Job Details
Experience Needed:
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Education Level:
Salary:
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Skills And Tools:
Job Description
- Preparation Hard files to be submitted to CAPA
- Follow up submitted Hard files in CAPA & submission of its comments (if any) till Receiving Registration licenses.
In case of Re-Registration products:
- Re-Registration process is the same as New products except No Inquiry Request
For Imported Products:
Responsible for:
- For New products: Registration process is the same as in New local products (Box system)
- For Re-Registered products: Re-Registration process is the same as New products except No Inquiry Request
For products with change control (Variations – Supplier addition – Pack/volume addition- Manufacturing change – license holder change – Registration License extension – Requests to Scientific & Technical committee)
Responsible for:
- Preparation change control request to be submitted at CAPA
- Follow up change control request submitted in CAPA & submission of its comments (if found) till Receiving its approval
Registration data updates
Responsible for:
- Update Inquiry Request data
- Update hard file data
- Update change control data
For Imported pesticides:
Responsible for:
- Submission of registration file to government
- Follow up its Registration process & submission of its comments (if found) till Receiving Registration approval
- Submission of analysis file to CALP & AHRI
- Follow up analysis file & submission of its comments (if found) till Receiving its approval
- Follow up with the government for receiving Registration Licenses
Job Requirements
- Bachelor of Veterinary or pharmaceutical science
- Good English & good Arabic reading and writing
- 0-1 years of experience in the regulatory affairs
