descripción del trabajo

Global Responsibility Schedule and supervise the manufacturing plan and control the manufacturing processes on a production line on each shift, ensuring that volume, quality and cost targets are achieved and coordinating with Planning, Logistics, Warehouse, Maintenance and Quality Assurance on the work performed. Specific Responsibilities Supervise the production schedule and control the manufacturing processes in each shift and the correct operation of the equipment, resolving and making decisions on the impact of the manufacturing processes, in order to meet the plan on time and comply with the established quality specifications. Propose the manufacturing schedule according to the capacity of the planned manufacturing lines to optimize the productivity of the lines in the area. Organize the available personnel resources and make the necessary changes according to the evolution of the manufacturing plan in order to optimize the performance of all the equipment in the area and avoid line stoppages. Investigate incidents, deviations and OOS (Out Of Specifications) analytical findings produced in the equipment and processes of the area and notify them to Quality Assurance for batch release; and take the appropriate decisions to solve them and continue the process.Propose improvements to the operation, equipment and facilities. Communicate, coordinate and monitor equipment breakdowns in the area with both internal personnel and external maintenance providers to resolve the problem. Develop the manufacturing process and manufacturing equipment, establishing critical parameters and their ranges for the introduction of new products as well as improvements. Review work procedures related to manufacturing equipment and production processes, as well as coordinate and train personnel in the equipment area for their correct use. Perform audits to customers with Quality Assurance to defend the quality system of the area. Advise for the realization of new projects in the area and direct the implementation of new processes until they are put into production. Organize and supervise the generation of manufacturing documentation and deliver it to Quality Assurance for batch approval. Validate the documentation review processes in the area. Requirements and personal skills Education: Degree in Natural Sciences/Engineering or Technical Engineer. Master's Degree in Pharmaceutical Industry highly valued. Languages: Spanish essential. Advanced English. Experience (years/area): +4 years of experience in people management positions in production in the pharmaceutical sector. Specific knowledge: Industrial management Travels: Open to travel occasionally. Personal skills: Ability to work both in a team and autonomously, dynamism and multitasking, ability to work under pressure (tight deadlines) and to solve problems.