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Senior Pharmaceutical Mes Systems Consultant

Amaris Consulting

Support GMP-regulated pharmaceutical and biotechnology manufacturing through MES configuration, validation, and electronic batch record expertise.This senior consulting position focuses on manufacturing execution systems in regulated pharmaceutical or biotechnology environments. You will configure and support MES solutions, electronic batch records, recipes, workflows, and enterprise integrations. The role also includes testing, deployment, commissioning, qualification, and go-live support.Key Responsibilities:
Configure electronic batch records and master batch recordsSupport recipes, workflows, testing, and MES deploymentIntegrate equipment and enterprise systems through interfacesSupport commissioning, qualification, go-live, and hypercareMentor junior consultants and share client knowledgeRequirements:
Five years in manufacturing systems, MES, or industrial dataThree listed technologies required, with fourth working knowledgeSiemens MES, Ignition, Aspen, or SAP PCo experienceGMP, CSV, data integrity, OPC, and SQL knowledgeFluent English and Canadian Eastern Time availabilityBring senior MES delivery, electronic batch record, validation, and regulated manufacturing experience to pharmaceutical systems projects.
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Vacancy posted 53 minutes ago
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