Responsible for all activities in Solids Manufacturing Area

-Routine microbiological analysis for non-sterile products-Microbiological analysis for WFI and purified water-Performing antibiotic assay-Environmental monitoring for sterile and non-sterile areas-Sterility testing for Ampoules & Vials-Cleaning validation-Trend analysis-Performing full chemical and physical analysis for cephalosporins vials-Managing stability schedules and performing stability testing for all products-Documentation and reporting of… Show more -Routine microbiological analysis for non-sterile products-Microbiological analysis for WFI and purified water-Performing antibiotic assay-Environmental monitoring for sterile and non-sterile areas-Sterility testing for Ampoules & Vials-Cleaning validation-Trend analysis-Performing full chemical and physical analysis for cephalosporins vials-Managing stability schedules and performing stability testing for all products-Documentation and reporting of analytical results, deviations, Out of Trend (OOT) or out of specification (OOS) results according to GMP committing to cycle time-Communication with other departments to achieve sales plan-Complying with HSE requirements-LEAN team representative for Microbiology and cephalosporins laboratories-HSE team representative for Microbiology and cephalosporins laboratories-Managing products release on SAP system-Raw materials standardization Show less

Preparation and revision of marketing and advertising materials used in marketing for products & launches of new products in the medical field

- Batch manufacturing records review for Non-Sterile Products- Checking and reviewing the data to ensure its adherence to specified protocol according to GMP-Checking the finished goods samples -Performing all IPC tests done in the production area-Conducting Quality tours in Non-sterile production & packaging areas -Assure operators commitment to GMP regulations-Participate in proper documentation during production process-Check the presence of approved SOPs and… Show more - Batch manufacturing records review for Non-Sterile Products- Checking and reviewing the data to ensure its adherence to specified protocol according to GMP-Checking the finished goods samples -Performing all IPC tests done in the production area-Conducting Quality tours in Non-sterile production & packaging areas -Assure operators commitment to GMP regulations-Participate in proper documentation during production process-Check the presence of approved SOPs and check their implementation in the production areas Show less

-Routine microbiological analysis for non-sterile products-Microbiological analysis for WFI and purified water-Performing antibiotic assay-Environmental monitoring for sterile and non-sterile areas-Sterility testing for Ampoules