Ref 6511. One of our clients in the pharmaceutical manufacturing arena has an exciting opportunity for an experienced RA Manager.
Duties include proactively monitoring, reviewing, interpreting and translating all national Regulatory requirements of the Medicine Regulatory Authority (MRA), as well as implementing strategies for the earliest possible Regulatory approvals to support business.
Candidates must have a thorough understanding of Laws and Regulations governing the registration of medicines in the SADAC countries.
Additional requirements for the position are 5 years Regulatory Affairs experience and 2 years management experience as well as a B.Pharm degree.
If you meet our client’s requirements and would like to apply for this position, please email a copy of your CV to email@example.com and if you do not hear from us within 2 weeks, please consider your application unsuccessful.