Project MES Lead

Project MES Lead

AutoStream Global are partnering up with multiple global leading pharmaceutical, medical device and biotechnology companies that are looking for a Project MES Lead that can be placed in one of their many sites in Ireland and Europe.

Responsibilities

• This role is to Lead the delivery of an MES project in a pharmaceutical plant in Cork.
• Technical design & delivery lead for MES project within project Automation IT Suite Team
• Work in conjunction with Process Engineers, & operations personal to manage MBR authoring and MBR updates in Werum Paz X for new and upgrade processes.
• Work with enterprise group & MES vendor to create MBR design elements (building blocks) and workflows in Werum PAS-X.
• Ensure technical delivery of MES systems as endorsed by leadership team to meet business objectives.
• Responsible for project oversight and control activities, including definition of scope, requirements & milestone identification, project governance, operational planning, risk identification & mitigation and project closure.
• Responsible for the creation and control of project plans for departmental, cross departmental, and company-wide projects.
• Responsible for ensuring that projects are delivered on time and within budget and scope.
• Delivery of effective & accurate project progress reports.
• Responsible for identification of project risks.
• Oversight & control of project cost management.

Requirements

• Strong MES/IT applications aptitude.
• Good knowledge of MES, in particular Werum PAS-X.
• Bachelor's degree in an engineering discipline with 4 or more years' experience in a technical and/or project management role
• The individual should enjoy working in a dynamic & results oriented team environment where flexibility is essential.
• Excellent Interpersonal Skills - able to express ideas and collaborate effectively with multidisciplinary teams. Be open minded with the ability to recognize good ideas.
• Demonstrated Leadership, Project Management and Engineering experience in MES Introduction in a regulated environment would prove beneficial.
• Will have demonstrated an ability to define project risk and to effectively manage project risks.
• Experience in an FDA regulated or regulated industry beneficial.
• High level of PC Skills required. (MS Excel, Access, PowerPoint, MS Project).
• Experience of GAMP & SDLC
• Working knowledge of SAP would be beneficial.
• Experience with OSI PI Historian
• Experience interfacing MES with automation systems