pharmaceutical company has a vacancy for a Head of Regulatory Affairs and Responsible Pharmacist. Job Purpose: medicines with the South African Health Products Regulatory Authority and the maintenance of these registrations accountable to the South African Health Products Regulatory Authority and the South African Pharmacy Council Quality Assurance/ Pharmacovigilance/ Medical Affairs. Ensure the availability of training plans according completed according to the training plan. Head of Regulatory Affairs Duties: Ensuring alignment of global and
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 accuracy, comprehensiveness, or compliance with regulatory standards Co-ordination and submission of new
A minimum of 8 years of pharmaceutical regulatory experience is a prerequisite with excellent knowledge
ensure legal compliance with the relevant Health Regulatory Authorities (Country Specific where applicable
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
Regulatory Affairs Manager Industry: Pharmaceutical Location: JHB Equity Requirement: EE Lead the Regulatory ensure legal compliance with the relevant medicine Regulatory Authorities (Country Specific where applicable) 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 accuracy, comprehensiveness, or compliance with regulatory standards Co-ordination and submission of new
Regulatory Affairs Scientist Industry: Pharmaceutical Location: JHB Equity Requirement: EE Large Pharmaceutical Manufacturing facility seeks to employ a Regulatory Affairs Scientist. The following applies: Key Responsibilities: 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
required. A minimum of 8 years of pharmaceutical regulatory experience is a prerequisite with excellent knowledge ensure legal compliance with the relevant Health Regulatory Authorities (Country Specific where applicable relevant regulations in Africa. Experience with regulatory authorities in sub-Saharan Africa and French will be advantageous Significant experience of regulatory drug development, manufacture, commercialisation commercialisation or equivalent. Knowledge of regulatory procedures and legislation for drug development, product
a Head of Regulatory position. Job Purpose: Provides strategic and operational regulatory leadership of current local and global Regulatory trends to identify future regulatory requirements and strategies strategies. Influences Regulatory authorities through regular contacts to improve Regulatory outcomes. Responsible management of a skill group such as CMC, Regulatory affairs project management, etc. Responsible for Provides effective lobbying and influencing on regulatory agencies and trade associations on product and
pharmaceutical company has a vacancy for a Head of Regulatory Affairs and Responsible Pharmacist. Job Purpose: medicines with the South African Health Products Regulatory Authority and the maintenance of these registrations accountable to the South African Health Products Regulatory Authority and the South African Pharmacy Council Quality Assurance/ Pharmacovigilance/ Medical Affairs. Ensure the availability of training plans according completed according to the training plan. Head of Regulatory Affairs Duties: Ensuring alignment of global and
A long-established leader in the pharmaceutical sector has an opportunity for an RA Manager to lead their team of RA pharmacists and RA scientists - about 4 to 8 people in the team. The position requires no dossier compilation from you - you will strategically manage the team and ensure output. You
An established leader in the pharmaceutical sector has an opportunity for an RA Pharmacist with at least 2 to 4 years of solid RA dossier compilation experience. Experience using Extedo, or docuBridge, or a similar electronic dossier compiling platform is preferred. Experience in RA for CAMS / Compl