Sterile Production Coordinator
2 days ago
Gijón
An important pharmaceutical laboratory in Madrid is looking to expand its manufacturing team. Requirements Experience minimum 3 years in Leading production teams in sterile areas to ensure that all tasks within the area of responsibility comply with GMP regulations and related Quality directives. Proactive attitude with a strong results-oriented mindset. Ability to coordinate and train teams. Leadership based on leading by example and collaboration. Flexibility to take on additional responsibilities according to production needs. Strong analytical skills, ability to prioritize, and effective problem-solving. Commitment to quality and continuous improvement. English level B2 for technical and documentation-related communication. Knowledge of SAP for production Main Tasks Organize the production area for sterile and biological products Production planning implementation : Ensure that the relevant production preparations (e.g. personnel arrangement, equipment status, material stock level, environmental quality conditions , Batch Records and the operators, etc.) are all ready to ensure the efficient implementation of the production plan, and dynamic optimize the planning based on the actual sale demand priority and customer’s request. Products delivery : Set appropriate targets, and check and track the production and quality situation daily to ensure that the monthly delivery target can be achieved, and keep a better communication with Planning and Commercial team, quality team to ensure the on-time delivery Production capacity and efficiency improvement: Optimize the production capacity and efficiency to ensure the maximum output, based on good management of the personnel, equipment, material stocks (e.g., raw materials, Intermediate products , Molecular, bulks, diluents, etc.), Manufacturing Batch Records and the related documentations Stock control and management: Establish a good data base of the stocks ((e.g., raw materials, Intermediate Products, Molecular, bulks, diluents, etc.) and ensure the stocks are controlled and managed under a good condition and not affect the rapid progress of production. GMP compliance and improvement of operators performance and skill: Enhance the routine GMP compliance, the continuously training and qualification, to ensure the Right Fist Time Documentation support: Respond quickly and complete quality-related document requirements, as well as documents required by customers. Statistics and analysis of production data: establish a good data base of the production, and based on this, analyze and optimize production management, and improve production and delivery. Conditions Permanent contract, 100% on-site Private health insurance paid for by the company Location: Leganés
JOSE EMILIO P.Active 4 years ago