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Regulatory Affairs Specialist

Macro Group
Sheraton, Cairo
Macro Group logo

Regulatory Affairs Specialist

Sheraton, CairoPosted 3 days ago
23Applicants for1 open position
  • 9Viewed
  • 3In Consideration
  • 0Not Selected

Job Details

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Job Description

1 Submission and following-up of registration & re-registration files for the company’s products (local and imported).
2 Following-up on files submission to various committees until receiving the final registration licenses.
3 Submission of files & samples to NODCAR and following-up the analysis of the company’s products until receiving the final conformity of the product.
4 Working closely with the department manager in issuing of all the requested certificates for the Export department. (For example: Free sale, GMP, copy of plant license …. etc.)
5 Working closely with the department manager in the process of releasing finished products, imported raw materials, imported research and development samples and imported packaging materials.
6 Working closely with the department manager in revising final outer and inner packs data & issuing them from M.O.H. and revising final films from printing houses.
7 Applying the company policies and work for achieving its goals according to the ethics, rules & regulations.
8 Performing any other task assigned by the direct manager related to the field of work.
 

Job Requirements

-Bsc. Of  Pharmacy
- Good Computer Skills (MS Office – Internet browsing)
- Good English and Arabic (Written & Spoken)
- 1 - 3 Years of experience as Regulatory Affairs Specialist in Medicated Cosmetic Companies

- Good business relationships in different departments of Ministry of Health.

- Attending Communication Skills, Time Management and Negotiation Skills Courses is a plus.
 

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