Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998, with 40 subsidiaries and more than 2000 employees in Europe, Asia and the Americas. Working in a consulting reality, PQE Group will give you the chance to work on projects for the most important national and international pharmaceutical companies.

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 ens...