orientated Customs Affairs Clerk – Junior based at our Customs division in Durban. Processing of customs and statutory body documents required for customs Audit products against customs and other statutory body requirements Harmonised Customs Tariff and related books Comply with the requirements of the quality management system as required Attending to Customs/SAPS,etc stops Acquittals Visiting Customs if and when required Attending Stop report General Customs adjustments, VOC'S Experience 3- 5 years import/customs experience in the Clearing
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) and experience regarding QA processes, APQRs, customer complaints, etc. In-depth knowledge of Regulations
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) and experience regarding QA processes, APQRs, customer complaints, etc. In-depth knowledge of Regulations
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
Provision of a reliable and efficient regulatory affairs service that puts current regulatory and compliance
/>• 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