Siemens OpCenter Developer

Our client seeks an Siemens OpCenter developer for a 12 Months project in Lo Angeles, CA . Below is the detailed requirement Job Title: Siemens OpCenter Develope rWork location : Los Angeles, CA Duration: 12 Months Nature of Jo b: The Siemens Opcenter Developer will design, configure, and deploy MES solutions—primarily Siemens Opcenter (XFP) and Rockwell PharmaSuite—to support compliant manufacturing operations. The developer collaborates closely with manufacturing, quality, engineering, IT, and validation teams to gather requirements and translate them into functional and technical MES designs. Responsibilities include configuring master data, system parameters, and process instructions aligned with GMP-regulated manufacturing workflows. The role also involves developing and testing integrations between MES and enterprise systems such as JDE, LabWare, OSI PI, and plant automation platforms like DeltaV. Compliance with cGMP, FDA, ISPE, and GAMP 5 standards is maintained throughout configuration, development, testing, and troubleshooting activit ies Job Descript ion:Bachelor's degree preferably in Computer Science, Information technology, Computer Engineering, or related IT discipline or equivalent experience with 12+ Minimum Experi • enceMinimum 7+ years working experience in Pharmaceutical/biotech industr • ies.System Integration Experience: JDE, OSIPI, Labware, and De • ltaVMES Platform: Siemens Opcenter Execution Process (formerly known as SIMATIC IT Uni • fiedArchitecture for Process Industries) a plus, CAMSTAR or any other MES System Database Platforms: Microsoft SQL, Oracle, • etc.Project Documentation: Microsoft Of • ficeExperience in MES Implementation, preferably Siemens Opce • nterExperience in FDA regulated industry and familiarity with CFR 21 Part 11, • cGMPTechnical attitude: ability to learn new systems and information quic • kly.Demonstration of in‐depth technical capabilities in system supported manufacturing in a regulated environ mentPrimary Responsibili • tiesDesign, configure, and deploy MES solutions (primarily Siemens Opcenter XFP and Rockwell PharmaSuite)to meet production and compliance requireme • nts.Collaborate with cross‐functional teams, including but, not limited to Manufacturing SME's, Process Engineering, MS, Quality Assurance, Quality Validation, IT, and the respective computerized system teams related to MES interfaces—to gather and analyze business and process requireme • nts.Convert gathered business and process requirements into detailed technical specifications and functional desi • gns.Ensure MES solutions are compliant with applicable industry regulations, including cGMP, FDA, ISPE, and GAMP 5 standa • rds.Design, develop, and implement MES process instructions aligned with manufacturing workflows and business requireme • nts.Set‐up system parameters, master data, and configuration setti • ngs.Implement and manage data synchronization processes to maintain consistency and accuracy across MES and other enterprise sys • temsDevelop and support integration workflows between MES and enterprise systems such as JDE, LabWare, OSI PI, and plant automation equipment (e.g., Delt • aV).Perform comprehensive integration testing to ensure seamless data exchange between MES and connected systems, resolving any issues discovered during test • ing.Analyze existing MES code and scripts to understand system logic and processes and troubleshoot as necess • ary.Contributes to the configuration, development, troubleshooting, and end‐to‐end testing of MES applications and system functionali ties