● Support all regulatory activities.
● Register products in the Food and Drug Organization (Iran).
● Ensure that drug products are manufactured and tested in accordance with laws of the Food and Drug Organization and cGMP.
● Update the company regarding any changes in the regulation of the Food and Drug Organization (Iran).
● Prepare and supervise packaging material artwork.
● Review the Batch Manufacturing Record (BMR) and Batch Packaging Record (BPR).
● Release finished products.
● Handle complaints.
● Handle recall.
Requirements
● Pharmacist (PharmD) with valid Pharma License.
● Three years of work experience in the pharmaceutical industry.
● Fluent in Microsoft Office.
● Fluent in English.
● Mastery of TTAC.
● Familiar with Chargoon and TTAC applications.
● Expert in preparing SOP.