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
Senior Regulatory Affairs Pharmacist Industry: Pharmaceutical Location: Midrand Equity Requirement: EE with Regulatory Authorities, internal and external stakeholders Formulate or implement regulatory affairs systems, 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
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
looking for a Regulatory Affairs/Quality Assurance Pharmacist to join their team. Regulatory Affairs (RA): Submit registrations according to the renewal cycle. Perform administrative duties, including database maintenance. Quality
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
relationships effectively and provide required regulatory support. Reviewing artwork relating to products 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 . Experience Experience working with SAHPRA and other Regulatory Authorities in Africa. Excellent spoken and written In-depth knowledge of regulatory requirements . Understanding of regulatory compliance and the impact
the compliance of pharmaceutical products with regulatory requirements in South Africa and other designated designated markets. This role involves managing regulatory submissions, writing and reviewing Chemistry, Manufacturing up-to-date knowledge of regulatory guidelines. Key Responsibilities: 1. Regulatory Submissions: Prepare Prepare, compile, and submit regulatory dossiers for new product registrations, renewals, and variations to Products Regulatory Authority (SAHPRA) and other relevant authorities. Manage timelines for regulatory submissions
The company is an established leader in the pharmaceutical sector, with over 90 products, many of them 'famous-brand' and 'Blockbuster' products in the CAMS, cosmetics, and medical devices sector. They export to over 60 countries. In particular, this position will require input into RA requirements
A long-established leader in the pharmaceutical sector has an opportunity for an RA Manager to lead their team. You need 5 years of RA experience in the dossier compilation of registered medicines. The position could suit an ambitious Senior RA Pharmacist too, who is ready to step up into an RA Mana