Regulatory Affairs Specialist at DEVARTLAB Pharmaceuticals

 

 

 

 

 

Devartlab is Looking for #regulatoryaffairs specialist to join the team

*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

To join us kindly send your updated CV mentioning ( RA specialist ) to
Heba.Osama@devartlab.com