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Category:
Pharmaceutical
Location:
Employment Type:
Full time
Salary:
Job Description
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
Interested and Qualified Applicants can apply through
[email protected]
