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Overview
Elevate your career with LAPORTE as a Senior Pharmaceutical Validation Engineer based in Greater Calgary. Utilize your expertise in GMP compliance and validation to support clients and enhance quality standards in the pharmaceutical industry. Responsibilities
Draft master validation documents like Validation Master Plans Execute qualification protocols (IQ/OQ/PQ) for systems Ensure GMP compliance during validation activities Support QA teams in managing change notices Manage client accounts and maintain relationships Requirements
Bachelor’s or master’s degree in science or engineering 5+ years in the pharmaceutical manufacturing or consulting Robust knowledge of GMP standards Familiar with pharmaceutical manufacturing processes Willingness to travel to client sites
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Elevate your career with LAPORTE as a Senior Pharmaceutical Validation Engineer based in Greater Calgary. Utilize your expertise in GMP compliance and validation to support clients and enhance quality standards in the pharmaceutical industry. Responsibilities
Draft master validation documents like Validation Master Plans Execute qualification protocols (IQ/OQ/PQ) for systems Ensure GMP compliance during validation activities Support QA teams in managing change notices Manage client accounts and maintain relationships Requirements
Bachelor’s or master’s degree in science or engineering 5+ years in the pharmaceutical manufacturing or consulting Robust knowledge of GMP standards Familiar with pharmaceutical manufacturing processes Willingness to travel to client sites
#J-18808-Ljbffr
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