Production Supervisor

for the site Borgo San Michele LT, Italy Would you like to make a valuable contribution to the health of patients? And do something really meaningful on your own responsibility? Then we look forward to hearing from you! Excellence beyond manufacturing - that's what we stand for as Aenova, one of the world's leading contract manufacturers and developers for the pharmaceutical industry with 4,000 employees at 15 sites. Latina is a leading centre of excellence in sterile liquid production, with a strategic investment plan to become one of Europe's foremost hubs. Production Supervisor for the site Borgo San Michele LT, Italy Would you like to make a valuable contribution to the health of patients? And do something really meaningful on your own responsibility? Then we look forward to hearing from you! Excellence beyond manufacturing - that's what we stand for as Aenova, one of the world's leading contract manufacturers and developers for the pharmaceutical industry with 4,000 employees at 15 sites. Latina is a leading centre of excellence in sterile liquid production, with a strategic investment plan to become one of Europe's foremost hubs. Your key responsibilities To grant the correct execution of the department Tiers. To verify the feasibility of mid-term production plans with respect to available resources and market priorities. Also, to share any differences with the manager of the unit. Coordination with the Technical Assistance Unit, in order to grant the correct action time on the machines and reduce downtime. To support the section manager and the colleagues involved, in reviewing operational procedures,“DVR” and budget plans. To suggest innovative solutions to improve productive processes and reduce costs. Constantly and regularly, to communicate with the operational personnel with the aim to transfer information and respond to necessities or suggestions of improvement. To ensure that personnel respects EHS and GMP regulations. To participate actively as SME to regulatory and customer inspections. To assure the opening of deviations in case of anomalies compared to flows and processes. To promote/participate to the definition of change plan and CAPA plan for the own area of competence. Participate proactively to projects that impact on the own area of competence taking part on team projects. Ensure that the documentation for Batch Record (supporting validation protocols) is implemented correctly and delivered within the set time frame. To define training plan for employees and guarantee that the personnel is trained on procedures and that have the technical education of the various work centre to which it is assigned. To ensure the definition of standard of machine and labour hour for the products of own areas of competence according with the section manager. Your profile University degree in technical subjects preferred (Engineering, Chemistry, Pharmaceutical Chemistry, etc.,). 3-5 years of People management experience. Good knowledge of GMP. Good knowledge of Oral Solid Dosage form. Good knowledge of English both written and spoken. Excellent knowledge of Office. Good knowledge of SAP system. Lean Six Sigma certification is a plus. Strong analytical approach with a high level of accuracy and attention to detail. Strong problem-solving and organizational skills. Ability to manage multiple priorities and work effectively under tight deadlines. Proactive mindset with a continuous improvement approach. Your motivation Are you looking for new challenges in a highly competitive environment? And you want to tackle them creativelyand on your own responsibility? Do you prefer a "get-it-done" culture and think in terms of solutions ratherthan problems? What are you waiting for? We would be happy to explain our corporate benefits in a personalconversation! #J-18808-Ljbffr