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Job Summary: A professional to manage production processes, ensuring compliance with GMP, developing teams, and optimizing quality, productivity, and costs. Key Highlights: 1. Management of production processes and compliance with GMP standards. 2. Leadership and team development. 3. Focus on operational excellence, quality, and productivity. Description: * Bachelor's degree in Pharmacy, Production Engineering, Administration, or related fields. * A bachelor's degree in Pharmacy will be considered a plus. * Postgraduate studies/MBA in Quality, Productivity, Pharmaceutical Industrial Management, or related fields are desirable. * Proficiency in Microsoft Office. * Ensure production processes are conducted in accordance with GMP and applicable legislation through documentation control and process monitoring. * Provide information and develop plans to support production planning by establishing daily, weekly, and monthly schedules, meeting qualitative and quantitative production mix delivery requirements. * Manage, train, and develop employees to achieve company objectives through indicator monitoring against pre-established targets and appropriate headcount sizing and task allocation. * Ensure proper use of equipment and physical infrastructure by employees through inspections and daily activity monitoring, overseeing corrective maintenance execution and jointly planning preventive maintenance with Maintenance and PCP departments. * Participate in the selection process for employees reporting to this position. * Monitor cost center expenses under management, evaluating budgeted vs. actual expenditures, proposing improvements and conscious utilization of available resources to meet monthly and annual budget targets. * Respond to sanitary inspections and internal audits by implementing action plans, improving documentation, and collaborating with the production base. * Drive process improvements through operational excellence studies and projects, focusing on quality, productivity, and cost efficiency. * Assess production feasibility during new product launches based on existing resources and define conditions for execution. * Perform all activities in compliance with safety, hygiene, and Good Manufacturing Practices (GMP), in coordination with responsible departments to ensure adherence to established standards. * Participate in Change Control Committees, conducting evaluations and allocating resources to support process improvements and modifications as required by the company. * Analyze and prepare technical specifications (ERU) for procurement of new equipment and physical layout design for proposed new areas. 2512040202181460293
