About this role
Qualification and CSV Technician at Grupo Medinfar. Location: Condeixa-a-Nova, Coimbra District, Portugal. Role: supporting qualification, executing validation, authoring documentation Requirements: Degree in engineering or pharmaceutical sciences (or equivalent experience); 3+ years GMP engineering/operational experience preferred; experience with qualification/validation/CSV, risk-based methods, cGMP/ISO/ICH knowledge, strong communication, English fluency. Category: Engineering Seniority: Mid Level Commitment: Full Time Workplace: Onsite Languages: English