Περιγραφή εργασίας

The Regulatory Affairs Officer supports the company’s compliance with national and international pharmaceutical regulations governing the wholesale distribution of medicines and medical products. The role focuses on assisting with product registrations, regulatory documentation, licensing, and ensuring that all operations comply with Good Distribution Practice (GDP) and applicable regulatory authority requirements.
Knowledge/experience in quality and PV are a plus.

Brief Key Responsibilities – 

• Assist with preparation and submission of product registration and renewal applications
• Maintain regulatory files, licenses, and product documentation
• Track expiry dates of product registrations, permits, and company licenses
• Support compliance with pharmaceutical distribution regulations and GDP
• Liaise with suppliers and authorities to obtain required regulatory documents
• Support audits, inspections, and regulatory reporting
• Provide regulatory support to internal departments

TO APPLY: PLEASE EMAIL YOUR CV IN PDF ONLY TO: E.TAWIL@MAPHARMAGROUP.COM

Πώς να υποβάλετε αίτηση

Οι ενδιαφερόμενοι υποψήφιοι παρακαλούνται να στείλουν το βιογραφικό τους στον Διευθυντή Ανθρώπινου Δυναμικού στο e.tawil@mapharmagroup.com.

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Σχετικά με την εταιρεία

MA Pharmaceuticals