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Niche MES/GxP skills and Level-2 automation reduce applicant density despite Bangalore location.
High—MES and GxP expertise is industry-specific and not easily transferable across sectors.
Mandatory MES/PAS-X, GxP and Level-2 automation experience enforces strict candidate filters.
Design and parameterize Master Batch Records (MBRs) and Electronic Signature Protocols (ESPs) for manufacturing execution systems in a regulated GxP environment.
Develop process value libraries and graphical recipe structures for generic and product-specific batch records to optimize production efficiency.
Map and manage integration points between MES and Level 2 automation systems (SCADA, PLC, DCS) including material flow and equipment tracking logic, and deliver regulatory documentation including specifications and qualification scripts.
5-12 years of experience in MES design and implementation.
Experience with MBR/ESP design in regulated GxP environments mandatory.
Proficiency in integration between MES and Level 2 automation systems (e.g., SCADA, PLC, DCS).
Work Experience Required: 5-12 years. Notice Period: Not explicitly mentioned in the JD.
Experienced in designing and documenting MES solutions with deep understanding of batch record structures and automation integration.
Comfortable operating within regulated pharmaceutical or similar GxP-compliant manufacturing environments.
Ability to translate paper-based pharmaceutical processes into digital MES formats and produce detailed technical and testing documentation.