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 there have been recent changes to registered information. Support Supply Chain team to ensure the timely 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 the South Africa Quality Management System to be SAHPRA inspection-ready at all times and assume all the there have been recent changes to registered information. Support Supply Chain team to ensure the timely 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
departments Effectively managing activity within Regulatory, QA and administrative systems Preparing, reviewing 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
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 reflect the correct information as per the current product dossier and legislation. Manage and maintain the the relevant artwork master files. Manage bar codes and nappi codes QA release products as per the QA
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 reflect the correct information as per the current product dossier and legislation. Manage and maintain the the relevant artwork master files. Manage bar codes and nappi codes QA release products as per the QA
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 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