A minimum of 8 years of pharmaceutical regulatory experience is a prerequisite with excellent knowledge
in 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
team. This role will predominantly support the Head of Legal, Risk and Compliance and the CFO within Strate
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
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 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 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
PE000998-CP-1 Our client is looking for an experienced Regulatory and Quality Assurance Pharmacist to join their experience Vet industry experience Knowledge of regulatory submissions in Botswana, Nambia, Zambia, Zimbabwe Job Duties Regulatory Affairs Duties Regulatory Submissions: Prepare and submit regulatory documents to comply with regulatory guidelines and requirements. Compliance: Monitor and interpret regulatory requirements registration of existing products. Coordinate with regulatory bodies for product approvals. Labeling and Advertising:
/>Vet industry experience
Knowledge of regulatory submissions in Botswana, Nambia, Zambia, Zimbabwe
Duties
Regulatory Affairs Duties
Regulatory Affairs Pharmacist (POS24192)
Area; Aeroton
Salary R750 800k
Purpose the role:
Support the Regulatory team to provide superior Regulatory services to relevant departments portfolio outputs. To ensure legal compliance with the relevant medicine Regulatory Authorities (Country Specific Pharmacy Council, ensuring timeous processing of regulatory applications.
Qualifications &
Pharmacy Council
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Regulatory Affairs Manager (POS24277)