Prepare and submit regulatory documents to health authorities (e.g., FDA, EMA). Ensure that submissions comply Ensure company practices and products comply with national and international regulations. Product Registration: requirements. Communication: Liaise with regulatory authorities and industry groups. Maintain up-to-date knowledge
Prepare and submit regulatory documents to health authorities (e.g., FDA, EMA). Ensure that submissions comply Ensure company practices and products comply with national and international regulations. Product Registration: requirements. Communication: Liaise with regulatory authorities and industry groups. Maintain up-to-date knowledge
and reporting to the respective international authorities Investigate and track other compliance requirements will be beneficial. Strong knowledge of local, national, and international chemical regulations Excellent
update of documents to be submitted to regulatory authorities, this includes compilation of common technical Sciences or equivalent qualification as per the National Qualification Framework (NQF) Experience: Good
update of documents to be submitted to regulatory authorities, this includes compilation of common technical Sciences or equivalent qualification as per the National Qualification Framework (NQF) Experience: Good
(RA): Submit new dossiers for health products to authorities in South Africa and other markets (Namibia, Botswana material in compliance with legislation; submit to authorities as needed. Renew all registrations according assist with GMP in-house training. Act as an authorized representative for medical devices. B. Pharm
(RA): Submit new dossiers for health products to authorities in South Africa and other markets (Namibia, Botswana material in compliance with legislation; submit to authorities as needed. Renew all registrations according assist with GMP in-house training. Act as an authorized representative for medical devices. B. Pharm
vely participate in key global, regional, and national stakeholder fora
compliance with the relevant medicine Regulatory Authorities (Country Specific where applicable), Medicines applications for submission to the regulatory authorities Work in collaboration with internal and external maintain effective relationships with Regulatory Authorities, internal and external stakeholders Formulate
Health Products Regulatory Authority (SAHPRA) and other relevant authorities. Manage timelines for regulatory Communication: Act as the primary contact with regulatory authorities, responding to queries and providing additional