1-responsible for registration of the company's products at the ministry of health. Configure the technical file Submit the file for the registration of pharmacological policies Follow the registration file and resolve any problems Receive the registration notice 2-Communicate with external suppliers to request certificates complete the required documents for registration. 3-Make electronic classification and book keeping for all certificate and notification of registration in such a way as facilitate reference when needed. 4-Continue to receive and update registration certificates before the expire. 5-Add codes and make adjustments to registration notification. 6-Responsible for presence with the pharmaceutical inspection and its presence with the values procurement and shipping. 7-Responosible for providing samples for the ministry of health laboratories and receiving the results of the analysis.
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