Applied Pharmaceutical Innovation (API) seeks a hands-on CSV validation qualified to lead the validation lifecycle for software systems in GMP environments at our Edmonton-based operations. You will collaborate with Quality, Engineering and IT to develop IQ/OQ/PQ protocols, manage change control, and ensure compliance with Health Canada and FDA guidelines, including 21 CFR11 and GAMP5. This on-site role requires 3–5 years of experience, a Canadian degree, and a proactive, results-driven
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📌 GMP IT CSV Specialist: ERP & Electronic Systems Validation (Winnipeg)
🏢 Run my Accounts
📍 Winnipeg
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