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

Project Delivery Partners Pte Ltd; Madrid; On-site; Full time

Benefits offered by this job

Competitive salary

Professional development opportunities

Dynamic work environment

Job summary

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.

Qualifications

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

Responsibilities

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

Skills

Fluent in Spanish

Fluent in English

Project management skills

Analytical skills

Excellent communication skills

Education

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

Tools

GMP guidelines

Validation protocols

Change Management processes

Job description

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.