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.
- 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
- 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 more than 2 months ago
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