years' experience in Regulatory Affairs, preferably in human medicines - Demonstrable experience across deliver to quality, time and cost standards - Experience in use of CTD software builder and compilation
years' experience in Regulatory Affairs, preferably in human medicines - Demonstrable experience across deliver to quality, time and cost standards - Experience in use of CTD software builder and compilation
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Must have working experience in fragrance development and application. Experience in managing raw material
EXPERIENCE REQUIRED
EXPERIENCE REQUIRED
responsibilities. Implement a Stability Master Plan. Experience in Medical Devices 2. COMPLAINTS To ensure that Bilingual: English and Afrikaans. EXPERIENCE REQUIRED Minimum 5 Years QA experience. SOP and master QA document
responsibilities. Implement a Stability Master Plan. Experience in Medical Devices 2. COMPLAINTS To ensure that Bilingual: English and Afrikaans. EXPERIENCE REQUIRED Minimum 5 Years QA experience. SOP and master QA document
Matric/Grade 12 Basic Microbiology Minimum Experience 3-5 years of experience in the laboratory / medical device