Regulatory Affairs Director – Hikma Pharmaceuticals
• Propose new plans and initiatives that would boost the effectiveness of the MENA Regulatory Affairs function.
• Ensure that work activities are carried out achieving the pre-set performance goals, and suggest any necessary actions to managers.
• Monitor and rationalize the related registration expenses.
• Maintain approved products registration, through responding to changes in regulations in MENA.
• Manage the registration of new products and respond to changes in regulations in MENA as well as execute regulatory registration activities including filings, labeling, and review.
• Evaluate new product dossiers for regulatory compliance and suitability while studying various options and optimize drug registration process.
• Manage the submission of pre-approval and post-approval registration dossiers for newly developed pharmaceutical products
• Foster strong relationships with decision makers in drug administrations, governmental parties, Ministries of Health in MENA, and similar committees and organizations to expedite approvals and smoothen the registration processes.
التقدم للوظيفة الان
أنشئ سيرتك الذاتية الآن و تواصل على الفور مع أكبر و أفضل الشركات اون لاين. إنشائك لسيرة ذاتية على موقع المازن.كوم هي الوسيلة الأكثر فعالية للحصول على الوظيفة Regulatory Affairs Director – Hikma Pharmaceuticals بكل سهولة الان مجانا.