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Regulatory Affairs Supervisor

Optimarc pharma
Sheraton, Cairo

Regulatory Affairs Supervisor

Sheraton, CairoPosted 9 days ago
10Applicants for1 open position
  • 5Viewed
  • 0In Consideration
  • 0Not Selected

Job Details

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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. 

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