Duties and Responsibilities

• Ensure that all company products and services comply with relevant regulatory requirements and standards.

• Stay up-to-date with changes in regulations, guidelines, and industry standards, and communicate these changes to the relevant departments.

• Prepare, review, and submit regulatory documents and applications to relevant regulatory bodies.

• Maintain accurate and up-to-date records of all regulatory submissions, approvals, and correspondence.

• Collaborate with product development teams to provide regulatory guidance throughout the product lifecycle.

• Act as the primary contact with regulatory authorities

• Communicate effectively with internal and external stakeholders to ensure alignment on regulatory requirements and expectations.

• Support the development and implementation of regulatory strategies for new and existing products.

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

• Assist the procurement and logistics manager in the tasks related to EFDA to acquire a pre-import permit

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

Job Requirements

• BSc Degree in Pharmacy or Biomedical Engineering

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

• 1-2 years of service in regulatory affairs is a plus.

• Proficiency in English & Amharic

How to Apply

Interested and qualified applicants can apply online using THIS LINK