Regulatory Affairs Supervisor

Arena Life Science Tehran

Posted 3 years ago

Job Description

● Handling registration and importation procedures of medicinal products and supplements in Iranian food and drug administration. ● Handling warehouse GMP requirements upon IFDA regulations, ISO 9001 and 22000. ● Responsible for abroad contract manufacturing and importation of medicinal products and supplements.

Requirements

● At least 5 years of experience in the regulatory field for the local. ● Mastery of warehouse GMP regulations. ● English proficiency in all writing, reading, speaking, and listening skills. ● Mastery of Window’s Office software. ● Mastery of registration and Importation processes of medicinal products and supplements upon Iranian Food and drug administration’s regulations. ● Mastery of TTAC website features and procedures: * Customs release * Consumption permit * Esalat label.

Employment Type

  • Full Time

Seniority

Details

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