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Technical/Sr. Technical MES Consultant

Description
Emerson is actively seeking candidates to fill a Technical/Sr. Technical MES Consultant position to perform and direct the development, design, implementation, testing and delivery of MES Solutions. Technical consultants are key members of a diverse team of professionals executing MES projects in life sciences and related industries. Candidates must have an excellent understanding of key manufacturing processes in the life sciences industry in order to develop and execute the MES strategies used on assigned projects.
A successful Technical/Sr. Technical MES Consultant must be able to quickly develop good working relationships with the Emerson project team members and the client's technical and management personnel. They will participate in all phases of a project from requirements definition through plant startup in a customer facing role. They also must work closely with Project Managers and other technical resources to deliver a successful technical solution that meets the project's requirements for quality, budget, and schedule. Travel to various project sites will be required for requirements gathering, client meetings, engineering support and delivery as required.
Responsibilities
Architect and lead the implementation of Manufacturing Execution System (MES) and system integration solutions projects
Define functional requirements for MES solutions through client interviews and documentation analysis
Develop detailed designs of Syncade MES solutions that meet client requirements
Develop documentation standards for pharma MES projects
Provide project execution leadership and mentor fellow project members
Quickly learn new skills and technologies
Work effectively at different levels within project teams, client organizations and sales
Refine and follow Business Process Maps and/or User Cases for configuration of execution workflows
Develop and improve processes, procedures and tools used in the execution of projects
Work with customers to develop project methodologies that will enhance their standards
Act as a liaison between the internal project team, internal management, and customer project teams and management
Understand the project scope and financials, and participate in the framing and quoting of projects to ensure successful project execution
Plan and organize the work of a project team, develop the implementation strategies for projects, act as a mentor for individuals within the group, and resolve issues within project teams
Identify change orders and justify changes to Project Management; resolve issues and establish priorities between projects
Start-up complex systems at customers' plants
Proactively develop customer relationships; anticipate and provide solutions to customer needs giving high priority to customer satisfaction
Additional Information
Relocation benefits may be available for this position.
Basic Qualifications
BS degree with minimum of 10 years overall experience, with minimum of 10 years MES project experience, and at least 5 years experience working on MES projects in the Pharma industry
Deployment experience with plant floor/Manufacturing Execution Systems (MES) solutions (e.g. Syncade, Rockwell ProPack Data, Werum PAS-X)
Experience with the compliance of the systems and batch record and data integrity
Ability to communicate effectively with customers and employees at different levels of the organization
Excellent verbal and written communication skills in English
Must have the demonstrated ability to work in a team environment as both a leader and an individual contributor
Ability to quickly establish good working relationships with others from all levels
Ability to travel for extended periods of time to project locations for up to 6 to 8 weeks (sometimes several months) with the ability to return home every two weeks
Experience working with customers to create user requirements for MES in the pharma industry.
Experience developing user requirements and Functional Specification documents for MES projects.
Preferred Qualifications
ERP or Quality Systems integration a plus.
Knowledgeable in FDA validation requirements preferred, including: User Requirement and Design Specs, Business Process Procedures, Design Reviews, Requirements gathering,
Experience with regulatory/compliance documentation and procedures is a plus
Experience with .NET technologies preferred
Work Authorization
No calls or agencies please. Emerson will only employ those who are legally authorized to work in the United States. This is a position for which sponsorship may be provided. Individuals with temporary visas such as E, F-1, H-1, H-2, L, B, J, or TN or who need sponsorship for work authorization now or in the future, may be eligible for hire.
Equal Opportunity Employer
Emerson is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to sex, race, color, religion, national origin, age, marital status, political affiliation, sexual orientation, gender identity, genetic information, disability or protected veteran status. We are committed to providing a workplace free of any discrimination or harassment.
If you have a disability and are having difficulty accessing or using this website to apply for a position, you can request help by calling 1-314-553-2544 (V/TTY/TDD) or by sending an email to idisability.administrator@emerson.com.


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