Opcenter MES Engineer – Pharma/GxP

US Data Management, LLC

Los Angeles (CA)

Remote

USD 103,320 - 130,872

Full time

14 days+

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Benefits offered by this job

Health, vision, and dental insurance
401k plan participation
Paid time off
Rewards and recognition program

Job summary

US Data Management, LLC is seeking a Siemens Opcenter Developer to design and deploy MES solutions aimed at supporting compliant manufacturing operations. The role involves collaboration with various teams to gather requirements and applying them using Siemens Opcenter and Rockwell PharmaSuite.

This position requires extensive experience in MES implementation, particularly in the pharmaceutical and biotech sectors, ensuring compliance with FDA and cGMP standards. Employees enjoy competitive compensation and comprehensive benefits.

Qualifications

  • Design, configure, and deploy MES solutions aligned with manufacturing workflows.
  • Collaborate with cross-functional teams to gather business and process requirements.
  • Ensure compliance with industry regulations during development and testing.

Responsibilities

  • Design and deploy MES solutions primarily using Siemens Opcenter and Rockwell PharmaSuite.
  • Manage integrations with enterprise systems like JDE, LabWare, and DeltaV.
  • Conduct comprehensive integration testing for seamless data exchange.

Skills

System Integration Experience: JDE, OSIPI, Labware, and DeltaV
MES Platform: Siemens Opcenter Execution Process
Project Documentation: Microsoft Office
Experience in MES Implementation
Minimum 7+ years working experience in Pharmaceutical/biotech industries
Experience in FDA regulated industry
Technical attitude
Demonstration of in-depth technical capabilities

Education

Bachelor’s degree in Computer Science or Information Systems
Master’s Degree preferred

Tools

Microsoft SQL
Oracle

Job description

US Data Management, LLC is seeking a Siemens Opcenter Developer to design and deploy MES solutions aimed at supporting compliant manufacturing operations. The role involves collaboration with various teams to gather requirements and applying them using Siemens Opcenter and Rockwell PharmaSuite.

This position requires extensive experience in MES implementation, particularly in the pharmaceutical and biotech sectors, ensuring compliance with FDA and cGMP standards. Employees enjoy competitive compensation and comprehensive benefits.

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