Experience

Almirall

• Spain
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Director Técnico Farmacéutico en Industrias Famacéuticas Almirall S.A. - Qualified Person

  • Jan 2011 - Present

  The Qualified Person of manufacturing laboratory assumes the responsibilities described for this function under Article 54 of Directive 2001/183 / EC, transposed into Spanish law 29/2006 and developed in the RD 824/2010, as well as other internal responsibilities for the role.

• Site Responsible en Industrias Farmacéuticas Almirall S.A.

  • Jan 2014 - Present

  Ensure compliance with good manufacturing practice as well as specific health regulations, through the implementation of quality system and established work procedures for activities related to the production of their responsibility center.

• Quality Assurance Operations Manager

  • Jan 2014 - Present

  Ensure pharmaceutical quality systems or production plants meet cGMP's Almirall Comply with corporate policies in order to ensure the safety, efficacy and quality of pharmaceuticals products

• Quality Assurance Unit Operations

  • Jan 2011 - Dec 2015

• Quality Assurance Unit Validations - Qualifications

  • Jan 2011 - Dec 2011

• Qualified Person - Director Técnico

  • Jan 2010 - Dec 2011

• Quality Assurance Unit Operations

  • Jun 2002 - Jan 2011

• Technical Responsible for Production

  • Jan 2002 - Dec 2002



LDP Laboratorios Torlan S.A.

• Spain
• Pharmaceutical Manufacturing
• 1 - 100 Employee

• Pharma Operations Direction

  • Jan 1998 - Jan 2002

• Production Unit Manager

  • Oct 1995 - Jan 1998



Parc Tauli Hospital Consortium

• Cerdanyola del Vallès (Barcelona)

• Pharmaceutical Pharmacy Service

  • Oct 1992 - Oct 1994