3 - 8 years
5 - 10 Lacs
Posted:1 week ago|
Platform:
Work from Office
Full Time
We are looking for an experienced MES Engineer with strong knowledge in Siemens Opcenter Execution Pharma to support the implementation and lifecycle management of MES solutions within GMP-compliant pharmaceutical manufacturing environments. This role involves configuring electronic batch records integrating with other systems (ERP SCADA LIMS) and ensuring regulatory compliance. Key Responsibilities: Configure test and deploy MES solutions using Siemens Opcenter Execution Pharma. Design and implement Electronic Batch Records (EBRs) based on process requirements. Work closely with manufacturing QA and automation teams to gather and translate business requirements. Ensure system validation and documentation according to GMP and GAMP 5 guidelines. Support system integration with ERP LIMS and automation layers (ISA-95 model). Troubleshoot MES application issues and provide operational support. Maintain SOPs technical specifications and validation documentation. Contribute to audits inspections and data integrity compliance. Skills & Attributes: Strong experience with Siemens Opcenter Execution Pharma (formerly SIMATIC IT eBR). Deep understanding of pharmaceutical processes and regulatory frameworks (21 CFR Part 11 GAMP). Proficient in creating and validating EBRs recipe modeling and MES workflows. Knowledge of system integration especially with SAP SCADA/DCS and LIMS. Excellent analytical documentation and communication skills. Team-oriented with a proactive approach to problem-solving. Ability to work in cross-functional and regulated environments. Contact Person : - Anusiya Contact Number : - 9840114871 Location : - Pan India
Golden Opportunities Pvt Ltd
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