Job Details
Experience Needed:
Career Level:
Education Level:
Salary:
Job Categories:
Skills And Tools:
Job Description
- Submission and following-up of registration & re-registration files for the company’s products (local and imported).
- Follow-up files presentation to various committees until receiving the final registration licenses.
- Submission files & samples and follow-up the analysis of new products in NODCAR until receiving the final conformity of the product.
- Follows up on issuing of Free Sale Certificates – GMP Certificates, a copy of the factory license issued by the CAPA.
- 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.
- Deputized from Regulatory Affairs Manager to revise final outer and inner packs data & issuing them from M.O.H. + revising final films from printing houses.
- Deputizing the regulatory affairs manager to attend meetings of M.O.H. and to deal with middle management in M.O.H.
- Deputizing the regulatory affairs manager to deal with different departments in the company in the absence of the direct manager.
- Responsible for the on job training of new employees in the department.
- 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
- B.Sc pharmacy ,Vet, Science
- Computer skills
- Legal knowledge
- Administrative skills
- Communication skills, problem-solving skills and strategic planning skills
- 2 - 4 Years of experience as Regulatory Affairs Manager in Medicated Cosmetic Companies
