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 Developer
Work location : Los Angeles, CA
Duration: 12 Months
Nature of Job:
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 activities
Job Description:
Bachelor's degree preferably in Computer Science, Information technology, Computer Engineering, or related IT discipline or equivalent experience with 12+ Minimum Experience
- Minimum 7+ years working experience in Pharmaceutical/biotech industries.
- System Integration Experience: JDE, OSIPI, Labware, and DeltaV
- MES Platform: Siemens Opcenter Execution Process (formerly known as SIMATIC IT Unified
- Architecture for Process Industries) a plus, CAMSTAR or any other MES System Database Platforms: Microsoft SQL, Oracle, etc.
- Project Documentation: Microsoft Office
- Experience in MES Implementation, preferably Siemens Opcenter
- Experience in FDA regulated industry and familiarity with CFR 21 Part 11, cGMP
- Technical attitude: ability to learn new systems and information quickly.
- Demonstration of in‐depth technical capabilities in system supported manufacturing in a regulated environment
Primary Responsibilities
- Design, configure, and deploy MES solutions (primarily Siemens Opcenter XFP and Rockwell PharmaSuite)to meet production and compliance requirements.
- 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 requirements.
- Convert gathered business and process requirements into detailed technical specifications and functional designs.
- Ensure MES solutions are compliant with applicable industry regulations, including cGMP, FDA, ISPE, and GAMP 5 standards.
- Design, develop, and implement MES process instructions aligned with manufacturing workflows and business requirements.
- Set‐up system parameters, master data, and configuration settings.
- Implement and manage data synchronization processes to maintain consistency and accuracy across MES and other enterprise systems
- Develop and support integration workflows between MES and enterprise systems such as JDE, LabWare, OSI PI, and plant automation equipment (e.g., DeltaV).
- Perform comprehensive integration testing to ensure seamless data exchange between MES and connected systems, resolving any issues discovered during testing.
- Analyze existing MES code and scripts to understand system logic and processes and troubleshoot as necessary.
- Contributes to the configuration, development, troubleshooting, and end‐to‐end testing of MES applications and system functionalities
Never miss an opportunity! Create an alert based on the job you applied for.
