Junior Pharmaceutical Consultant – Madrid, Spain

Responsibilities

• Resolution of fundamental Computer System Validation compliance issues on assigned projects
• Drafting and reviewing 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 proper deviation report preparation and approval)
• Collaboration in project teams and close interaction with clients, team members and external stakeholders; performing risk assessments

Qualifications

• Bachelor’s Degree in Chemical Engineering (preferred) or related Life Sciences
• Fluent in Spanish and English (at least B2)
• Availabil...