
Omar Ahmed Ismail
Quality Assurance Officer at Hikma Pharmaceuticals
Shebin Alkom, Monufya, EgyptWork Experience
Quality Assurance OfficerFull Time
Hikma Pharmaceuticals
Jul 2020 - Present -4 yrs, 11 months
Egypt , Giza
- Job Details:1- Follows all relevant quality instructions so that works is carried out in a controlled and consistent manner. 2- Follows the day-to-day operations related to own jobs in the function to ensure continuity of work. 3- Participates as a team member, under close supervision, and receives and carries out detailed instructions in order to grow professional capability. 4- Applies standard quality technique to provide solutions to problems involving a limited number of variables. 5- Applies technical knowledge, following established procedures and/or standard practices, to perform basic analyses 6- Participates in specific small projects related to own area of responsibility, allocated by superiors, within set terms of reference and defined processes. 7- Analyzes, resolves, and documents quality related queries and problems via interpretation of procedures and escalates them where necessary in order to meet quality standards. 8- Performs in-process check or documentation, following established procedures and/or standard practices, to perform basic analyses. 9- Complies with all relevant safety, quality, health and environment procedures to ensure a healthy and safe work environment.
Quality Assurance OfficerFull Time
Nerhadou
Jul 2019 - Jun 2020 -11 months
Egypt , Giza
- Job Details:1- Follow up procedures and ISO 9001 Quality Management System. 2- Execute all (IPC) activates done in the production areas. 3- Review of the finished batch records. 4- Control and Revision Standard Operating Procedures (SOPs), Formats, Documentation. 5- Retrieval, Control, Retention and destruction of all completed documents (records). 6- Revision & Control of Master Formula Card & Master Packaging Card. 7- Preparation, issuance &Retrieval and control of Master Production Record (Manufacturing & Packaging). 8- Review of Master Production Record (Manufacturing & Packaging). 9- Conducting regular investigations to guarantee that workers’ follow safety procedures as required. 10- Dispensing Review, Check export stages. 11- Ensuring compliance of plant conditions (Humidity, Temperature,…etc) with set guidelines. 12- Inspect Production Lines/areas for GMP compliance. 13- Sampling and testing of product during manufacturing, filling or packaging according to approved sample plans. 14- Sampling of blend and/or finished goods for QC release testing according to approved SOPs. 15- Complete and maintain quality and production records according to GMP. 16- Monitor the inspection line. 17- Prepared disinfected solutions (Alcohol 70%). 18- Review and develop Company SOPs when needed. 19- Documenting any and all problems/errors found. and reporting these to the appropriate department for correction. 20- Documents inspection results by completing reports and logs; summarizing re-work and waste; inputting data into quality database.
QA specialistFull Time
ATCO Pharma
Sep 2018 - Jun 2019 -9 months
Egypt , Monufya
- Job Details:1- Follow up procedures and ISO 9001 Quality Management System. 2- Execute all (IPC) activates done in the production areas. 3- Review of the finished batch records. 4- Control and Revision Standard Operating Procedures (SOPs), Formats, Documentation. 5- Retrieval, Control, Retention and destruction of all completed documents (records). 6- Revision & Control of Master Formula Card & Master Packaging Card. 7- Preparation, issuance &Retrieval and control of Master Production Record (Manufacturing & Packaging). 8- Review of Master Production Record (Manufacturing & Packaging). 9- Conducting regular investigations to guarantee that workers’ follow safety procedures as required. 10- Dispensing Review, Check export stages. 11- Ensuring compliance of plant conditions (Humidity, Temperature,…etc) with set guidelines. 12- Inspect Production Lines/areas for GMP compliance. 13- Sampling and testing of product during manufacturing, filling or packaging according to approved sample plans. 14- Sampling of blend and/or finished goods for QC release testing according to approved SOPs. 15- Complete and maintain quality and production records according to GMP. 16- Monitor the inspection line. 17- Prepared disinfected solutions (Alcohol 70%). 18- Review and develop Company SOPs when needed. 19- Documenting any and all problems/errors found. and reporting these to the appropriate department for correction. 20- Documents inspection results by completing reports and logs; summarizing re-work and waste; inputting data into quality database.
Education
Technical Diploma in Analytical Biochemistry
Menoufia UniversityJan 2019 - Jan 2020 - 1 Year
Bachelor's Degree in Chemistry
Menoufia UniversityJan 2014 - Jan 2017 - 3 yr
Languages
English
Fluent