Supply Chain Specialist - I

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.