Head Of Quality

• Apr 2022 - Present

Quality and Manufacturing Global Cross functional Director

• Jan 2020 - Dec 2021

As consolidate expert on Pharmaceutical Manufacturing and Quality my function was to define and design the processes to harmonize among the Sanofi Industrial work and define how the systems ( Oracle or SAP ) are configuration to deploy the processes.

Quality Manager and QP pharmaceutical Spain

• Apr 2004 - Dec 2019

Main Achievements:- Quality program deployment during last 5 years with an achievement of 90 % in average.- Established Quality Committee since 2006.- Local deployment of Quality risk Management- Coordination of Quality teams (Regulatory Site Officer, QAP, QAS,QC and Analytical development ) to improve the quality level in the whole activities of the site.- Development of program to create back up of key positions and main activities within quality.- Creation of auditor team of 10 persons.- Management of audits and authorities inspections. Strong experience in international registration with documentary application and inspection based. Excellent relationship with Catalan and Spanish central authorities, Servei Catala de la Salut and AEMPS. Since 2009 inspections from AEMPS for MAJOR changes in premises.-Deployed performance programs in Quality, reduction of QC lead time from 11 days to 4,5 days, and release time from 5 days to 2,5 days.- Development of transfer projects: regulatory, manufacturing, analytical.- Established program of standardization and simplification of methods and quality processes to increase performance.- Management of deployment of corporate applications for: supplier management, Change Control, Deviation CAPA, Documentation, complaints, suppliers audits, Risk management, Sample Manager, ERP….- Participation in European Innovation award with European Commission of research and innovation (H2020), obtained honor mention for the submitted innovative project.- Participation in international quality commissions.- Deployment of innovative systems for training and working instructions.- Coordination of serialization & aggregation project inside the plant.- Strong experience on materials suppliers management, established a local organization to reduce mono sourcing of materials.- Management of team: 64 persons including routine and projects. Show less

Quality Manager pharmaceutical France

• Feb 2017 - Jul 2017

Short term assignment . In addition to my position in Spain I was required to move temporary to France to help one site in development of quality systems and enhancement:To maintain the activity during the period on which the new quality manager will join the site.To contribute in the readiness for ANSM inspection, unannounced for Sep-17.To contribute to the performance within the Quality organization/activity.To lead actions, plan to fix or recover some delays. To participate in the integration of the new Quality Manager Show less

Manufacturing Director in Pharmaceutical Site

• Apr 1999 - Mar 2004

Contribution to transfer more than 40 products from outside of Sanofi and others S-Aplants.- Commissioning and startup of 4 new packaging lines.- Productivity program 2000-2003 to increase: yield (+15 k€/year ), TRS ( 30 % ) and reduction of staff.- Program to issue all lines, products and processes documents.- Program to develop back up of technicians and responsible.- Reduction of complaint (less 1ppm)- Reduction of non-productivity and non-quality activities.- Deployment of an organization with specialist by activity- Management of a team: 90 persons Show less

Industrial pharmaceutical development Manager

• Dec 1997 - Mar 1999

Established a system of assessment for product with an action plan to improve the qualityand productivity.Defined equipment of small size to scale up most of products and technologies available.Commissioning and startup of fluid bed equipment and validation of key products.- Commissioning and startup of coating pan big size and validation of key products.

Manufacturing Responsible

• Apr 1992 - Nov 1997

- New facilities design and startup (1992-1994)- Training of staff for new technologies and premises.- To organize the team from 1 shift to 3 due to the increase of activity due to transfers - Transfer responsible dry products to Riells.- Defined system to create and maintain products, equipment and processes documentation.

Pharmaceutical Development Technician

• Mar 1990 - Mar 1992

Industrialization o 2 key products for the company. Galenic development of 2 ethical products, one of them with an award to the development granted by Spanish MoH AEMPS. Program of development in different products to improve taste and flavor. Development and industrialization of dietetic products, n.1 in Spain (BIOMANAN®) Industrialization o 2 key products for the company. Galenic development of 2 ethical products, one of them with an award to the development granted by Spanish MoH AEMPS. Program of development in different products to improve taste and flavor. Development and industrialization of dietetic products, n.1 in Spain (BIOMANAN®)

Laboratory Technician

• Oct 1987 - Mar 1990

My first long term contract in a laboratory of diagnosis as technician, preparing samples, processing samples for the evaluation of the Doctors.This job was combined with my studies in Barcelona University to obtain my Pharmacist Degree, granted in 1990.

Hospitalary pharmacy trainee

• Jul 1984 - Sep 1987

Collaboration in the hospital to develop my skill in job performance, first experiences to have responsibilities, work in a team, to understand how one Department is organized and to learn how one leader/boss manage the team and activity.