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Main Purpose of Job: Responsible for activities which lead to and maintain regulatory approval to market devices. Works with various stakeholders such as labeling / global team for launch readiness. Develops and implements strategies for earliest possible approvals. Ensures timely preparation of submissions. Builds rapport with regulatory agencies. Anticipates regulatory environment change and manages the regulatory intelligence... • Diploma, Advanced/Higher/Graduate Diploma, Bachelor’s degree or equivalent, preferrably in pharmacy, health sciences or related science background Skills and Experience: • 2 years experience in Medical Device Regulatory Affairs preferred. • Proficient in Microsoft Office applications especially excel files. • Effective interpersonal, communication and analytical skills • Proficiency in written and spoken English and Local language. • Independent. Highly result...