Key Responsibilities and Accountabilities :      

• Plan, Organize, coordinate and direct the activities of the unit as per the company’s rules & regulations

• Search new supplier and register their products as per EFDA’s registration guidelines

• Follow up the document evaluation by EFDA

• Submit actual samples to EFDA for laboratory analysis and follow up the results

• Notify suppliers before the expiration of the registration time and re-register the products

• Apply and follow up the status of manufacturers applied for GMP inspection

• Follow up EFDA’s new directives & incorporate with the company procedures

• Follow up the disposal of damaged and expired products on timely basis 

Job Requirements

Academic Qualifications/Experience :

• BSc Degree in Pharmacy or Biomedical Engineering

• 1-2 years’ service as a regulatory affair officer in a similar import setup.

Skills :

• Basic computer application skills, knowledge of registration guidelines and process

• Proficiency in English & Amharic

• Excellent interpersonal communication

How to Apply

Submit your CV via email: delta.reyhumanresources@gmail.com