Vincenzo Cerciello
Pharma operations manager at Doppel Farmaceutici- Claim this Profile
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Italiano Native or bilingual proficiency
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Inglese Professional working proficiency
Topline Score
Bio
Credentials
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Green Belt certified Lean Six Sigma(LSS-GB)
Accademia del Lean Six SigmaMar, 2017- Nov, 2024
Experience
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Doppel Farmaceutici
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Italy
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Pharmaceutical Manufacturing
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200 - 300 Employee
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Pharma operations manager
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Jun 2021 - Present
- Responsible of Production- Responsible of Maintenance - Plans and realizes, through the coordination of the assigned resources, production (Packaging and Manufacturing) on time and in the foreseen quantity- Guarantees compliance with the quality standards defined and compliance with GMPs through constant checks during the manufacturing process, identifies the causes of deviations and activates appropriate corrective actions- Contributes to the drafting, revision and updating of the procedures of the departments under his responsibility by signing them for approval- Lead inspections during ministerial and customer audit- Responsible for people under his responsibility, including people development (e.g. trainings, performance, etc.)- Responsible of Maintenance plan for the production equipment - Assure individual project deliverables are achieved, cultivates and manages relationships with preference partners.- Develops and manages to an annual budget designed to meet or exceed objectives by continuous review of performance against project KPIs. Show less
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Manufacturing Manager
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Oct 2018 - Present
- Performs its functions in the employ of Site Head and takes care of the production of solid, semi-solid and liquid materials- Organizes supervises and coordinates the activity of the relevant sector on the basis of Good Manufacturing Practices- Plans and realizes, through the coordination of the resources assigned, the production in the time and in the foreseen quantity- Participates in production planning as far as the sector of its competence is concerned- Ensures compliance with the defined quality standards and compliance with GMPs through constant controls during the manufacturing process, identifies the causes of the deviations and activates appropriate corrective actions- Instructs and trains staff both in the initial training phase and following technology changes and helps to improve the performance of each one in order to achieve a good quality of production- Contributes to the drafting and updating of the manufacturing masters- Contributes to the drafting of the revision and updating of the procedures of the departments of its competence, signing them for approval- checks the correct recording of the data required by the individual manufacturing documents, batch records and signs them for approval.- Verifies the efficiency of its departments, premises and equipment and ensures their maintenance and validation- Ensures that all activities are carried out in compliance with current safety regulations- Trains and supervises the correct environmental behavior in compliance with the Management System adopted by the Company. Show less
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Delpharm
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France
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Pharmaceutical Manufacturing
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700 & Above Employee
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Shift Supervisor
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Sep 2017 - Sep 2018
- Managing people in accordance with the internal rules on the presence of the job, taking appropriate time feedback and / or climbing any critical situations that require disciplinary action; - Administrative management of production personnel (holidays, permits, illnesses, performance managment) - Ensure compliance with safety, health and environment norms - Manage production flow in line with departmental priorities and requirements (eg allocations, approaches, field documentation management, consumer good etc) - Ensure alignment within the group to a common way of managing information, interacting with people, and achieving results - Participate actively in the management of deviations both through proper detection and reporting of the same as part of the investigation team (root cause analysis, evaluation of appropriate preventive or corrective actions) - KPI management (OEE of production lines, Tier KPIs, Quality KPIs) - Manage production flow in line with departmental priorities and requirements (eg allocations, approaches, field documentation management, consumer good etc) - Manage the needs of the department including critical communication to the manager Autonomy in house keeping management interfacing with support departments by running quality Gemba Walk and Fit for Use; - Adopt an appropriate escalation process (CP compilation and follow up or quality critical assessment - flows, processes, procedures, with area manager) - Driving staff at the time of site transition, assessing behaviors, and sharing information Show less
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Roche
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Switzerland
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Biotechnology Research
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700 & Above Employee
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Shift Supervisor
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Apr 2017 - Aug 2017
- Managing people in accordance with the internal rules on the presence of the job, taking appropriate time feedback and / or climbing any critical situations that require disciplinary action; - Administrative management of production personnel (holidays, permits, illnesses, performance managment)- Ensure compliance with safety, health and environment norms- Manage production flow in line with departmental priorities and requirements (eg allocations, approaches, field documentation management, consumer good etc) - Ensure alignment within the group to a common way of managing information, interacting with people, and achieving results- Participate actively in the management of deviations both through proper detection and reporting of the same as part of the investigation team (root cause analysis, evaluation of appropriate preventive or corrective actions)- KPI management (OEE of production lines, Tier KPIs, Quality KPIs)- Manage production flow in line with departmental priorities and requirements (eg allocations, approaches, field documentation management, consumer good etc) - Manage the needs of the department including critical communication to the manager Autonomy in house keeping management interfacing with support departments by running quality Gemba Walk and Fit for Use; - Adopt an appropriate escalation process (CP compilation and follow up or quality critical assessment - flows, processes, procedures, with area manager) - Driving staff at the time of site transition, assessing behaviors, and sharing information Show less
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Solid Manufacturing Continous improvement coordinator
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Feb 2016 - Apr 2017
- Definition, implementation and monitoring of KPIs that can provide a structured and reliable view of the productivity and efficiency of the department: leading and lagging KPIs, tiered accountability, capacity management, dashboard design and OEE management.- Identify bottleneck and Implement actions to improve the efficiency of the Solid Manufacturing department - Analyze processes and workflows in order to eliminate waste and non-value added processes of the department using methodologies such as DMAIC, SIPOC, SMED / changeover optimization, 5S, value stream mapping, time value map, etc.- Implementation of LSS methodology (Lean Six Sigma) that combines the techniques belonging to the Six Sigma (statistical methods for control and process improvement) to those of lean manufacturing or lean production- Creating effective working documents (SOPs, Cards, SRD ...) and running training for these documents- Collaborate with all the function in the Solid Manufacturing Department and facilitate the implementation of improvement Action- Monitor the results achieved, providing internal information to the management of the site in case of a significant change of trend. Show less
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Packaging Continous Improvement Coordinator
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Oct 2014 - Feb 2016
- Actively contribute to the Continuous Improvements activity- Collect and analyze data on the OEE and productivity of the Packing department- Identify bottleneck and Implement actions to improve the efficiency of the packaging department - Responsible of the implementation of Continuous Improvement tools and methodology (Dashboard, Kanban, 5s, SMED, Stream Value Map)- Collaborate with all the function in the Packaging Department and facilitate the implementation of improvement Action Show less
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Packaging Intern
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Jul 2014 - Oct 2014
- Responsible of the new high containment packaging line, from a general to a technical knowledge that brought me being the responsible of Performance Qualification and trainer for packaging operators;- Preparing SOPs, Master Batch Records and relative documents regarding packaging lines and department;- Support in packaging department projects with Project Management Office, Engineering and Maintenance, Quality Assurance, Quality Validation and Risk Assessment groups;
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Kraft Heinz
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United States
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Food and Beverage Services
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700 & Above Employee
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Internship
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Jan 2014 - Mar 2014
- Led studies on the dissolved oxygen in different food matrix at the aseptic plant in Latina site. - Worked in team to develop, from the obtained results, a possible solution to improve the process of the plant and reduce the scrap of the production. - Took part to an intensive course on the continuous improvement (Yellow belt) - Led studies on the dissolved oxygen in different food matrix at the aseptic plant in Latina site. - Worked in team to develop, from the obtained results, a possible solution to improve the process of the plant and reduce the scrap of the production. - Took part to an intensive course on the continuous improvement (Yellow belt)
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Aarhus University
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Denmark
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Research
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700 & Above Employee
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Master thesis internship
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Feb 2012 - Oct 2012
During this experience abroad I have worked on the isolation of a novel aerotolerant denitrifier Bacillus abundant in soil. I improved my teamwork attitude in a stimulant multicultural environment. I have also developed a problem solving approach working alone on the isolation and characterization of a novel Bacillus. One of my specific task was to investigate the tolerance of the strain towards oxygen as well as the ability of the strain to grow on nitrate. In order to study the properties I used micro-electrodes to follow the oxygen consumption behavior as well as the release of-nitrogen dioxide by the strain. In addition, I also investigated the denitrification capacity of the strain and its tolerance towards nitrite, which is a strong cyto-toxin. In order to perform all those studies I also collaborated to implement a bioreactor (laboratory scale) that would allowed to follow the metabolism of the strain during the growth. Show less
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University of Naples Federico II
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Higher Education
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700 & Above Employee
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apprentice
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Sep 2009 - Jan 2010
Internship and work thesis. Optimization of a medium for the production of recombinant protein. Internship and work thesis. Optimization of a medium for the production of recombinant protein.
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Education
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2013 - 2014
Università degli Studi di Napoli 'Federico II'
second level professional master's programmes, Ottimizzazione ed innovazione di processo nelle produzioni alimentari -
2011 - 2013
Università degli Studi di Napoli 'Federico II'
Master's degree, Biotechnology -
2012 - 2012
Aarhus Universitet / Aarhus University
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2006 - 2010
Università degli Studi di Napoli 'Federico II'
Bachelor's degree, Biotechnology
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