JOB SUMMARYTo ensure all registration and documentation are up to date.CompanyOur client is an indigenous pharmaceutical company.Objectives
Planning and coordination of submission of product registration applications and follow through the application during the evaluation phase to achieve approval in line with planned registrations.
To ensure that documents for new registration and re-registration are obtained to ensure submission is achieved by due dates.
To ensure that submissions for license renewal are done JIT before license expiry so as to achieve approvals and to avoid top line impact due to license expiry.
To enhance and facilitate approval of new products and re-registration of already approved products as at when due
BACKGROUND
First degree in pharmaceutical.
As the ideal candidate you will have at least 3 years minimum of experience of working in a Regulatory Affairs role within an EU Medical Devices company.
Technical competence and good problem solving and analytical skills.
Ability to communicate effectively.
Interested candidate should forward their CV to semm@bestsearchrecruitment.com
Apply via :
semm@bestsearchrecruitment.com
