Microbiology Quality Control Analyst Jobs In Egypt And Career In Rameda Pharmaceuticals Vacancies In Cairo 2014
Employer Rameda Pharmaceuticals
Job Title Microbiology Quality Control Analyst
Languages English - Arabic
Country Egypt
Job Category Pharmacy, Quality Assurance, Quality Control
Job Type Full Time
Description 1- To analyze Raw Materials or Bulk or Intermediate or Finished Product (Microbiological testing) according to company procedures and using some reference books (USP, EP, BP, etc...) 2- To perform the Sterility testing for all sterile products. 3- To analyze the Qualification and Registration samples of new products and pre-market stability 4- To analyze the Cleaning Validation samples. 5- Perform Bulk and Finished Products Validation testing. 6- To analyze samples for the purified water and water for Injection of water systems. 7- To prepare and record the environmental viable monitoring results of production sterile areas (validation & routine). 8- To perform the Validation testing of equipment of Sterile areas 9- To perform the Routine & Validation environmental monitoring of sterility testing area of QC Lab (viable and particulate). 10- Evaluation of results and reports affect releasing the Raw Material to production. 11- Evaluation of results and reports affect releasing the finished product to the market. .
Qualifications 1- Science/Pharmacy Graduates 2- 1-2 Years of experience in reputable pharmaceutical company is preferable. 3- Excellent English and computer skills.
Gender Male
Experience 1 - 2 Years.
Other Skills - Good communication skills - Analytic Character. -Result oriented and self motivated.
Salary (L.E.) Negotiable
Comments plant is located in 6 October City
Job Contact Email please send your CV to the following mail address quoting Job Title. career@rameda.com -
Employer Rameda Pharmaceuticals
Job Title Microbiology Quality Control Analyst
Languages English - Arabic
Country Egypt
Job Category Pharmacy, Quality Assurance, Quality Control
Job Type Full Time
Description 1- To analyze Raw Materials or Bulk or Intermediate or Finished Product (Microbiological testing) according to company procedures and using some reference books (USP, EP, BP, etc...) 2- To perform the Sterility testing for all sterile products. 3- To analyze the Qualification and Registration samples of new products and pre-market stability 4- To analyze the Cleaning Validation samples. 5- Perform Bulk and Finished Products Validation testing. 6- To analyze samples for the purified water and water for Injection of water systems. 7- To prepare and record the environmental viable monitoring results of production sterile areas (validation & routine). 8- To perform the Validation testing of equipment of Sterile areas 9- To perform the Routine & Validation environmental monitoring of sterility testing area of QC Lab (viable and particulate). 10- Evaluation of results and reports affect releasing the Raw Material to production. 11- Evaluation of results and reports affect releasing the finished product to the market. .
Qualifications 1- Science/Pharmacy Graduates 2- 1-2 Years of experience in reputable pharmaceutical company is preferable. 3- Excellent English and computer skills.
Gender Male
Experience 1 - 2 Years.
Other Skills - Good communication skills - Analytic Character. -Result oriented and self motivated.
Salary (L.E.) Negotiable
Comments plant is located in 6 October City
Job Contact Email please send your CV to the following mail address quoting Job Title. career@rameda.com -
