Emerson Process Management isactively seeking candidates to fill a MES Engineer position to perform thedevelopment, design, implementation, testing and delivery of MES Solutions.
Engineers are key members of a diverse team of professionals executing MES projectsin life sciences and related industries.
Candidates must have an excellentunderstanding of key manufacturing processes in the life sciences industry todevelop and execute the MES strategies used on assigned projects.
A successful candidate must beable to quickly develop good working relationships with the Emerson projectteam members and the client’s technical and management personnel.
They willparticipate in all phases of a project from requirements definition throughplant startup in a customer facing role.
They also must work closely withProject Managers and other technical resources to deliver a successfultechnical solution that meets the project’s requirements for quality, budget,and schedule.
Travel to various project sites will be required for requirementsgathering, client meetings, engineering support and delivery as required.
Work withcustomers to develop functional requirements for MES solutions through clientinterviews and documentation analysis.
Developdetailed designs, implement and test Syncade MES solutions that meet clientrequirements.
Developdocumentation required for validated facilities.Quickly learn new skills and technologies.
Workeffectively at different levels within project teams, client organizations andsales.
Identifychange orders and justify changes to Project Lead.
Start-upcomplex systems at customers’ plants.
Proactivelydevelop customer relationships; anticipate and provide solutions to customerneeds giving high priority to customer satisfaction.
Requirements Bachelor’s degree in Chemical Engineering, Electrical, Electronics, Mechatronics or Biomedical Engineering.
3 years of experience in process operations experience in a highly automated pharmaceutical, biotechnology, or similar regulated manufacturing facility subject to Good Manufacturing Practices (GMP) regulations.
Excellent verbal and written communication skills in English.Direct manufacturing or manufacturing support experience in regulated life sciences industry in an automated environment with a demonstrated track record of proficiency.
MES of 3 to 5 years.Experience implementing various functionality in an MES system for Pharmaceutical customersDemonstrated experience of engineering principles related to typical pharmaceutical processing and support equipment.
Syncade and / or Deployment experience with plant floor / Manufacturing Execution Systems (MES) solutions ( Syncade, Rockwell ProPack Data, Werum PAS-
X).Knowledgeable in FDA validation requirements preferred, including : User Requirement and Design Specs, Business Process Procedures, Design Reviews, Requirements gathering,Experience with .
NET technologies preferred.Ability to communicate effectively with customers and employees at different levels of the organization.
Must have the demonstrated ability to work in a team environment.Ability to quickly establish good working relationships with others from all levels.
Travel for short and long periods of time is required.