Senior Pharmaceutical Validation Specialist

beBeeProcessValidation; Madrid; Presencial; EUR 50.000 - 70.000; Jornada completa

Descripción de la vacante

A pharmaceutical company in Madrid is seeking a Process Validation Expert to ensure that products meet the highest quality standards. The ideal candidate must have over 5 years of experience in pharmaceutical validation, preferably with sterile products, and a strong understanding of GMP requirements. This is a great opportunity to develop and execute validation master plans in a collaborative environment.

Formación

• 5+ years of experience in pharmaceutical validation, ideally with sterile products.
• Strong understanding of GMP requirements.
• Experience with quality management systems.

Responsabilidades

• Develop and execute validation master plans.
• Prepare validation protocols and documentation.
• Collaborate with production and quality teams.

Conocimientos

Quality Assurance

Process Validation

Technical Writing

Educación

Degree in Pharmacy or Life Sciences

Herramientas

TrackWise

SAP

Descripción del empleo

Overview

Process Validation Expert – We are seeking a highly motivated and experienced Process Validation Expert to join our team. As a key quality professional, you will be responsible for developing and executing validation protocols in compliance with Good Manufacturing Practices (GMP) standards.

The ideal candidate will have a strong background in Quality Assurance, preferably in the pharmaceutical industry. Your experience in process validation will enable us to ensure that our products meet the highest quality standards.

Key Responsibilities

• Develop and execute validation master plans for process and cleaning validation
• Prepare validation protocols, reports, and supporting documentation
• Ensure validation activities meet GMP requirements and internal quality policies
• Collaborate with production, quality control, and engineering teams to implement validation strategies
• Perform risk assessments and contribute to corrective action prevention programs
• Support site audits and inspections
• Contribute to quality system improvements and revalidation of ISO certifications

Requirements

• Degree in Pharmacy or Life Sciences
• 5+ years of experience in pharmaceutical validation, ideally with sterile products
• Strong understanding of GMP requirements
• Experience with systems like TrackWise, SAP, or similar QMS tools
• High level of English proficiency
• Excellent attention to detail, technical writing skills, and ability to work collaboratively