Siemens Opcenter MES Consultant

Overview

On Site
Full Time
Part Time
Accepts corp to corp applications
Contract - W2
Contract - Independent

Skills

XML
MES

Job Details

Job Title: Siemens Opcenter MES Consultant (Medical Device & Diagnostics)

Location: St. Louis, MO

Job Type: Contract (long-term)



Industry: Medical Devices / Manufacturing / Diagnostics

Experience Level: Senior / Lead





Job Description:



We are seeking a skilled Siemens Opcenter MES Consultant with deep expertise in Opcenter Execution for Medical Device and Diagnostics (v8.6 or v2410/v2504). The ideal candidate will possess strong hands-on experience in machine integration, MES configuration, and interfacing with enterprise systems, particularly in regulated GxP environments.





Key Responsibilities:

  • Develop and configure machine integrations using Opcenter Connect MOM with Level 2 systems (OPC UA protocol).
  • Design and implement MES models including UDCD (User Defined Common Data), Business Rules, Expressions, and User Queries.
  • Perform developments in Designer and Portal Studio, including configuration of MAP (XMLs), Workflows, and related components.
  • Configure and support MES SAP interface for seamless data exchange between systems.
  • Generate reports using standard Siemens reporting tools.
  • Collaborate with business analysts and QA teams to create and execute test scripts based on user requirements.
  • Understand and adhere to GxP compliance standards and regulatory requirements within the medical device industry.
  • Analyze existing architecture, identify improvement areas, and propose scalable solutions.

Required Qualifications:

  • Strong hands-on experience with Siemens Opcenter Execution for Medical Device and Diagnostics (v8.6 or v2410/v2504).
  • Expertise in machine integration using Opcenter Connect MOM and OPC UA protocols.
  • Proficiency in modeling MES configurations (UDCD, Business Rules, Expressions, Queries).
  • Experience with Designer and Portal Studio for workflows, MAP (XML) configuration preferred.
  • Familiarity with MES-SAP interfaces and standard Siemens reporting tools preferred.
  • Working knowledge of GxP environments and compliance regulations.
  • Experience in testing: writing and executing test scripts aligned with business requirements.

Soft Skills:

  • Strong problem-solving and analytical thinking.
  • Excellent communication and documentation skills.
  • Collaborative mindset with the ability to work cross-functionally across teams.

Preferred Industry Background:

Medical Devices, Pharmaceuticals, or any regulated manufacturing environments.

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