Associate quality manager
Dabur Egypt Limited
Total des années d'expérience :17 years, 0 Mois
Job Title: Associate quality manager (starting as Chemist - Quality Officer - Quality Executive)
Tasks:
- In Process Control Section, That Include:
- Handling and follow up all Raw material lab activities.
- Handling and follow up all Processes inside factory as Product manufacture, packing activity, finished product inspection and release…
- Handling and follow up with all the quality Inspectors for monitor all the Processes.
- Control the Manufacturing System Practices of all Products which include the personal behavior of the employees.
- Monitor the critical control points & work environment and Supervision of the health situation and tools.
- Maintain the Work Instructions in accordance with Quality standards.
- Conduct effective Audit programs and Monitor the audits as per Schedule.
- Conduct compliance audits in accordance with the Quality standards in order to determine Compliance the Organizational Policies & procedures with the Quality Standards.
- Develop formal written reports (Identify process for the department being audited, controls and weakness, observation and recommendation with the staff being audited) to communicate audit results.
- Identifies the Non-Conformity cases within a process area in place to mitigate those non-conformities.
- Follow-up to determine adequacy of corrective actions & ensuring the closure of NCs in time.
- Keeps records of Non-Conformities from audits of problems, defects and operating statistics from Departments.
- Promotes Quality awareness to the staff and provides Quality awareness to newly hired personnel
- Conducting for Plans, Prepares and implementation of different training courses to ensure continues improvements for the Quality.
- Putting down GMP SOPs, instructions and records.
- Ensuring the compliance of GMP documents with local and International Standards.
- - Batch Record review.
- Investigate Quality Incidents/deviations.
- Perform GMP audits on site and vendors.
- Review validation, Qualification documents.
- Record and report deviations and incidents.
- Follow up complaints, Document Control Admin
- Deal with the MOH Inspectors for (all factory activates)
•Work as Manufacture and Production Chemist for the first 4 months.
•Work as Quality Assuarance and Quality Control Chemist till now.
•Responsiable for for Parachute products analysis including Raw material, packing material, semi- finish good by using different analytical techinque.
•Responsiable for Micro-analysis for Finish products and follow up of all the online processes inside the factory as production processes and manufacture processes.
•Responsiable for dealing With the ministry of Health in all the related processes as Pharmacy release for Raw material and the GMP Audit
•Internal Auditor.
•Responsiable for Dispatch process of the final products to different Countary
•Responsiable for all the Standeiztion and calibration processes inside the factory
Responsiable for The process of external Calibration for all the machine inside the factory
• Responsible for all the Q-Assurance systems.
•Standardization of Lab activities through benchmarking exercise with other products.
• Q-cert., drive inclusive of all new initiatives of CQA such as Mould management etc.
• Analysis reports and timely results.
• Adherence to PQA audit, report calendar and gap closures.
• Active participation in all Q-cert. improvement drives.
• Participation in Community Events.
Medical Rep. at Nelsen Pharmaceuticals Company
→Working in Para cytology, Bacteriology, Hematology, chemistry and virology unit.
Diploma of Biochemical analysis Faculty of Science Ain Shams University
- B. Sc. Degree : Of Chemistry and Zoology , Faculty Of Science, Helwan University General grade : Four years Percentage : (Good -73.9 % ) - May 2007 - Diploma of Biochemical analysis , Faculty of Science , Ain Shams University