Consultor Pharma (Marzán)

Full-time Bio-farmacéutico y salud

Responsibilities

• Resolution of fundamental Computer System Validation compliance issues on assigned projects
• Drafting and review of main validation deliverables such as Validation Plan , User Requirement Specification , Functional Design Specification , Risk Analysis, Test Plans (FAT, SAT, DQ, IQ, OQ, PQ), Test & Validation Reports
• Planning and coordinating measures to maintain GMP compliance
• Ensure all project-related issues and deviations are recorded, approved and dispensed accordingly (including ensuring proper deviation report preparation and approval)
• Collaboration in project teams and close interaction with clients , team members and external stakeholders
• Performing of risk assessments

Qualifications

• Bachelor’s Degree in Chemical engineering (preferred) or related to Life Science sector
• Fluent in Spanish and English (at least B2)
• Availability to travel

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