Regulatory Affairs Specialist At Majestic Bio Pharma
Majestic Bio Pharma is hiring Regulatory Affairs Specialist
Requirements :
- Submission and following-up of registration & re-registration files for the company’s products (local and imported).
- Following-up on files submission to various committees until receiving the final registration licenses.
- Submission of files & samples to NODCAR and following-up the analysis of the company’s products until receiving the final conformity of the product.
- 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.)
- 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.
- Working closely with the department manager in revising final outer and inner packs data & issuing them from E.D.A. and revising final films from printing houses.
- Applying the company policies and work for achieving its goals according to the ethics, rules & regulations.
- Performing any other task assigned by the direct manager related to the field of work.
Job Requirements
- Bachelor’s degree from reputable university (Degree in Pharmacy, Veterinary Medicine, Science)
- Good Computer Skills (MS Office – Internet browsing
- Good English and Arabic (Written & Spoken)
- 1 - 3 Years of experience as Regulatory Affairs Specialist in Pharmaceutical Companies or Authority
- Good business relationships in different departments of EDA.
- Attending Communication Skills, Time Management and Negotiation Skills Courses is a plus.
Kindly if u are interested send you resume