MES Consultant

Techtrueup

MES Consultant

Indianapolis, IN
Full Time
Paid
  • Responsibilities

    Job Description

    Position: MES Consultant
    Locations: Indianapolis, IN

    Long-term Contract

    Description

    • Work in partnership with the Global IT team and site representatives to understand business needs and implement innovative solutions to add value to the site while maintaining computer systems in a validated state.
    • Creating Production Procedures using PMX/Syncade/Master Control tool.
    • Testing the Production Procedures in EBR (MES tool) using HP ALM tool.
    • Conduct Process meetings with Business Team.
    • Making the Production Procedure Ticket Valid.
    • Identify and implement technical requirements resulting in appropriate technology, application, process, solution, and information solutions and continually grow depth in one or more technologies, tools, methodologies, and/or concepts.
    • Evaluate and translate functional requirements into technical requirements.
    • Resolve challenging technical issues via break-fix testing, trouble tickets, and/or change requests.
    • Produce and maintain project documentation as required.
    • Exchange technical information with colleagues and onshore/offshore technical resources
    • Support and contribute to the design, development, and delivery of end user training and/or procedures.
    • Assure technology deliverables adhere to company and regulatory policies.
    • Assure technology best practices include use of feedback and monitoring to enhance the state of control of delivered solutions.

    Essential Skills

    • EIS : MES Functional Consulting
    • 6-8 Years’ Experience
    • Experience in Troubleshooting & Resolving issues related to PharmaSuite/PMX/Syncade MES.
    • Working knowledge of IT Life Cycle management, IT Business Process Model, S95 model and other IT processes
    • Excellent communication skills with strong command over written and spoken English.
    • Strong problem-solving, analytical, & process improvement skills.
    • Able to Perform IQ/OQ & develop validation document.
    • Knowledge of Pharmaceutical/Biotech manufacturing processes and/or manufacturing systems
    • Knowledge of MES.
  • Qualifications

    Additional Information

    All your information will be kept confidential according to EEO guidelines.