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:
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
A minimum of 8 years of pharmaceutical regulatory experience is a prerequisite with excellent knowledge
Africa.
To ensure legal compliance with the relevant Health Regulatory Authorities (Country Specific
relevant regulations in Africa.
Experience with regulatory authorities in sub-Saharan Africa and French
be advantageous
Significant experience of regulatory drug development, manufacture, commercialisation
commercialisation or equivalent.
Knowledge of regulatory procedures and legislation for drug development, product
required regulatory support. Reviewing artwork relating to products ensuring that it is in compliance with legal requirements. Checking Format and Content Compliance with latest codes of conduct and regulations abreast of developments and changes in the local regulatory environment which directly impacts on the product Council (SAPC) is essential Minimum of 2 years Regulatory Affairs experience in pharmaceutical industry industry . Experience working with SAHPRA and other Regulatory Authorities in Africa. Excellent spoken and written
competent and experienced Regulatory Affairs Scientist for the Regulatory Affairs Department Key Job Compilation and update of documents to be submitted to regulatory authorities, this includes the compilation of to customer (both internal and external) and regulatory authority queries Ensuring that annual product according to internal procedures and in line with regulatory expectations Compilation of process qualification