Position:  MES Consultant



Location: Tampa, FL/Devens, MA



Duration: 12+ Months Contract



 



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/site test and production environments.



Requirements:



10 years minimum experience in Pharmaceuticals/Life Sciences digital manufacturing (GMP/GxP experience)



or



3 years experience with Syncade Manufacturing Execution System (MES) including Recipe Authoring and System Administration



Strong experience in Microsoft Server/Microsoft SQL/VBA



Requirements:



-MES recipe development experience with Emerson-Syncade (5+ years)



-Good understanding of SQL, reporting and SDLC in regulated manufacturing environments in pharmaceutical or biotech industry. (1-2 years)