Reference: CPT000390-CH-1 The QA Manager and Deputy Responsible Pharmacist will manage, maintain and enhance the the South Africa Quality Management System to be SAHPRA inspection-ready at all times and assume all the batches released to market. Quality Management Processes: Manage all final product manufacturers (local Manufacturing Licenses and Site Master Files in place. Manage the local GMP Audit program and conduct external these are maintained as per revision register. Manage the Change Control process and facilitate and capture
external Partners and Principals, and to control and manage a portfolio of product outputs. To ensure legal Responsibilities: Manage work streams for- and report on the assigned portfolio of products: Assisting with internal internal product queries from relevant departments Assisting with external product queries from the SAHPRA commercialization and maintenance lifecycle Sound project management capabilities Proven ability to consistently deliver deadlines Systems and operations analysis Basic cost management skills Active learning Strategic thinking Ability
training Assisting with internal product queries from relevant departments Effectively managing activity experience with MS Office, Document Management System and / or Quality Management Systems. Competencies: Attention Attention to detail IT skills, document management skills Project management skills Good language skills Ability
products are release for sale Assist on the facilitation of change controls Assist on artwork and related projects projects Implement and manage a Pharmacoviligance system compliant to local health authorities and the shortcomings to stakeholders and in the correct format. Manage all Final product manufacturers, Final Release Quality/Technical agreements are in place for all our products Manage and facilitate artwork projects with the different dossier and legislation. Manage and maintain the relevant artwork master files. Manage bar codes and nappi
products are release for sale Assist on the facilitation of change controls Assist on artwork and related projects projects Implement and manage a Pharmacoviligance system compliant to local health authorities and the shortcomings to stakeholders and in the correct format. Manage all Final product manufacturers, Final Release Quality/Technical agreements are in place for all our products Manage and facilitate artwork projects with the different dossier and legislation. Manage and maintain the relevant artwork master files. Manage bar codes and nappi
Reference: CPT000390-CH-1 The QA Manager and Deputy Responsible Pharmacist will manage, maintain and enhance the the South Africa Quality Management System to be SAHPRA inspection-ready at all times and assume all the batches released to market. Quality Management Processes: Manage all final product manufacturers (local Manufacturing Licenses and Site Master Files in place. Manage the local GMP Audit program and conduct external these are maintained as per revision register. Manage the Change Control process and facilitate and capture