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About the Role This is not a typical IT role, nor is it solely a QA documentation role. We are looking for a person who wants to grow in the area where pharmaceutical manufacturing, computerized systems, GMP compliance, data integrity, and digital transformation meet. The role is suitable for both candidates with initial experience in... • 0–2 years of experience in CSV, IT systems, QA, QC, Production, Engineering, or GMP environment • Fresh graduates are welcome if you are motivated and eager to learn Skills and Mindset • Experience or interest in Power BI, automation, AI, or data analysis • Understanding of GMP, EU GMP Annex 11, CSV, or data integrity principles • Basic knowledge of SQL (nice to...