JOB PURPOSE:Lead the assigned production lines with 24 hours accountability to deliver business results, planned production volumes in accordance with budget, as well as meeting all the requirements for Safety and Quality, fully applying the Integrated Manufacturing System and respecting Company’s standards and policies. Be the lines owner in terms of people and machine through the Daily Management Systems.KEY RESPONSIBILITIES:• Autonomously lead and set the 24 hours action plan and strategy for the assigned lines during the Daily Direction Setting, to deliver the business results and ensures the follow-up actions are completed. Responsible for oversight of safety, quality, incident elimination and production attainment results.• Drive performance through loss elimination and continuous improvement. Review the 90 days master plans to drive breakthrough results in machine performance, in order to address the losses from unplanned downtime.• Ensure that maintenance task lists for equipment and technological processes are in place and lead the maintenance activities in the assigned production team to ensure stability, predictability and reliability of operations.• Ensure adherence to the standards, full compliance with local legislation, company policies and practices. Adhere to all Quality, Environment and Health, Safety and Security rules, policies and practices.PEOPLE MANAGEMENT AND DEVELOPMENT RESPONSIBILITIES:• Effectively manage and motivate the team to achieve the assigned business results.• Perform regular coaching to develop capabilities of the team on the Daily Management System, according to the Integrated Manufacturing System.• Support the personnel skills and technical development of each team member in order to build ownership and team autonomy.• Build effective working relationships with all stakeholders through good communication, positive attitude and strong collaboration, to enable the team to achieve the business result.

JOB PURPOSE:Lead production activities and processes inside the Manufacturing Area in a consistent, streamlined and strategically aligned way, so that planned volumes are produced according to budgets and are totally compliant with safety and quality requirements. Acting as a role model on the shopfloor, to sustain all the Manufacturing Area processes, supporting the Manufacturing Team and the organization in order to deliver all expected results and objective, with the purpose to foster company business success.KEY RESPONSIBILITIES:• Optimize headcount by creating synergies between productive lines and logistics or other operational departments through effective headcount sharing and allocation.• Contribute to enhance the Process Capability stabilization and knowledge for all needed parameters in order to reach process stability, quality and output maximization.• Ensure GMP roles and accauntabilities are always and strictly followed on the shopfloor.• Deliver the due support in research, define and implement corrective and preventives actions in order to maintain and improve quality standards, gain customer satisfaction and to prevent non-conformities.• Participate as Project Team Member in new projects related such as machines modifications, new machines start-up or new production launches in order to ensure the implementation of the project in a most effective way for the business.PEOPLE MANAGEMENT RESPONSIBILITIES:• Assure that people have the capability, knowledge and skills to execute manufacturing and logistic operations on safety, quality, and time through effective development plan and experiences.• Organize, supervise and coach work of the team members, define their training and development needs based on carreer stages framework.• Ensure efficient relations through all levels of factory by developing effective working relationships with all employee groups, aiming to create positive attitude towards changes and challenges.

JOB PURPOSE:Guarantee operational plans implementation in Sterile Drugs manufacturing, according to the company's objectives in terms of safety normatives, productivity targets and in compliance with Good Manufacturing Practices (GMP), to deliver high quality product and fulfill the needs of the supply chain.KEY RESPONSIBILITIES:• Ensure oversight of processes and activities as well as their compliance with the rules and pharmaceutical procedures, both qualitative and safety.• Early identification of process deviations from the operational plan, ensuring the necessary research into the causes and their solutions.• Active participation in the improvement of process decisions, both technical and organizational.• Ensure proper use of machineries and equipments.• Intensive use of SAP program for management of daily activities, with focus on the production execution and warehouse management modules.• Process notifications for non-compliance qualitative.• Oversee and supervise documentation of batch records, verifying the accuracy of the data and correct compilation so as to work to a consistently high level of GMP compliance.• Revision and drafting of Standard Operating Procedures (SOP) and methods of pharmaceutical industry production.• Make self inspections of machines and production lines to ensure compliance with GMP regulations.• Support successful implementation of new products and processes into the facility, including all appropriate equipment and area changeover activities.• Ensure escalated problems occurring in the area are resolved in a timely manner.PEOPLE MANAGEMENT RESPONSIBILITIES:• Manage, supervise and support the resources according to their abilities and skills.• Contribute to create a climate of respect and mutual confidence for teamwork.• Indipendent managing of shift personnel and related activities.• Demonstrate strong convinction in daily work, taking the initiative to communicate and collaborate with colleagues.

During my Thesis I've performed Metabolomic Analysis of human blood and urine with Nuclear Magnetic Resonance Spectrometer Bruker 400. Working 10 months at the Interdepartmental Great Instruments Centre of University of Modena and Reggio Emilia I learned how to use different softwares such as TopSpin NMR Bruker, XWIN-NMR Bruker and Mnova NMR Masterly Research. Thanks to this experience I have the capabilities needed to independently use these equipment and to interprete the results.