Regulatory Affairs Supervisor
دوام كامل
في Optimarc pharma
في
Egypt
نُشرت يوم December 17, 2024
تفاصيل الوظيفة
Job Description
Key Responsibilities: · Prepare and submit all documents required for import approvals, customs release, and exemptions. · Follow up and respond to Health Authorities’ inquiries until final approvals are granted. · Handle all Health Authorities visits (EDA & NFSA). · Stay updated with new Health Authority regulations. · Support the Marketing team with Health Authority-related inquiries. · Prepare registration dossiers for company products. · Maintain records for submitted documents and approvals. · Issue ACID requests and manage Nafeza platform-related issues. · Oversee EDA audit visits ensuring compliance and audit readiness. · Supervise the regulatory team and manage their work plan.Job Requirements
Qualifications: · Bachelor’s degree in Pharmacy. · Fluency in English and Arabic (spoken & written). · 3+ years of Regulatory Affairs experience (Raw Materials; Finished Products preferred). · High level of accuracy. · Strong communication and negotiation skills. · Effective problem-solving and time management abilities.Apply safely
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