ensuring GMP compliance, integrating PAS-X with enterprise systems, and driving digital transformation within pharmaceutical manufacturing environments. The manager will collaborate with cross-functional teams, oversee system lifecycle activities, and ensure adherence to data integrity and regulatory guidelines.
Lead PAS-X MES implementation, configuration, and support across global/site-level projects.
Define, maintain, and enhance MES architecture aligned with enterprise goals.
Integrate PAS-X MES with ERP systems (SAP), Level 2/3 automation systems, and serialization platforms.
Drive digital transformation and standardization initiatives across manufacturing sites.
Manage system lifecycle activities including upgrades, patches, and performance improvements.
Ensure compliance with GMP, GAMP 5, CFR Part 11, and data integrity principles.
Collaborate with IT, Quality, and Manufacturing teams to harmonize business processes.
Support regulatory audits and validation processes.
Manage vendors and multi-site teams effectively.
Competitive salary and performance bonuses
Health insurance & life insurance
Opportunities for global project exposure
Professional development and certification support
Work-from-home flexibility depending on project
Onsite travel opportunities
Paid leaves and annual bonus
Employee wellness programs
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