The South African Health Products Regulatory Authority (SAHPRA), is the National Medicines Regulatory Authority established in terms of the Medicines and Related Substances Act, 1965, (Act No. 101 of 1965) as amended, to provide for the monitoring, evaluation, regulation, investigation, inspection, registration and control of medicines, scheduled substances,...
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Evaluate and generate evaluation report(s) for registration applications (Generics & New Chemical Entities) in compliance with required template and adopted regulatory /scientific standards (SAHPRA and VICH/EMA technical requirements) and submit for peer review,
Evaluate and generate evaluation report(s) for clinical variation applications (Generics & NCEs) in compliance with required template and adopted regulatory /scientific standards (SAHPRA and VICH/EMA guidelines) and submit for peer review, Provide quality assurance of reports and facilitate resolutions on technical matters, Develop and update guidelines, and templates,
Form part of technical working groups or special projects and provide support to the unit as well as to advisory committees, Adhere to SOPs and guidelines..
Qualification :
Matric certificate and a Bachelor of Veterinary Science degree at NQF Level 8, as recognized by the South African Qualifications Authority (SAQA).
Additionally, candidates must be registered in South Africa to practice as a veterinarian. A postgraduate qualification will be considered an advantage.
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