Degree or diploma in Management and/or Regulatory Affairs and Pharmacy,
5 years' experience in Regulatory Affairs in the pharmaceutical industry is an added advantage
DUTIES AND RESPONSIBILITES
Ensure all the product registrations are aligned and up to date available according to the organizational requirements
Communicate with foreign suppliers / internal staff to obtain required documents for registrations S renewals
Ensure all the NMRA approvals, files and documents are according to organizational requirements and standards
Responsible for maintaining accurate documentation and filing of records as well as ISO documents of the Supply Chain Department
QUALIFICATIONS AND REQUIREMENTS
Degree or diploma in Management and/or Regulatory Affairs and Pharmacy
5 years' experience in Regulatory Affairs in the pharmaceutical industry is an added advantage
Having a pharmacist license will be a further added advantage Good communication and interpersonal skills
A dynamic self-driven, well organized, motivated individual