Reference: CPT000390-CH-1 The QA Manager and Deputy Responsible Pharmacist will manage, maintain and enhance the South Africa Quality Management System to be SAHPRA inspection-ready at all times and assume all the responsibilities information. Support Supply Chain team to ensure the timely release of quality products into the market. Ensure 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
Reference: CPT000390-CH-1 The QA Manager and Deputy Responsible Pharmacist will manage, maintain and enhance the South Africa Quality Management System to be SAHPRA inspection-ready at all times and assume all the responsibilities information. Support Supply Chain team to ensure the timely release of quality products into the market. Ensure 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
Assist on artwork and related projects Implement and manage a Pharmacoviligance system compliant to local health 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 COA's are in line with the products specifications Manage and role out stability programs per product, per
Assist on artwork and related projects Implement and manage a Pharmacoviligance system compliant to local health 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 COA's are in line with the products specifications Manage and role out stability programs per product, per
external Partners and Principals, and to control and manage a portfolio of product outputs. To ensure legal regulatory applications. Key Responsibilities: Manage work streams for- and report on the assigned portfolio Sound project management capabilities Proven ability to consistently deliver to quality, time and cost standards builder and compilation of eCTD applications. IT skills Ability to prioritise and work to tight deadlines Systems and operations analysis Basic cost management skills Active learning Strategic thinking Ability
queries from relevant departments Effectively managing activity within Regulatory, QA and administrative experience with MS Office, Document Management System and / or Quality Management Systems. Competencies: Attention detail IT skills, document management skills Project management skills Good language skills Ability to tight deadlines Systems approach Cross Functional skills: Ability to network, liaise and negotiate with monitor progress Problem solving and decision-making skills Candidates that meet the criteria may submit their