dossier

About the RoleOur client is seeking a skilled and precise Medical Writer to craft essential documentation for regulatory submissions from their remote work environment, supporting their teams near Mahikeng . This role is critical for translating complex scientific and clinical data into clear, concise, and compliant regulatory documents required for drug...

About the Role Our client is seeking a skilled and precise Medical Writer to craft essential documentation for regulatory submissions from their remote work environment, supporting their teams near Mahikeng. This role is critical for translating complex scientific and clinical data into clear, concise, and compliant regulatory documents required for drug...

Le CTA Riviera, centre spécialisé dans les troubles des apprentissages, recherche un(e) Employé(e) de commerce, Assistant(e) médical(e) ou Secrétaire médical(e) pour rejoindre son équipe professionnelle et dévouée.Entrée en fonction : de suite ou à convenir. Vous assurerez l'accueil des patients, la gestion des rendez-vous et l'administration du...

Le CTA Riviera, centre spécialisé dans les troubles des apprentissages, recherche un(e) Employé(e) de commerce, Assistant(e) médical(e) ou Secrétaire médical(e) pour rejoindre son équipe professionnelle et dévouée. Entrée en fonction : de suite ou à convenir. Vous assurerez l'accueil des patients, la gestion des rendez-vous et l'administration...

Youforce zoekt een senior payroll specialist die verantwoordelijk is voor het volledige salarisadministratieproces voor complexe klantdossiers en die wet- en regelgeving vertaalt naar feilloze payroll.Je fungeert als trusted advisor voor klanten en collega’s, coacht junior en medior collega's en werkt in een hybride setting tussen kantoor in Amersfoort en...

About the RoleOur client is seeking a skilled and precise Medical Writer to craft essential documentation for regulatory submissions from their remote work environment, supporting their teams near Mahikeng . This role is critical for translating complex scientific and clinical data into clear, concise, and compliant regulatory documents required for drug...

OttoBauthentic in Johannesburg seeks a strategic Regulatory Affairs Manager to lead regulatory, quality assurance, and pharmacovigilance across operations. You will drive dossier lifecycle management, ensure compliance with SAHPRA, and foster strong relationships with regulatory authorities and internal stakeholders.The role requires a strong track record in...

Placements24 is seeking a knowledgeable Pharmaceutical Regulatory Affairs Specialist to join our expanding team in Pretoria. You will ensure compliance of our pharmaceutical products with SAHPRA, FDA, and EMA standards, manage regulatory dossiers, and liaise with health authorities remotely from Gauteng or beyond.You will monitor regulatory changes, support...

Austell Pharmaceuticals is seeking an experienced Senior Regulatory Affairs Pharmacist to join our Regulatory Affairs team. This role leads regulatory activities across our portfolio, ensuring ongoing SA regulatory compliance and lifecycle management. You will mentor the regulatory team and engage stakeholders to support business growth.The ideal candidate...

Placements24 is seeking a skilled Medical Writer to craft regulatory documentation for submissions from a remote work environment near Mahikeng. You will translate complex clinical data into clear, compliant dossiers and collaborate with medical, clinical, and regulatory teams to ensure accuracy and completeness. The role demands exceptional writing, deep...

Placements24 is seeking a meticulous Regulatory Affairs Specialist to join our established team in a fully remote role. You will monitor regulatory changes, prepare submission dossiers, and liaise with regulatory authorities to secure and maintain product approvals.The ideal candidate will have a strong understanding of regulatory landscapes and a proven...

Placements24 is seeking a skilled Medical Writer to craft regulatory documentation for submissions from a remote work environment near Mahikeng. You will translate complex clinical data into clear, compliant dossiers and collaborate with medical, clinical, and regulatory teams to ensure accuracy and completeness.The role demands exceptional writing, deep...

Placements24 in Pretoria is seeking a seasoned Senior Regulatory Affairs Specialist to join our dedicated team. You will manage regulatory dossiers and oversee submissions to health authorities, ensuring global regulatory compliance.You will collaborate with R&D, manufacturing, and legal to develop regulatory strategies and respond to queries during reviews....

Senior Regulatory Affairs PharmacistREF: MVG/SRAA high-impact opportunity for an experienced Regulatory Affairs Pharmacist to step into a role focused on strengthening long-term regulatory leadership within a dynamic pharmaceutical environment.The ideal candidate brings end‑to‑end regulatory lifecycle expertise, including Compliance, Labelling, dossier...

About the Role Our client is seeking a knowledgeable and proactive Pharmaceutical Regulatory Affairs Specialist to join their expanding team. This role, based in Pretoria , is essential for ensuring that all our client's pharmaceutical products comply with national and international regulatory requirements. You will be responsible for preparing and...

About the Role Our client is seeking a highly organized and knowledgeable Regulatory Affairs Specialist to join their team, supporting operations from Richards Bay. This role is critical in ensuring that all pharmaceutical products meet the necessary regulatory requirements for marketing and distribution in various target markets. You will be responsible for...

About the Role Our client is seeking a meticulous and experienced Senior Regulatory Affairs Specialist to enhance their regulatory compliance efforts in Vereeniging. This vital role involves navigating the complex regulatory landscape to ensure that pharmaceutical products meet all local and international standards for marketing authorization and continued...

Key purpose: To fulfill the position as regulatory affairs pharmacist for the company and any division within the group. Duties and responsibilities: Responsible for new product applications. Compilation and submission of Post Registration amendments to ensure dossier compliance. Responsible for pre and post registration SAHPRA...

About the RoleOur client is looking for a knowledgeable Regulatory Affairs Specialist to join their compliance team in Queenstown . This role is vital for ensuring that all pharmaceutical products meet the necessary regulatory requirements for marketing and distribution within South Africa and potentially international markets. You will be responsible for...

About the RoleOur client, a dynamic pharmaceutical company with a strong pipeline, is looking for a proactive Regulatory Affairs Specialist to join their team in Stellenbosch . This role is pivotal in ensuring that all drug products meet the required regulatory standards for approval and marketing in various jurisdictions. You will be responsible for...