QA Supervisor - Regulatory Affairs Jobs In Egypt And Career In Rameda Pharmaceuticals Vacancies In Giza 2016
Employer Rameda Pharmaceuticals
Job Title QA Supervisor - Regulatory Affairs
Vacancy Deadline(mm/dd/yy) 4/29/2016
Languages English, Excellent
Country Egypt
City Giza
Job Category Pharmacy
Job Type Full Time
Job Level Senior
1- Member of internal audit and preparation internal audit check list. 2- Able to provide technical assessment for controlled document changes. 3- Responsible for implement the frequency of environmental tests and follow up investigation of unexpected result. 4- Able to prepare and review SOPs and controlled document. 5- Issuing, handling and reviewing of production batches. 6- Investigate product complained. 7- Gathering data and preparation of annual product review. 8- Able to review all registered document. 9- Performing follow-up for CAPA. 10- Responsible for MOH system , revising documents and license of Products, for new launches, free medical samples. 11- Contacts and host the MOH inspector. 12- collects all reports and documents needed for sampling and release 13- of products. 14- revise registration files and contact all departments to collect 15- documents required for product re-registration 16- Ensures that all activities in his unit or section are done according the relevant cGMP and ISO standards (ISO 9001/2008 , ISO 14001/2004 , OHSAS 18001/2007).
Qualifications BSc of Pharmacy or chemistry experience of at least 5 experiences, excellent in English, Computer skills, flexibility, effective communication skills, Ability to solve problems.
Gender Any
Car owner Any
Education major Pharmacy
Experience 4 - 5 Years.
Other Skills Good Communication skills, Analytical character, result oriented, self-motivated Education BSc of Pharmacy
Salary (L.E.) Negotiable
Comments Location in 6 of October
Job Contact Email Please send your CV to the following mail address quoting job title, career@rameda.com
QA Supervisor - Regulatory Affairs Jobs In Egypt And Career In Rameda Pharmaceuticals Vacancies In Giza 2016
Employer Rameda Pharmaceuticals
Job Title QA Supervisor - Regulatory Affairs
Vacancy Deadline(mm/dd/yy) 4/29/2016
Languages English, Excellent
Country Egypt
City Giza
Job Category Pharmacy
Job Type Full Time
Job Level Senior
1- Member of internal audit and preparation internal audit check list. 2- Able to provide technical assessment for controlled document changes. 3- Responsible for implement the frequency of environmental tests and follow up investigation of unexpected result. 4- Able to prepare and review SOPs and controlled document. 5- Issuing, handling and reviewing of production batches. 6- Investigate product complained. 7- Gathering data and preparation of annual product review. 8- Able to review all registered document. 9- Performing follow-up for CAPA. 10- Responsible for MOH system , revising documents and license of Products, for new launches, free medical samples. 11- Contacts and host the MOH inspector. 12- collects all reports and documents needed for sampling and release 13- of products. 14- revise registration files and contact all departments to collect 15- documents required for product re-registration 16- Ensures that all activities in his unit or section are done according the relevant cGMP and ISO standards (ISO 9001/2008 , ISO 14001/2004 , OHSAS 18001/2007).
Qualifications BSc of Pharmacy or chemistry experience of at least 5 experiences, excellent in English, Computer skills, flexibility, effective communication skills, Ability to solve problems.
Gender Any
Car owner Any
Education major Pharmacy
Experience 4 - 5 Years.
Other Skills Good Communication skills, Analytical character, result oriented, self-motivated Education BSc of Pharmacy
Salary (L.E.) Negotiable
Comments Location in 6 of October
Job Contact Email Please send your CV to the following mail address quoting job title, career@rameda.com
QA Supervisor - Regulatory Affairs Jobs In Egypt And Career In Rameda Pharmaceuticals Vacancies In Giza 2016