PQE Group seeks a CQV Consultant in Barcelona to lead qualification and validation activities for biotechnological production facilities. You will work on C&Q; activities and associated documentation, ensuring compliance with GMP, FDA, EMA, and ICH standards across cross-functional teams.
Adecuado candidates hold a life sciences or engineering degree, with 2+ years in IQ/OQ/PQ protocol development and strong English/Spanish communication skills.
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📌 Barcelona CQV Consultant: Pharma & Biotech Validation (Cataluña)
🏢 Pqe Group
📍 Cataluña
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