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) ensuring timeous processing of regulatory applications. Key Responsibilities: Manage work streams for- and report 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
Senior Regulatory Affairs Pharmacist to join our client's team. As a Senior Regulatory Affairs Pharmacist responsible for ensuring compliance with regulatory requirements and managing the registration of pharmaceutical 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 responsible for ensuring compliance with regulatory requirements and managing the registration of pharmaceutical 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 Responsible to ensure that a Pharmaceutical Quality Management System is in place. Responsible for initiating activities, in collaboration with the head of Quality Management. Responsible to ensure that a letter of authorization
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
/>• Provide, Lead, manage, and execute strategic direction as the regulatory affairs pharmacist
•
Ensure and supervise that regulatory documentation meets relevant regulatory requirements and specifications
specifications.
• Provide input to the regulatory strategy in-line with business objectives
• Detailed
Detailed understanding of regulatory guidelines and technical requirements
• Manage and implement safety
safety updates where required
• Manage Chemistry Manufacturing and Controls (CMC / P&A) updates
Regulatory Affairs Scientist Industry: Pharmaceutical Location: JHB Equity Requirement: EE Large Pharmaceutical employ a Regulatory Affairs Scientist. The following applies: Key Responsibilities: Managing and coordinating applications. Managing and coordinating response to the regulatory authority. Maintain regulatory knowledge is required. Effectively managing, auditing and implementation of Regulatory systems Key Requirements: field Minimum 1-2 years' solid experience in Regulatory Affairs, preferably in orthodox, human medicines
pharmaceutical sector has an opportunity for an RA Manager to lead their team of RA pharmacists and RA scientists dossier compilation from you - you will strategically manage the team and ensure output. You need 5 years of step into an RA Manager role, guided by the Head of RA. You MUST have some management or Team Lead experience team to apply. This role is more about project management. Ensure that there are a team achieves their monthly work output targets. Primarily you will be managing the RA team, (but also assisting the team if there
competent, efficient, thorough, and hardworking Regulatory Affairs Specialist. The position requires the candidate and have strong interpersonal skills and time management, organizational and communication skills. This according to ISO 13485 Compliance with medical device regulatory requirements. ● Tertiary degree as per the minimum
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 Responsible to ensure that a Pharmaceutical Quality Management System is in place. Responsible for initiating activities, in collaboration with the head of Quality Management. Responsible to ensure that a letter of authorization