highly skilled and motivated Senior Regulatory Affairs and Compliance Specialist to join a dynamic team Johannesburg, Gauteng. As a Senior Regulatory Affairs and Compliance Specialist, you will play a crucial crucial role in overseeing regulatory submissions, ensuring compliance with all applicable laws and regulations guidance on regulatory matters. Duties and responsibilities include: Develop and implement regulatory strategies interpret regulatory developments and changes in legislation to ensure ongoing compliance. Act as the
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 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
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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
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: