As a Senior Regulatory Affairs and Compliance Specialist, you will play a crucial role in overseeing
overseeing regulatory submissions, ensuring compliance with all applicable laws and regulations, and providing
providing expert guidance on regulatory matters.
Duties and responsibilities include:
Responsibilities Understand and apply all relevant regulatory/statutory requirements such as the FIC Act, FICA central database including engagement letters and compliance memos accordingly Responsible for linking client
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Responsibilities Understand and apply all relevant regulatory/statutory requirements such as the FIC Act, FICA central database including engagement letters and compliance memos accordingly Responsible for linking client
Senior Regulatory Pharmacist. Job Purpose: Support the Regulatory team to provide superior Regulatory services To ensure legal and regulatory compliance with the relevant medicine Regulatory Authorities (Country Pharmacy Council, ensuring timeous processing of regulatory applications. Key Responsibilities: Manage work stakeholders Establish regulatory priorities and allocate resources and workloads Review regulatory agency submission timelines, accuracy, comprehensiveness, or compliance with regulatory standards Co-ordination and submission
Senior Regulatory Affairs Pharmacist Industry: Pharmaceutical Location: Midrand Equity Requirement: EE with Regulatory Authorities, internal and external stakeholders Formulate or implement regulatory affairs policies and procedures to ensure that regulatory compliance is maintained or enhanced. Key Requirements: Pharmacy Council 3 to 5 years' experience in Regulatory Affairs, preferably in human medicines Demonstrable
Analytics
Regulatory Affairs Manager Industry: Pharmaceutical Location: JHB Equity Requirement: EE Lead the Regulatory Regulatory team and to ensure legal compliance with the relevant medicine Regulatory Authorities (Country Specific Pharmacy Council, ensuring timeous processing of regulatory applications. Key Responsibilities: Manage work other MRA's and third-party stakeholders Review regulatory agency submission of materials to ensure timelines timelines, accuracy, comprehensiveness, or compliance with regulatory standards Co-ordination and submission
Regulatory Affairs Scientist Industry: Pharmaceutical Location: JHB Equity Requirement: EE Large Pharmaceutical Pharmaceutical Manufacturing facility seeks to employ a Regulatory Affairs Scientist. The following applies: Key coordinating response to the regulatory authority. Maintain regulatory knowledge of the various territories Effectively managing, auditing and implementation of Regulatory systems Key Requirements: BSc or equivalent Science field Minimum 1-2 years' solid experience in Regulatory Affairs, preferably in orthodox, human medicines
looking for a Regulatory Affairs/Quality Assurance Pharmacist to join their team. Regulatory Affairs (RA): and approve artwork and promotional material in compliance with legislation; submit to authorities as needed