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Regulatory Administration Specialist

Cobel Darou Tehran

Posted 6 months ago

Job Description

- Registration of pharmaceutical products and raw materials to obtain a new license and timely action to extend current licenses. - Negotiation and follow ups the company’s issues with IRFDA. - Checking information and handling of items for all pharmaceutical products for release and distribution. - Carrying out clearance of goods in TTAC system, , and informing the commercial unit. - Negotiation with the manufacturing business partners and MNCs (for licensed products) to resolve problems and deviations during production and implementation of required changes. - Compilation and translation of Brochures and Artwork for company products. - Evaluation of invoices and proforma invoices related to drugs and raw materials for their import.

Requirements

- Experience: 2 years of relevant experiences in Pharmaceutical Companies - Education: Pharm D - Good knowledge of English Language (Writing and Reading) - Good skills in computer (Microsoft Office, Word, Excel, ...)

Job Category:

Healthcare - Pharmaceutical

Employement type:

Full Time

Job Category:

Healthcare - Pharmaceutical

Employement type:

Full Time

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