QA Validations Lead – GMP, Madrid (On-Site Weekends)

Project Delivery Partners Pte Ltd; Madrid; Presencial; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Competitive salary

Professional development opportunities

Dynamic work environment

Descripción de la vacante

A leading pharmaceutical consulting firm in Madrid is seeking a QA Validations Expert to oversee validation activities within the manufacturing and laboratory environments, ensuring compliance with industry standards. The ideal candidate will have substantial experience in pharmaceutical QA and validation, including knowledge of GMP and regulatory guidelines. This full-time position requires fluency in both Spanish and English, offering opportunities for professional development in a dynamic workspace.

Formación

• Minimum 5 years of experience in pharmaceutical QA qualifications and validation.
• Strong knowledge of GMP, GDP, and regulatory guidelines.
• Experience with sterile dosage forms.

Responsabilidades

• Lead validation activities across manufacturing, laboratory, and computerized systems.
• Ensure compliance with FDA, EMA, ICH regulations.
• Manage deviations and propose corrective actions.

Conocimientos

Fluent in Spanish

Fluent in English

Project management skills

Analytical skills

Excellent communication skills

Educación

Bachelor's or Master's degree in Pharmacy, Chemistry, Biotechnology, Engineering

Herramientas

GMP guidelines

Validation protocols

Change Management processes

Descripción del empleo

A leading pharmaceutical consulting firm in Madrid is seeking a QA Validations Expert to oversee validation activities within the manufacturing and laboratory environments, ensuring compliance with industry standards. The ideal candidate will have substantial experience in pharmaceutical QA and validation, including knowledge of GMP and regulatory guidelines. This full-time position requires fluency in both Spanish and English, offering opportunities for professional development in a dynamic workspace.