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Fremont

    Documentation Specialist III - Fremont, United States - Compunnel Inc.

    Default job background
    Pharmaceutical / Bio-tech
    Description

    Documentation Specialist III / AutoCAD

    Duties:

    • The US Biopharma E&T (Engineering & Technology) Department is seeking a service partner to support revisions to our Facility and Engineering Drawings and Documentation database.
    • These drawings are very critical to the site for design and maintenance activities.
    • The drawings are maintained electronically in our CAD (Computer Aided Design) database.
    • The department has a fluctuating amount of CAD work in support, driven by facility changes (CapEx projects), ranging from a few hours per week, to 40-60 hours at peak demand.
    • Engaging an external partner with the necessary technical capabilities would allow the organization to address demand flexibly.

    Work Description:

    • Perform requested updates to Engineering Drawings
    • Make changes to engineering drawings using AutoDesk AutoCAD or other drafting/modeling programs, to the specifications of the drawing project or redline documents.
    • Maintain drawings in the Engineering Drawing Management System (EDMS)
    • Download, upload, update, start/complete tasks and otherwise maintain drawings and data in the EDMS system. (Specifically, Siemens COMOS)
    • Maintains and Completes Work Orders in task management system (MAXIMO)
    • Work Order tracking at is accomplished via the "Maximo" application and requires some manual input.
    • Complete requested work in a timely manner
    • Maintain Open communication with Engineering Documentation
    • Intellectual property

    Requirements:

    • Maintenance of a network account
    • Continuous on-time completion of all assigned training
    • Computing Equipment
    • Collaboration
    • Works under minimal technical supervision
    • Work location
    • Task Management
    • Work hours
    • Ability to travel to site on same-day notice
    • Training

    Skills:

    • Expert knowledge in AutoCAD and design
    • Site facility knowledge
    • Experience in GMP manufacturing facilities
    • An ability to read, understand and modify Engineering drawings, including P&ID's

    Education:

    • Bachelor's Degree in Engineering
    • Three to five years of experience in related Life Science industry
    • Good knowledge and understanding of biopharmaceutical industry and AutoCAD experience


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