\t\t\u062a\u0639\u0644\u0646 \u0634\u0631\u0643\u0629 \u062c\u0648\u0641\u0627\u0644\u064a \u0644\u0644\u0645\u0646\u062a\u062c\u0627\u062a \u0627\u0644\u0637\u0628\u064a\u0639\u064a\u0629 \u0639\u0646 \u062d\u0627\u062c\u062a\u0647\u0627 \u0644\u0645\u0648\u0638\u0641\u064a\u0646 \u0641\u064a \u0645\u062e\u062a\u0644\u0641 \u0627\u0644\u0627\u0642\u0633\u0627\u0645 \u2013 \u0642\u062f\u0645 \u0627\u0644\u0622\u0646<\/p>\n \u062a\u0639\u0644\u0646 \u0634\u0631\u0643\u0629 \u062c\u0648\u0641\u0627\u0644\u064a \u0644\u0644\u0645\u0646\u062a\u062c\u0627\u062a \u0627\u0644\u0637\u0628\u064a\u0639\u064a\u0629 \u0639\u0646 \u062d\u0627\u062c\u062a\u0647\u0627 \u0644\u0645\u0648\u0638\u0641\u064a\u0646 \u0641\u064a \u0645\u062e\u062a\u0644\u0641 \u0627\u0644\u0627\u0642\u0633\u0627\u0645 \u2013 \u0642\u062f\u0645 \u0627\u0644\u0622\u0646<\/p>\n \u0634\u0631\u0643\u0629 \u062c\u0648\u0641\u0627\u0644\u064a \u0644\u0644\u0645\u0646\u062a\u062c\u0627\u062a \u0627\u0644\u0637\u0628\u064a\u0639\u064a\u0629 \u0628\u062d\u0627\u062c\u0629 \u0627\u0644\u0649 :<\/p>\n 1- R&D Pharmaceutical formulator<\/p>\n Key Responsibilities:<\/p>\n \u2022 Design and perform formulation experiments for development of stable formulations for liquid and solid dosage forms and are in compliance with general Good Manufacturing Practices (GMP) regulations.<\/p>\n \u2022 Evaluate existing literatures, patents and develop non-infringing formulations for new products.<\/p>\n \u2022 Conduct physical and chemical studies. Chemical Studies are to be organized with R&D analytical department to finalize formulation trials.<\/p>\n \u2022 Develop manufacturing processes for R&D formulations so that the technology transfer is successful for large-scale batches.<\/p>\n \u2022 Participating in the design of pre-formulation, optimization, and performing small-scale trials and scale-up batches.<\/p>\n \u2022 Write\/review product development reports, batch records, process validation protocols and reports, method validation protocols and reports, method transfer protocols and reports, SOPs etc.<\/p>\n \u2022 Document all the product development activities in assigned laboratory notebooks. Manage multiple development projects and develop formulations in a timely manner.<\/p>\n Education and Experience:<\/p>\n \u2022 B.S. and \/or M.S. degree in Pharmacy, Pharmaceutical Chemical Engineering.<\/p>\n \u2022 0-2 years of experience, all interested candidates will be taken into consideration.<\/p>\n \u2022 English language: very good writing and conversation skills.<\/p>\n \u2022 Computer: Excellent in MS office, Outlook, and Excel.<\/p>\n \u2022 Hands-on experience with product processing and characterization equipment is a plus.<\/p>\n \u2022 Male.<\/p>\n Skills Required:<\/p>\n \u2022 Experience with solid and lipid formulation development.<\/p>\n \u2022 Basic Knowledge of both pharmaceutical products and R&D technical operations functions is preferred.<\/p>\n \u2022 Planning and logistics skills capable of effective integration of Drug Product (DP) deliverables and able to support details execution at the manufacturing site level is preferred.<\/p>\n \u2022 Demonstrate leadership in planning obligations and activities.<\/p>\n \u2022 Ability to foster team productivity and cohesiveness and to work collaboratively to execute, deliver and get results is desired.<\/p>\n \u2022 Ability to influence peers, superiors, and partners.<\/p>\n \u2022 Motivated, self- starter able to work independently with demonstrated problem solving skills.<\/p>\n If interested, send your updated CV mentioning \u201cR&D Pharmaceutical formulator\u201d in the email subject.<\/p>\n 2- R&D Analytical Research Analyst<\/p>\n Key Responsibilities:<\/p>\n Conducting physical and chemical tests for samples that are related to the analytical research department.<\/p>\n \u2022 Follow the GMP, GLP guidance regulations and internal SOPs rules<\/p>\n \u2022 Perform all the chemical and physical analysis activities<\/p>\n \u2022 Analyze, develop and validate the analytical methods<\/p>\n \u2022 Practice analytical troubleshooting considering the section SOPs\u2019 and GLP rules.<\/p>\n \u2022 weekly and monthly stability analysis plans with documentation of all stability results and final<\/p>\n summaries<\/p>\n \u2022 Initiate of out of specification (OOS) and Out of Trend (OOT) investigations<\/p>\n \u2022 Record any troubles related to the analytical tasks, testers, instruments, chemicals and the out of<\/p>\n specification results.<\/p>\n Education and Experience:<\/p>\n \u2022 Bachelor\u2019s Degree in Chemistry<\/p>\n \u2022 From 1-3 years of experience in a related field<\/p>\n If interested, send your updated CV mentioning \u201cR&D Analytical Research Analyst\u201d in the email subject.<\/p>\n \u062a\u0639\u0644\u0646 \u0634\u0631\u0643\u0629 \u062c\u0648\u0641\u0627\u0644\u064a \u0644\u0644\u0645\u0646\u062a\u062c\u0627\u062a \u0627\u0644\u0637\u0628\u064a\u0639\u064a\u0629 \u0639\u0646 \u062d\u0627\u062c\u062a\u0647\u0627 \u0644\u0641\u0646\u064a \u062a\u0631\u0643\u064a\u0628\u0627\u062a \u062f\u0648\u0627\u0626\u064a\u0629 \u0641\u064a \u0642\u0633\u0645 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<\/figure>\n