Regulatory Affairs, preferably in orthodox, human medicines Demonstrable experience across the product development
Regulatory Affairs, preferably in orthodox, human medicines Demonstrable experience across the product development
postgraduate qualification in reasonable time; Oral comprehension and oral expression; Appropriate language skills;
postgraduate qualification in reasonable time; Oral comprehension and oral expression; Appropriate language skills;
enable efficient and effective registration of medicinal products consistent with the supported regions' Experience in regulatory affairs, preferably in human medicines - minimum 8 years of experience. Key Knowledge
maintenance Must possess excellent communication (oral and written), organizational and interpersonal skills
skills. Strong communication skills (written and oral). Ability to work well within a team and also independently
with the relevant Health Regulatory Authorities, Medicines, and Related Substances Control Act 101 of 1965
with the relevant Health Regulatory Authorities, Medicines, and Related Substances Control Act 101 of 1965
with the relevant Health Regulatory Authorities, Medicines, and Related Substances Control Act 101 of 1965