Job Vacancy Details
Pharmaceutical
Gauteng
Permanent
Updated May 9, 2012
The responsibilities of this role involves liaising with the manufacturers of ARV's, Medicines Control Council during the regulatory process, handling of complex quality issues in order to satisfy Sales and Marketing, Health Care Practitioners (HCP) and other customers within the market. You would be required to liaise and advise regulatory and packaging development personnel at the various locations on issues arising or any amendments required for labelling of products. An integral part of the role involves ensuring the registration of organisations products and maintenance of dossiers. You would be required to complete functional reporting regularly.
Who we're looking for
- B Pharm and registration with the South African Pharmacy council
- Minimum of three years experience within regulatory affairs
- Attention to detail is essential
- Established relationships with key role players in industry would be advantageous
- A motivated individual who keen business sense
About our client
Since their inception over five years ago, my client has aggressively taken the South African market by storm. They have launched over 10 products to date, half of which have been locally manufactured. They place much emphasis on maintaining a productive environment where creativity is encouraged.
What's on offer
An outstanding offer
Michael Page Contact
For further info, apply or phone on +27 (0)11 303 8300.
Job Ref: 6458
Your application will be sent to Anneline Govender.
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