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Posted 18 Jul 2024

MES engineer- Empower

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Employment
Full time
Posted
18 Jul 2024

About the role

MES engineer- Empower

"""we would need these resources to be based out of primarily Bangalore or Pune as an alternative location

""""• Strong Technical Knowledge on Empower & other CDS Systems
• Maintaining and supporting current CDS system
• End user issue support, troubleshooting, & resolution
• Administration of CDS system and server maintenance
• Backup, archival, restore and periodic review of system
• Support in deployment/Installation of CDS applications
• Complete knowledge on user management of lab applications
• Coordinate with multiple instrument vendor during application/instrument setup and instrument qualification
• Hand-holds Site SME’s in Empower operations and implementations through proper training and support
• Experience working in a Pharmaceuticals, Chemical, Manufacturing or any regulated environment....
• Excellent verbal and written communications skills
• Validation of all laboratory and instrument software including maintenance of the Master Validation Plan, functional requirements, risk assessment, and execution of validation protocols
• Data integrity and compliance to 21CFR Part 11 and GxP standards
• Prepare draft and final SOPs and compliance documents


Requirements

MES engineer- Empower

"""we would need these resources to be based out of primarily Bangalore or Pune as an alternative location

""""• Strong Technical Knowledge on Empower & other CDS Systems
• Maintaining and supporting current CDS system
• End user issue support, troubleshooting, & resolution
• Administration of CDS system and server maintenance
• Backup, archival, restore and periodic review of system
• Support in deployment/Installation of CDS applications
• Complete knowledge on user management of lab applications
• Coordinate with multiple instrument vendor during application/instrument setup and instrument qualification
• Hand-holds Site SME’s in Empower operations and implementations through proper training and support
• Experience working in a Pharmaceuticals, Chemical, Manufacturing or any regulated environment....
• Excellent verbal and written communications skills
• Validation of all laboratory and instrument software including maintenance of the Master Validation Plan, functional requirements, risk assessment, and execution of validation protocols
• Data integrity and compliance to 21CFR Part 11 and GxP standards
• Prepare draft and final SOPs and compliance documents


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