SRS Consulting Inc
Job Description:
A dynamic professional with proven expertise in
Siemens Opcenter Medical Devices in Manufacturing Execution domain. Design and architect multi-site MES Opcenter implementation based on discussion with business teams and their processes Should have Experience on
LOFTWARE PRISYM 360 Understand the paper Batch record and business process flow in collaboration with business SMEs Expertise in high-performance, cross-functional teams developing, and supporting information systems in the Medical Device and pharmaceutical manufacturing industries Data-driven, user-centric, technology, and information solutions business systems analyst with a deep understanding of business processes under GxP, ISO, and regulatory compliance Knowledge of Mfg. Process Controls and Reporting program Awareness of Electronic Lot History Records
using Camstar/OpCenter Software for Medical Device/ Pharma industries Implement and execute the shopfloor transaction using OpCenter Execution Discrete in Discrete manufacturing Industry Experienced in Camstar (V8.x) Modeling Configuration, Designer, OpCenter Connect MOM, OpCenter Connect cloud, Portal studio Design and architect the interfaces and middleware data transfers with the OpCenter solution Author Computer System Validation (CSV) documents such as Functional Risk Assessment, Validation Plan, System Test Plan, Test Summary Reports (IQ/OQ/UAT), Validation Report, etc. following industry standard GAMS 5 and/or following the client Quality standards. Author and review test scripts (IQ, OQ, PQ) Perform IQ (application and devices), OQ (including the Siemens CAMSTAR / OpCenter MES System integration with SAP, PAC and other L3/L2 systems) Assist Recipe Author / Modeler in Key user and end user training content creation based on the standard Siemens CAMSTAR / OpCenter MES System product training material Assist CoE and Site in conducting End user training
Siemens Opcenter Medical Devices in Manufacturing Execution domain. Design and architect multi-site MES Opcenter implementation based on discussion with business teams and their processes Should have Experience on
LOFTWARE PRISYM 360 Understand the paper Batch record and business process flow in collaboration with business SMEs Expertise in high-performance, cross-functional teams developing, and supporting information systems in the Medical Device and pharmaceutical manufacturing industries Data-driven, user-centric, technology, and information solutions business systems analyst with a deep understanding of business processes under GxP, ISO, and regulatory compliance Knowledge of Mfg. Process Controls and Reporting program Awareness of Electronic Lot History Records
using Camstar/OpCenter Software for Medical Device/ Pharma industries Implement and execute the shopfloor transaction using OpCenter Execution Discrete in Discrete manufacturing Industry Experienced in Camstar (V8.x) Modeling Configuration, Designer, OpCenter Connect MOM, OpCenter Connect cloud, Portal studio Design and architect the interfaces and middleware data transfers with the OpCenter solution Author Computer System Validation (CSV) documents such as Functional Risk Assessment, Validation Plan, System Test Plan, Test Summary Reports (IQ/OQ/UAT), Validation Report, etc. following industry standard GAMS 5 and/or following the client Quality standards. Author and review test scripts (IQ, OQ, PQ) Perform IQ (application and devices), OQ (including the Siemens CAMSTAR / OpCenter MES System integration with SAP, PAC and other L3/L2 systems) Assist Recipe Author / Modeler in Key user and end user training content creation based on the standard Siemens CAMSTAR / OpCenter MES System product training material Assist CoE and Site in conducting End user training