industry is seeking the expertise of a Corporate Affairs Manager to join their team in JHB West. The role will Include
Regulatory Affairs Manager Industry: Pharmaceutical Location: JHB Equity Requirement: EE Lead the Regulatory regulatory applications. Key Responsibilities: Manage work streams for- and report on the assigned group new products Formulate or implement regulatory affairs systems, policies and procedures to ensure that Council Minimum of 5 years' experience in Regulatory Affairs, preferably in human medicines. Demonstrated experience application will be an advantage. Sound project management capabilities Proven ability to consistently deliver
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
Senior Regulatory Affairs Pharmacist to join our client's team. As a Senior Regulatory Affairs Pharmacist, ensuring compliance with regulatory requirements and managing the registration of pharmaceutical products. Responsibilities Participate in regulatory audits and inspections Manage the maintenance and renewal of product registrations (SAPC) Minimum 5 years' experience in Regulatory Affairs (must have experience with human medicine and biologicals) related to dossier submissions and lifecycle management Knowledge of the Marketing Code Systems knowledge
Senior Regulatory Affairs Pharmacist to join our client's team. As a Senior Regulatory Affairs Pharmacist, ensuring compliance with regulatory requirements and managing the registration of pharmaceutical products. Responsibilities Participate in regulatory audits and inspections Manage the maintenance and renewal of product registrations (SAPC) Minimum 5 years' experience in Regulatory Affairs (must have experience with human medicine and biologicals) related to dossier submissions and lifecycle management Knowledge of the Marketing Code Systems knowledge
company has a vacancy for a Head of Regulatory Affairs and Responsible Pharmacist. Job Purpose: To describe 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 any non-compliance with the Pharmacy Act to the management of such pharmacy business and to furnish the Responsible to ensure that no instruction or order of management with regard to the pharmacy business that could
DEPARTMENT OF STUDENT AFFAIRS DEPUTY DIRECTOR: STUDENT AFFAIRS PEROMNES POST LEVEL 4 The successful candidates' heads; Oversee, manage, and provide strategic leadership to unit heads and staff; Manage the monitoring within the department; Operational management: Overall management of operational functions for the department; programmes; Project management; Human Resources and Financial management: Manage Human Resources and eight years' experience, with three years in management, in: Higher Education, as an academic, or professional
/>• Provide, Lead, manage, and execute strategic direction as the regulatory affairs pharmacist
•
requirements
• Manage and implement safety updates where required
• Manage Chemistry Manufacturing
developing of SOP in line with Global SOP’s
• Manage internal and external audits (i.e.Global &
current legislation
• Manage of product complaints and deviations
• Managing and maintaining regulatory
/>o Minimum 5 years’ experience in Regulatory Affairs – (must have human medicine experience and biologicals)
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 compilation and submission of new product applications. Managing and coordinating response to the regulatory authority registration process is required. Effectively managing, auditing and implementation of Regulatory systems Minimum 1-2 years' solid experience in Regulatory Affairs, preferably in orthodox, human medicines Demonstrable
company in the mining industry, is seeking a Community Liaison Officer to join their team in Limpopo Assist beneficiaries in project proposals for SED management evaluation Provide feedback on rejected or approved and within budget Report progress to supervisor/manager Monitor progress of all projects Requirements: Economic Development. 2 years' experience in community development programme. 2 years' experience in