MES Developer

Found in: Appcast Linkedin GBL C2 - 2 weeks ago


Los Angeles, United States Axial Consulting Inc Full time

At Axial Consulting we redefine possibilities through strategic consulting excellence. As a leading consultancy firm, we specialize in delivering tailored solutions that drive growth, innovation, and transformation for our clients across various industries. Our team of seasoned professionals brings together expertise from diverse backgrounds to tackle complex challenges and uncover opportunities for our clients to thrive in an ever-evolving business landscape.


Role:

  • A client of Axial Consulting is seeking a seasoned MES developer for one of their consulting projects.
  • This is a contract role


Job Functions:

  • Architecting, implementing, and integrating solutions focused on tracking, analyzing, and improving the manufacturing process project(s) in a regulated environment.
  • Designing and implementing data management strategies for the integration of MES solutions with JDE and plant automation equipment (DeltaV).
  • Conceptualizing solutions during the design phase of the project life cycle
  • Manufacturing execution system configuration, programming, debugging, and testing
  • Creating documentation including project design traceability documentation, test cases, and more
  • Leading and guiding cross functional teams from concept to deployment in MES projects of any size
  • Customer facing interaction and technical communication skills.
  • Mentoring colleagues on your expertise and knowledge base


Technology Requirements:

  • ERP Platform: JDE
  • MES Platform: Siemens Opcenter Execution Process (formerly known as SIMATIC IT Unified Architecture for Process Industries)
  • Distributed Control System (DCS): DeltaV
  • Database Platforms: Microsoft SQL, Oracle, etc.
  • Project Documentation: Microsoft Office


Education and Skills Required:

  • Experience in MES Implementation, preferably Siemens Opcenter
  • Minimum 5 years working experience with some or all the listed “Technologies Used”, as mentioned above.
  • Minimum 5 years working experience in Pharmaceutical/biotech industries.
  • 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.
  • Meticulous, conscientious, analytical, focused, self-starter individual.
  • Excellent communication skills – both verbal and written


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