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Job Summary: A professional to manage production processes, teams, and ensure compliance with regulations, optimizing quality, productivity, and costs in the industry. Key Highlights: 1. Management of production processes and compliance with GMP and current legislation. 2. Leadership and team development, monitoring KPIs and targets. 3. Optimization of processes and costs, with a focus on operational excellence. Description: * Bachelor's degree in Pharmacy, Production Engineering, Business Administration, or related fields. * A bachelor's degree in Pharmacy will be considered a plus. * Postgraduate degree/MBA in Quality, Productivity, Pharmaceutical Industrial Management, or related fields is desirable. * Proficiency in Microsoft Office. * Ensure production processes are carried out in accordance with GMP and current legislation through documentation control and process monitoring. * Provide information and develop plans to support production planning, via daily, weekly, and monthly scheduling, ensuring delivery of both qualitative and quantitative production mixes. * Manage, train, and develop employees to achieve company objectives, through monitoring KPIs 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 who will report to this position. * Monitor cost center expenses under management, conducting evaluations of budgeted versus actual expenditures, proposing improvements and conscious utilization of available resources to meet monthly and annual budget requirements. * Respond to sanitary inspections and internal audits, implementing action plans, improving documentation, and coordinating with production staff. * Ensure process improvements through studies and operational excellence projects, focusing on quality, productivity, and costs. * Analyze production feasibility during product launches based on existing resources and define conditions for execution. * Perform all activities in compliance with safety, hygiene, and Good Manufacturing Practice (GMP) standards, in coordination with responsible departments to ensure adherence to established standards. * Participate in Change Control Committees, performing assessments and allocating resources for process improvements and modifications as required by the company. * Analyze and prepare technical specifications (URS) for procurement of new equipment and physical layout of proposed new areas. 2512040202181460293
