Senior Regulatory Affairs Pharmacist to join our client's team. As a Senior Regulatory Affairs Pharmacist will be responsible for ensuring compliance with regulatory requirements and managing the registration of products. Responsibilities Prepare and submit regulatory applications for the registration of pharmaceutical pharmaceutical products Review and analyze regulatory documentation for accuracy and completeness Develop and maintain relationships with regulatory authorities Stay updated on changes in regulatory requirements and guidelines
Senior Regulatory Affairs Pharmacist to join our client's team. As a Senior Regulatory Affairs Pharmacist will be responsible for ensuring compliance with regulatory requirements and managing the registration of products. Responsibilities Prepare and submit regulatory applications for the registration of pharmaceutical pharmaceutical products Review and analyze regulatory documentation for accuracy and completeness Develop and maintain relationships with regulatory authorities Stay updated on changes in regulatory requirements and guidelines
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
reliable and efficient regulatory affairs service that puts current regulatory and compliance knowledge operational requirements and internationally accepted regulatory standards and those accepted by the SAHPRA. Bachelor's industry in a manufacturing/quality assurance/regulatory environment. Understanding of a pharmaceutical
direction as the regulatory affairs pharmacist
• Ensure and supervise that regulatory documentation
relevant regulatory requirements and specifications.
• Provide input to the regulatory strategy
business objectives
• Detailed understanding of regulatory guidelines and technical requirements
•
Managing and maintaining regulatory documentation filing system.
• Ensuring regulatory compliance and quality
local staff
• Answering of requests from the Regulatory Authority with co-operation with Global Safety
MINIMUM
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
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