Regulatory Affairs Specialist

Registration - Egypt - Cairo
2021-02-16 02:16:00

About us :

Devartlab is a national company specialized in the field of pharmaceutical industries in the Egyptian market with a workforce covering all Egypt under the slogan of “Together for a worthy life” since 2011, Devartlab strives to be a leader in the field of nutraceutical and cosmeceutical products in the Middle East. The company has set a benchmark for discovering, developing, manufacturing and marketing such products over the past years in the Middle East and Africa.

Devart Lab started marketing its products in the Gulf markets since 2018 starting from Oman and the UAE and we have expanded the business in several new markets to cover sport nutrition, fast moving healthy foods & medicines that address many chronic diseases. In addition, we established two factories, one specialized in dietary supplements and special foods and the other is specialized in manufacturing and producing various pharmaceuticals.

Job Description:

  • Collect and coordinate information, prepare regulatory documentation for submission and follow up the registration process until getting the registration license
  • Solving problems related to registration of the products according to the requirements  
  • Establishes and maintains business relationships with official regulatory authorities.
  • Timely compile materials for license renewals, updates, and registrations
  • Maintain regulatory files/database and chronologies in good order.
  • Establish and maintain system for tracking changes in documents submitted to agencies or partners
  • Responsible for preparation of Registration files for any new product.
  • Responsible for creating Designs for New products.
  • Responsible for Registration of Cosmetics & Medical devices in EDA.
  • Responsible for Registration of Food Supplement and Special Nutrition in NFSA.
  • Responsible for following steps of formulations and stability study of any New products.
  • Responsible for getting Release permeation for any Shipment from EDA.
  • Responsible for following the Analysis Certificates from EDA.
  • Follow up with internal related company departments and external entities involved in the registration process
  • Preparing documents for authorization in embassies and offices of the ministry of foreign affairs required for products registration

Job Requirements

  • Bachelor of pharmaceutical sciences
  • 1-2 years’ experience in similar position “cosmetics, NFSA experience is preferred”
  • Excellent computer skills
  • Excellent written and verbal communication skills organization and planning
  • Problem analysis and problem-solving
Title ID:RS

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Job Title

Regulatory Affairs Specialist