation.Reviewing batch documents with issuance COA for finished product.calibration for instrumental devices in chemistry lab.