description

A successful candidate will be familiar with MES computer systems and can manage the activities, schedule and budget for a given project. The role will collaborate on the implementation of systems, coordination of changes and upgrades, improving the digital maturity of a manufacturing plant, and prioritization of business needs at the client site.

Key Responsibilities :

• Manage MES implementation, extension or upgrade projects
• Develop project estimates, plans and approaches to manage end-to end project execution
• Assist customer management in complex tasks such as system architecture and/or business process redesign
• Develop and maintain overall project plan
• Ensure seamless integration into existing processes and systems
• Oversee development and execution of tests
• Plan and schedule training activities for project-teams and end users
• Support or lead validation activities
• Cost controlling (internal as well as customer)
• Ensure timely delivery of the project
• Coordinate subsections of a typical large scale global MES project

Qualifications :

• University degree in a relevant area such as IT, Science, Medical or Engineering
• Knowledge of business processes in pharmaceutical and/or biotech production
• Extensive experience with life science computer systems
• Understanding of the software development life cycle and familiarity with the various phases
• Experience in software deployment in a regulated GMP environment
• Functional understanding of common MES software packages such as Honeywell POMS/POMSnet, Werum PAS-X, Rockwell ProPack Data, Camstar, SAP MES or Emerson Syncade preferred
• Strong quality mindset
• Excellent communication skills
• Readiness to travel to client sites when necessary

Location: Boston, MA

Travel: 40-75% based on client requirements (when it is safe to travel)

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