Knowledge of quality and regulatory compliance: SAPHRA, WHO, and GDP, and IP management Technology transfer WHO) and GLP guidelines Experience with in local quality audits will be an advantage Exposure to pharmaceutical pharmaceutical product development and commercialization Manage laboratory administration, including budgeting operations Maintain compliance with cGMP guidelines and manage change controls and NCRs Address facility issues improvement, and quality risk management Manage deviations, change controls, and CAPAs Drive quality objectives
Knowledge of quality and regulatory compliance: SAPHRA, WHO, and GDP, and IP management Technology transfer WHO) and GLP guidelines Experience with in local quality audits will be an advantage Exposure to pharmaceutical pharmaceutical product development and commercialization Manage laboratory administration, including budgeting operations Maintain compliance with cGMP guidelines and manage change controls and NCRs Address facility issues improvement, and quality risk management Manage deviations, change controls, and CAPAs Drive quality objectives
Responsibilities: Managing and coordinating the compilation and submission of new product applications. Managing and registration process is required. Effectively managing, auditing and implementation of Regulatory systems pharmaceutical industry. Key Competencies Sound project management skills Strategic thinking and planning Ability
Responsibilities: Managing and coordinating the compilation and submission of new product applications. Managing and registration process is required. Effectively managing, auditing and implementation of Regulatory systems pharmaceutical industry. Key Competencies Sound project management skills Strategic thinking and planning Ability