maintaining, and administering corporate hardware systems. Upgrading, installing, and configuring new hardware resolve support issues. Managing the company PABX system and interfacing with the Vendor to procure toner with advancements and best practices in IT administration. Suggesting and implementing improvements in computer science, information technology, information systems, or similar with basic networking knowledge. At best practices in IT administration and system security. Experience with IT systems, networks, Microsoft
projects Implement and manage a Pharmacoviligance system compliant to local health authorities and the Company's warehouse and distributors or implement quality systems to ensure quality products Ensure that all Manufacturers in place Conduct external audits to ensure that systems are in place to maintain the positive GMP status phases of the product, in-process, release and shelf life and analytical methods if required and confirm that that our products are stable throughout the shelf life Ensure that Product Quality Reviews are available
projects Implement and manage a Pharmacoviligance system compliant to local health authorities and the Company's warehouse and distributors or implement quality systems to ensure quality products Ensure that all Manufacturers in place Conduct external audits to ensure that systems are in place to maintain the positive GMP status phases of the product, in-process, release and shelf life and analytical methods if required and confirm that that our products are stable throughout the shelf life Ensure that Product Quality Reviews are available
and enhance the South Africa Quality Management System to be SAHPRA inspection-ready at all times and of products, and confirm that they have quality systems in place to ensure high quality products. Ensure as per the GMP Audit Schedule, to ensure that systems are in place to maintain the positive GMP status Change Control software system (Veeva Electronic Document Management System). Coordinate monthly Change products are stable throughout the approved shelf life. Ensure that analytical methods are validated as
and enhance the South Africa Quality Management System to be SAHPRA inspection-ready at all times and of products, and confirm that they have quality systems in place to ensure high quality products. Ensure as per the GMP Audit Schedule, to ensure that systems are in place to maintain the positive GMP status Change Control software system (Veeva Electronic Document Management System). Coordinate monthly Change products are stable throughout the approved shelf life. Ensure that analytical methods are validated as
technicians, Procurement managers and hospital administrators. Meeting (and exceeding) sales targets for national territory using available systems, which includes daily administrative duties (logging calls, corporate codes, regulatory directive and guidelines, as applicable to the role, and to the program for legal compliance Representatives Administrative Staff External: Radiologists Radiographers Administrative Support Staff Candidates that meet the criteria may submit their applications via this portal or via vacancy link on www.mnarecruitment
technicians, Procurement managers and hospital administrators. Meeting (and exceeding) sales targets for national territory using available systems, which includes daily administrative duties (logging calls, corporate codes, regulatory directive and guidelines, as applicable to the role, and to the program for legal compliance Representatives Administrative Staff External: Radiologists Radiographers Administrative Support Staff Candidates that meet the criteria may submit their applications via this portal or via vacancy link on www.mnarecruitment
are: Responsible Pharmacist Duties as per latest applicable legislation: Responsible for the continuous supervision ensure that a Pharmaceutical Quality Management System is in place. Responsible for initiating and coordinating could amount to a contravention of legislation applicable to the pharmacy business, is introduced or carried registering new products and line extensions and their life cycle management. Develop strong partnerships within intelligence activities and determine the impact of applicable intelligence on the company Qualifying Requirements
are: Responsible Pharmacist Duties as per latest applicable legislation: Responsible for the continuous supervision ensure that a Pharmaceutical Quality Management System is in place. Responsible for initiating and coordinating could amount to a contravention of legislation applicable to the pharmacy business, is introduced or carried registering new products and line extensions and their life cycle management. Develop strong partnerships within intelligence activities and determine the impact of applicable intelligence on the company Qualifying Requirements
stand in RP in the absence of the RP. Quality systems/SOPs drafting, training, maintaining and distribution distribution. Product Release (based on Applicant release) Audits (preparation and correcting any non-conformances Assessments. To implement and train on Quality systems, SOPs and GDP Pharmacovigilance reporting. Fine Lot status updates in the Warehouse Management System. Ensuring that weekly housekeeping checks are done environment. Experience in Quality Management Systems would be an advantage Oracle R12 experience would