INSUD PHARMA, operating across the pharmaceutical value chain, seeks a QA EBR Technician in León to review and approve Electronic Batch Records, ensuring data integrity and GMP compliance in batch documentation.
You will develop SOPs for EBR management, support deviations and change controls, and collaborate with Production, Engineering and QA teams. English-Bilingual and 1–3 years in GMP documentation required.
📌 QA EBR Specialist: GMP Documentation & Compliance (Castilla y León)
🏢 Chemo
📍 Castilla y León
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