*Role1: Camstar MES Consultant* *Location: *Portage, MI
*Duration: *6+ Months *Key Requirements* · Experience in development of Camstar MES UI and tools · Oracle MFG SOA Integrations · .NET software development experience · ASP.NET (VB) Web application development experience · Experience of ASP.NET / C# / AJAX / C++ / VB and C# using .Net · Experience with XML technologies (XML, XSD and XSLT ) · Experience with HTML, DHTML, and XHTML. · Experience of .NET Frameworks · Experience working with SQL and/or Oracle *Role2: Senior MES Business Analyst* *Location: *Portage, MI *Duration: *6+ Months *Description:* · Experience as a business analyst; prefer experience in a technical/business discipline · Demonstrated understanding of general manufacturing business processes · Prefer experience in the Medical Device industry · Demonstrated ability to manage project tasks, including coordination of specific tasks/activities of a technical project · Demonstrated understanding of Camstar Manufacturing Execution Systems (MES) concepts around a single with an international, multi-org setting · Experience with OPC Servers · Experience with PLC *Role3: MES Validation Lead* *Location: CA* *Duration: 5+ Months* *Description* Candidate should be having 2-3 MES implementation experience in medical device industry and will perform following tasks: · Develop and Execute MES Full eDHR release validation plan document, IQ, OQ & PQ Protocols · Develop MES release Task and Validation plan report · IQ, OQ, PQ Protocol Execution support and Task Report Development and Approval Support · Closing Validation Plan Report development and Approval Support · MES Project related Procedures Development / Update & Approval Support *Role4: MES Business Analyst* *Location: CA* *Duration: 6+ Months* *Description:* · Development of Business and Line requirements to implement MES for Full eDHR · Development of Manufacturing and Quality IPC Process Flows for production lines · Development of Training Materials for MES next release *Role5: MES Lead Consultant* *Location: CA* *Duration: 6+ Months* *Description:* · Hands-on Project Management support for Re-engineering phase, full eDHR release for medical device lines. · Coordinate and assist on execution of IQ, OQ and PQ protocol for MES release and Full eDHR release · Assist on the development of Business and Line requirements for MES release and Full eDHR release · Assess the differences between the different lines of manufacturing process to coordinate the modification to align it to new line MES requirements and Validation Plan, IQ, OQ, PQ Protocol documents · Review IQ, OQ, PQ Task Report and validation plan summary report for MES release and Full eDHR release for different lines and provide support on the approval process. -- *Best Regards,* *Vivek * vi...@deegit.com Hangouts: vivek.recrutier1...@gmail.com Skype: vivekbhargav1299 -- You received this message because you are subscribed to the Google Groups "International SAP Projects" group. To unsubscribe from this group and stop receiving emails from it, send an email to international-sap-projects+unsubscr...@googlegroups.com. To post to this group, send email to international-sap-projects@googlegroups.com. Visit this group at http://groups.google.com/group/international-sap-projects. For more options, visit https://groups.google.com/d/optout.
