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Mid-level generalist title, metro location, and popular role amplify applicant competition.
MES and pharmaceutical regulatory experience are domain-specific and less transferable across industries.
Explicit years, mandatory MES Opcenter experience, and regulatory compliance skills increase filter strictness.
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Owns delivery and 2nd level support of AspenTech MES applications including issue resolution, incident management, and change management.
Leads and coordinates MES implementation and upgrade projects from requirement gathering through qualification to final delivery.
Ensures integration of MES with Level 2, 3, and 4 systems such as SAP ERP, OSI PI, and LIMS; responsible for executing maintenance activities and system improvements.
Bachelor’s degree in Science or Engineering related to IT, Computer Science, Electronics, Instrumentation, or Pharmacy.
Minimum 5-6 years experience with AspenTech MES applications (versions V11, V12, V14.5) with at least 3 years hands-on experience with MES Opcenter Ex MDD module.
Experience in pharmaceutical or life sciences manufacturing processes and MES integration with multiple systems (SAP ERP, OSI PI, LIMS).
Experience with Incident Management, Problem Management, Change and Release Management; ability to work shifts and independently.
Experienced MES application expert with deep knowledge of AspenTech MES suite and Opcenter MES, including configuration, integration, analytics, and reporting.
Practical understanding of pharmaceutical manufacturing processes and regulatory compliance standards (21CFR Part 11, cGMP, GAMP, EU Annex 11).
Able to lead end-to-end MES delivery projects, technically proficient in MES platform support, and comfortable working in global service delivery model with minimal supervision.