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Regulatory Affairs Specialist

Atco Pharma For Pharmaceutical Industries
Cairo, Egypt
Posted 1 year ago
150Applicants for1 open position
  • 68Viewed
  • 0In Consideration
  • 0Not Selected
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Job Details

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Job Description

• Responsible for registration and re-registration of veterinary products.
• Responsible for preparation and submission of variation requests and follow up them till obtain approvals.
• Responsible for preparation and submission of Hard files and follow up them till obtain Registration Licenses.
• Responsible for preparation and submission of raw material transfer requests and follow up them till obtain approvals.
• Responsible for preparation and submission of stability studies and follow up them till obtain approvals.
• Responsible for preparation and submission of soft files and follow up them till obtain registration approvals.
• Responsible for preparation and submission of feed additives & Reg. and Re-Reg. files to ministry of agriculture and follow them till obtain registration certificate.
• Responsible for preparation and submission of the annual Importation plan of the APIS & its modifications.

Job Requirements

- Bachelor’s degree in pharmaceutical or veterinary medicine.
- Minimum 3 years of hands-on experience as a Regulatory Affair Specialist - Vet.
- Experience in dealing with governments & Competent government bodies. 
- High Communication Skills.
- High Command of English and Arabic languages.
- Resident: Cairo.

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