إنتهت صلاحية هذا الإعلان الوظيفي لقد إنتهت صلاحية هذا الإعلان الوظيفي و هو غير مفتوح حاليا لأي طلبات عمل.
إرفاق
وصف الوظيفة
Participate in Translating business goals into plans that cover local market and export.
Participate in Preparation of new products stability files to be registered and launched onto the market in accordance with local regulatory requirements and requirements of export under the general supervision of the R&D manager.
Execute plan of stability studies covering first three batches, process validation, and change or add supplier, change composition & ongoing stability study covering for all products.
Monitor of stability temp. & humidity and ensure of archiving them
Prepare protocol for each stability studies containing summarized data and results.
send stability samples for micro analysis (sterility or preservative effectiveness test) for long, Acc. & in use
analysis of the new product under stability condition must meet the product specification especially impurities
update SOPs related to stability system & covering R&D activities
Report problems relating to products in stability chambers to R&D manager immediately.
Maintain & enhance capacity of stability chambers to cover different dosage form
Work according to R&D safety system.
Work according of GLP requirements
المهارات
Bachelor's degree a must, in Pharmaceutical science.
From 1 to 3 years of technical experience in stability, analytical method validation and training preferably in the pharmaceutical industry.
Scientific, technical background in pharmaceutical as well as cosmetics products is beneficial.
Using an advanced knowledge of stability and method validation techniques.
Excellent English, verbal / written communication.
Ability to communicate well and work through others.
Excellent computer skills.
Self-Motivating.
Creative.
Good problem solving skills.
Good communications skills.
Good self-management skills.
Capable of working in a team environment.
المؤهلات العلمية
Pharmacy