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Jobs or company...
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MES Engineer

  • Full Time, onsite
  • PharmEng Technology Americas
  • On Site, United States of America
Salary undisclosed

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Job Description

Job Description

PharmEng Technology is seeking an experienced MES Application Engineer for a project in Houston Texas to help drive our solution-based business model and take our designs to the next level. The MES Application Engineer is responsible for supporting activities such as requirements gathering, definition, and application/test/implementation of Manufacturing Execution System (MES) client projects; primarily, but not limited to, the pharmaceutical/biotech industries.

Job Responsibilities:

  • Responsible for execution of protocols for testing and validating electronic batch records.
  • Responsible for testing of MES systems project, which includes infrastructure setup, software installation, recipe development, and System Acceptance Testing (SAT) with users.
  • Working with MES leads, system users and process owners to develop, revise and maintain MES recipes.
  • Responsible for creating and maintaining electronic logbooks and electronic batch records.
  • Responsible for creating and maintaining electronic batch records and configuring production recipes using object libraries.
  • The potential resource should be capable of driving the testing and deployment of Opcenter software solutions, ensuring sufficient automated testing to maintain solution quality.
  • The potential resource must have experience with Electronic Batch Record System Modeling specifically in the Siemens Opcenter platform.
  • Responsible for assisting in designing and deployment of MES systems to replace paper-based or manual systems including batch records, weigh & dispense, warehouse management and material tracking in a pharmaceutical or medical device environment.
  • Actively participate in fit-gap analysis of customer requirements vs. MES system functionality.
  • Provide technical input to help troubleshoot issues during MES usage and support end-users in MES navigation, EBR execution and general system utilization to ensure users become self-sufficient.
  • Practical hands-on experience with Siemens Opcenter is required.
  • The potential resource should have experience in gathering requirements and translating them into a product vision, demonstrating expertise in development and engineering.
  • Experience in application development, testing, and support based on the Software Development Life Cycle (SDLC) methodology is necessary. Demonstrated understanding of key pharmaceutical niche processes, Pharma GxP regulations, and ISA-88/ISA-95 standards is important in this role.

Job Requirements:

  • Bachelor s Degree in Engineering/Computer Science/Integrated Manufacturing disciplines or equivalent experience.
  • Firm understanding of cGMP validation requirements/guidelines and current industry practice.
  • More than 4 years of working experience with JAVA, Oracle, C, C++and SQL.
  • More than 4 years of working experience with SAP and ERP.
  • More than 4 years of working experience with Werum PAS-X, Syncade, and Aspen Tech.
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
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