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    Supply Chain Specialist - San Mateo, United States - Fladger Assoc. Inc.

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    Description

    Job Description

    Job DescriptionSan Dimas, CA/La Verne, CA (Hybrid)Contract Duration: 6-18 monthsRate: Negotiable

    Responsibilities:

    • Excellent employment opportunity for a Supply Chain Specialist I in the San Dimas, CA/La Verne, CA area. Local Candidates ONLY
    • Hybrid role - partial on site and partial possibility of work from home
    • Candidate must meet the Company COVID Vaccine requirement PRIOR to arriving for first day on site.
    • Create and drive completion for Commercial Item Requests and Manufacture requests in GPLM.
    • Drive item extension workflow in EBS for master org and local org set up.
    • Revise formulas in GPLM to support new and ongoing production.
    • Create and revise recipes in EBS to support new and ongoing production.
    • Revise Paper BOM's and checklists in internal company system to support new and ongoing production.
    • Create and drive DCC's to completion in internal company system.
    • Monitor and complete PR tasks to ensure the deadlines are met.
    • Fill out monthly material disposal forms and route for approval in internal company system as required.
    • Works on non-routine problems where analysis of situations or data requires an evaluation of identifiable factors.
    • With guidance exercises independent judgment in developing methods, techniques and evaluation criteria for obtaining results.
    • May provide training and guidance to other Supply Chain personnel.
    • Partners with global master data team to ensure local requirements, processes, and input are considered and incorporated into the implementation of business technology solutions.
    • Executes local master data management processes in line with a global master data governance model.
    • Systems:
      • EBS/Oracle
      • SAP (Future State)
      • MES (Future State)
      • Rapid Response/Kinaxis
      • Microsoft Office Programs

    Experience:

    • 2+ years of relevant experience in related field and a BS or BA; or 1+ year of relevant experience and a MS.
    • Demonstrated high aptitude for working with technical details and data applications required.
    • Strong working knowledge of business enabling software such as MES, SAP, Oracle is highly desired.
    • Experience in Pharmaceutical operations/cGMP environment highly desirable
    • Works on assignments that range from routine to semi routine in nature where independent action and initiative are required in resolving problems and developing recommendations.
    • Works on assignments where ability to recognize deviation from accepted practice is required.
    • Good verbal and written communication skills and interpersonal skills are required.
    • Demonstrates a working knowledge with intermediate level proficiency in Microsoft Office applications.
    • Able to develop solutions to moderately nonroutine problems.
    • Normally receives no instruction on routine work, general instructions on new assignments.
    • Applies working knowledge of manufacturing and production operations and current Good Manufacturing Practices (cGMPs) on a daily basis.



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