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MES Consultant

TriOptus LLC

Job Description:

  • Improve and sustain operations at Biologics, Oral Solid Dosage, and Clinical manufacturing plants by supporting on going and future project work.
  • Working directly with manufacturing operations, manufacturing technology, site IT, Quality, and other groups to understand business requirements for corrective actions and continuous improvement initiatives.
  • Create business and technical process maps to reflect the current state and proposed changes.
  • Develop MES solutions including recipe, configuration and/or system changes to meet business requirements.
  • Create and execute system test and/or operational qualification scripts to challenge the business and technical requirements and work with the central and site quality teams for approvals.
  • Support the installation qualification process to migrate recipe, configuration, and associated solution changes from the development to central or site test and production environments.
Requirements:
  • 10 years minimum experience in Pharmaceuticals or Life Sciences digital manufacturing (GMP or GxP experience) or 3 years' experience with Syncade Manufacturing Execution System (MES) including Recipe Authoring and System Administration
  • Strong experience in Microsoft Server or Microsoft SQL/VBA
Skills:
  • Advanced Computer Skills: 6 to 10 years
  • Automation Systems: 6 to 10 years
  • Basic Programming: 6 to 10 years
  • Good Manufacturing Practices (GMP): 6 to 10 years
  • SQL: 6 to 10 years
  • Syncade MES (Manufacturing Execution System): 6 to 10 years
Vacancy posted 5 days ago
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