V.I.E Qualification & Validation engineer (M/F)
Core
Coordinate and execute validation cycles for pharmaceutical and health-related product production projects, ensuring compliance with GMP standards and project timelines.
Role type
Validation Engineer (Pharmaceutical Manufacturing)
Builds
Validated production equipment and manufacturing processes for pharmaceutical partners
Domain
Pharmaceutical industry / GMP compliance
Deliverable
client delivery
Required skills
GMP environment experience, risk assessment, functional and design specification drafting, test protocol execution (URS/FAT/SAT/IQ/OQ/PQ), deviation management, CAPA implementation, training delivery
Preferred skills
Knowledge of production processes, equipment familiarity
Technologies
Validation software suites, GMP documentation systems
Responsibilities
Represent the Validation department on projects, design validation strategies, coordinate project planning with stakeholders, draft risk assessments and specifications, execute and analyze test results, manage deviations and CAPAs, develop training sessions
Seniority
Mid-level, hands-on IC
